236 Publikationen

Alle markieren

[236]
2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2936254
Isolation and characterization of side-products formed through ∆2-isomerization in the synthesis of cefpodoxime proxetil.
Pieper, Matthias, Isolation and characterization of side-products formed through ∆2-isomerization in the synthesis of cefpodoxime proxetil.. The Journal of antibiotics (). , 2019
PUB | DOI | PubMed | Europe PMC
 
[235]
2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2936145
Cyanide-free synthesis of an aromatic nitrile from a biorenewable-based aldoxime: Development and application of a recombinant aldoxime dehydratase as a biocatalyst
Choi, Ji-Eun, Cyanide-free synthesis of an aromatic nitrile from a biorenewable-based aldoxime: Development and application of a recombinant aldoxime dehydratase as a biocatalyst. BIOCATALYSIS AND BIOTRANSFORMATION (). , 2019
PUB | DOI | WoS
 
[234]
2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2935493
Asymmetric Formal Synthesis of (+)-Catharanthine via Desymmetrization of Isoquinuclidine.
Kono, Masato, Asymmetric Formal Synthesis of (+)-Catharanthine via Desymmetrization of Isoquinuclidine.. Organic letters 21 (10). , 2019
PUB | DOI | WoS | PubMed | Europe PMC
 
[233]
2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2935205
Chemoenzymatic Synthesis of a Chiral Ozanimod Key Intermediate Starting from Naphthalene as Cheap Petrochemical Feedstock.
Uthoff, Florian, Chemoenzymatic Synthesis of a Chiral Ozanimod Key Intermediate Starting from Naphthalene as Cheap Petrochemical Feedstock.. The Journal of organic chemistry 84 (8). , 2019
PUB | DOI | WoS | PubMed | Europe PMC
 
[232]
2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2933178
Biocatalytic Reduction of 2-Monosubstituted 3-Thiazolines Using Imine Reductases
Zumbrägel, Nadine, Biocatalytic Reduction of 2-Monosubstituted 3-Thiazolines Using Imine Reductases. Journal of Heterocyclic Chemistry (). , 2019
PUB | DOI | WoS
 
[231]
2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2934545
Detection and fragmentation of doubly charged peptide ions in MALDI-Q-TOF-MS by ion mobility spectrometry for improved protein identification.
Sproß, Jens, Detection and fragmentation of doubly charged peptide ions in MALDI-Q-TOF-MS by ion mobility spectrometry for improved protein identification.. Analytical and bioanalytical chemistry (). , 2019
PUB | DOI | PubMed | Europe PMC
 
[230]
2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2934606
Catalysts Encapsulated in Biopolymer Hydrogels for Chemoenzymatic One-Pot Processes in Aqueous Media
Pauly, Jan, Catalysts Encapsulated in Biopolymer Hydrogels for Chemoenzymatic One-Pot Processes in Aqueous Media. CHEMCATCHEM 11 (5). , 2019
PUB | DOI | WoS
 
[229]
2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2934607
Enantioselective One-Pot Synthesis of Biaryl-Substituted Amines by Combining Palladium and Enzyme Catalysis in Deep Eutectic Solvents
Paris, Juraj, Enantioselective One-Pot Synthesis of Biaryl-Substituted Amines by Combining Palladium and Enzyme Catalysis in Deep Eutectic Solvents. ACS SUSTAINABLE CHEMISTRY & ENGINEERING 7 (5). , 2019
PUB | DOI | WoS
 
[228]
2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2933685
Type II flavoprotein monooxygenase PsFMO_A from the bacterium Pimelobacter sp. Bb-B catalyzes enantioselective Baeyer-Villiger oxidations with a relaxed cofactor specificity.
Löwe, Jana, Type II flavoprotein monooxygenase PsFMO_A from the bacterium Pimelobacter sp. Bb-B catalyzes enantioselective Baeyer-Villiger oxidations with a relaxed cofactor specificity.. Journal of biotechnology (). , 2019
PUB | DOI | WoS | PubMed | Europe PMC
 
[227]
2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2934376
An Asymmetric Organocatalytic Aldol Reaction of a Hydrophobic Aldehyde in Aqueous Medium Running in Flow Mode
Schober, Lukas, An Asymmetric Organocatalytic Aldol Reaction of a Hydrophobic Aldehyde in Aqueous Medium Running in Flow Mode. SYNTHESIS-STUTTGART 51 (5). , 2019
PUB | DOI | WoS
 
[226]
2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2934122
Amine Transaminase from Exophiala Xenobiotica-Crystal Structure and Engineering of a Fold IV Transaminase that Naturally Converts Biaryl Ketones
Telzerow, Aline, Amine Transaminase from Exophiala Xenobiotica-Crystal Structure and Engineering of a Fold IV Transaminase that Naturally Converts Biaryl Ketones. ACS CATALYSIS 9 (2). , 2019
PUB | DOI | WoS
 
[225]
2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2933300
Biocatalytic concepts for synthesizing amine bulk chemicals: recent approaches towards linear and cyclic aliphatic primary amines and substituted derivatives thereof
Gröger, Harald, Biocatalytic concepts for synthesizing amine bulk chemicals: recent approaches towards linear and cyclic aliphatic primary amines and substituted derivatives thereof. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY 103 (1). , 2019
PUB | DOI | WoS | PubMed | Europe PMC
 
[224]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2921159
Providing reducing power by microalgal photosynthesis: a novel perspective towards sustainable biocatalytic production of bulk chemicals exemplified for aliphatic amines
Löwe, Jana, Providing reducing power by microalgal photosynthesis: a novel perspective towards sustainable biocatalytic production of bulk chemicals exemplified for aliphatic amines. Scientific Reports 8 (1). , 2018
PUB | PDF | DOI | WoS | PubMed | Europe PMC
 
[223]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2932504
Biocatalytic production of adiponitrile and related aliphatic linear α,ω-dinitriles
Betke, Tobias, Biocatalytic production of adiponitrile and related aliphatic linear α,ω-dinitriles. Nature Communications 9 (). , 2018
PUB | PDF | DOI | WoS | PubMed | Europe PMC
 
[222]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2930227
Merging Heterocyclic Chemistry and Biocatalysis in One-Pot Processes through Compartmentalization of the Reaction Steps
Zumbrägel, Nadine, Merging Heterocyclic Chemistry and Biocatalysis in One-Pot Processes through Compartmentalization of the Reaction Steps. Bioengineering 5 (). , 2018
PUB | PDF | DOI | PubMed | Europe PMC
 
[221]
2018 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2933180
Chiral Dinuclear Vanadium Complex-Mediated Oxidative Coupling of Resorcinols
Sako, Makoto, Chiral Dinuclear Vanadium Complex-Mediated Oxidative Coupling of Resorcinols. The Journal of Organic Chemistry (). , 2018
PUB | DOI | WoS | PubMed | Europe PMC
 
[220]
2018 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2933177
Enantioselective Biocatalytic Reduction of 2H-1,4-Benzoxazines Using Imine Reductases
Zumbrägel, Nadine, Enantioselective Biocatalytic Reduction of 2H-1,4-Benzoxazines Using Imine Reductases. The Journal of Organic Chemistry (). , 2018
PUB | DOI | WoS | PubMed | Europe PMC
 
[219]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2933928
The function of the oxylipin 12-oxophytodienoic acid in cell signaling, stress acclimation, and development
Maynard, Daniel, The function of the oxylipin 12-oxophytodienoic acid in cell signaling, stress acclimation, and development. JOURNAL OF EXPERIMENTAL BOTANY 69 (22). , 2018
PUB | DOI | WoS | PubMed | Europe PMC
 
[218]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2933179
One-pot synthesis of a 3-thiazolidine through combination of an Asinger-type multi-component-condensation reaction with an enzymatic imine reduction
Zumbrägel, Nadine, One-pot synthesis of a 3-thiazolidine through combination of an Asinger-type multi-component-condensation reaction with an enzymatic imine reduction. Journal of Biotechnology 291 (). , 2018
PUB | DOI | WoS | PubMed | Europe PMC
 
[217]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2932766
Metathesis in water conducted by tailor-made encapsulated Grubbs' catalyst
Pauly, Jan, Metathesis in water conducted by tailor-made encapsulated Grubbs' catalyst. GREEN CHEMISTRY 20 (22). , 2018
PUB | DOI | WoS
 
[216]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2919867
Enantioselective reduction of sulfur-containing cyclic imines through biocatalysis
Zumbrägel, Nadine, Enantioselective reduction of sulfur-containing cyclic imines through biocatalysis. Nature Communications 9 (). , 2018
PUB | DOI | WoS | PubMed | Europe PMC
 
[215]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2931977
Novel Insights into the Combination of Metal- and Biocatalysis: Cascade One-Pot Synthesis of Enantiomerically Pure Biaryl Alcohols in Deep Eutectic Solvents
Paris, Juraj, Novel Insights into the Combination of Metal- and Biocatalysis: Cascade One-Pot Synthesis of Enantiomerically Pure Biaryl Alcohols in Deep Eutectic Solvents. CHEMCATCHEM 10 (19). , 2018
PUB | DOI | WoS
 
[214]
2018 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2920724
Design, characterisation and application of alginate-based encapsulated pig liver esterase
Pauly, Jan, Design, characterisation and application of alginate-based encapsulated pig liver esterase. Journal of Biotechnology 280 (). , 2018
PUB | Dateien verfügbar | DOI | WoS | PubMed | Europe PMC
 
[213]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2931244
Stereoselective synthesis of enantiomerically pure bowl-shaped hydroxytribenzotriquinacenes
Rommelmann, Philipp, Stereoselective synthesis of enantiomerically pure bowl-shaped hydroxytribenzotriquinacenes. ORGANIC & BIOMOLECULAR CHEMISTRY 16 (31). , 2018
PUB | DOI | WoS | PubMed | Europe PMC
 
[212]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2931119
Process Development for Synthesizing the Cephalosporin Antibiotic Cefotaxime in Batch and Flow Mode
Pieper, Matthias, Process Development for Synthesizing the Cephalosporin Antibiotic Cefotaxime in Batch and Flow Mode. ORGANIC PROCESS RESEARCH & DEVELOPMENT 22 (8). , 2018
PUB | DOI | WoS
 
[211]
2018 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2930305
Vanadium-Catalyzed Dehydrogenation of N-Heterocycles in Water
Zumbrägel, Nadine, Vanadium-Catalyzed Dehydrogenation of N-Heterocycles in Water. Organic Letters 20 (16). , 2018
PUB | DOI | WoS | PubMed | Europe PMC
 
[210]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2931113
Asymmetric Synthesis of 1-Phenylethylamine from Styrene via Combined Wacker Oxidation and Enzymatic Reductive Amination
Uthoff, Florian, Asymmetric Synthesis of 1-Phenylethylamine from Styrene via Combined Wacker Oxidation and Enzymatic Reductive Amination. JOURNAL OF ORGANIC CHEMISTRY 83 (16). , 2018
PUB | DOI | WoS | PubMed | Europe PMC
 
[209]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920277
Enantioselective synthesis of amines via reductive amination with a dehydrogenase mutant from Exigobacterium sibiricum: Substrate scope, co-solvent tolerance and biocatalyst immobilization
Löwe, Jana, Enantioselective synthesis of amines via reductive amination with a dehydrogenase mutant from Exigobacterium sibiricum: Substrate scope, co-solvent tolerance and biocatalyst immobilization. BIOORGANIC & MEDICINAL CHEMISTRY 26 (7). , 2018
PUB | DOI | WoS | PubMed | Europe PMC
 
[208]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2913715
One-pot synthesis of bioactive cyclopentenones from α-linolenic acid and docosahexaenoic acid
Maynard, Daniel, One-pot synthesis of bioactive cyclopentenones from α-linolenic acid and docosahexaenoic acid. Bioorganic & Medicinal Chemistry 26 (7). , 2018
PUB | DOI | WoS | PubMed | Europe PMC
 
[207]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916923
Biocatalytic Synthesis of Nitriles through Dehydration of Aldoximes: The Substrate Scope of Aldoxime Dehydratases
Betke, Tobias, Biocatalytic Synthesis of Nitriles through Dehydration of Aldoximes: The Substrate Scope of Aldoxime Dehydratases. ChemBioChem 19 (8). , 2018
PUB | DOI | WoS | PubMed | Europe PMC
 
[206]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2919325
Opportunities and challenges for combining chemo- and biocatalysis
Rudroff, Florian, Opportunities and challenges for combining chemo- and biocatalysis. NATURE CATALYSIS 1 (1). , 2018
PUB | DOI | WoS
 
[205]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2913114
Cyanide-Free and Broadly Applicable Enantioselective Synthetic Platform for Chiral Nitriles through a Biocatalytic Approach
Betke, Tobias, Cyanide-Free and Broadly Applicable Enantioselective Synthetic Platform for Chiral Nitriles through a Biocatalytic Approach. Angewandte Chemie (International ed. in English) 46 (40). , 2017
PUB | DOI | WoS | PubMed | Europe PMC
 
[204]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916530
Industrial landmarksinthedevelopmentofsustainableproduction processesforthe beta-lactam antibiotickeyintermediate 7-aminocephalosporanic acid (7-ACA)
Gröger, Harald, Industrial landmarksinthedevelopmentofsustainableproduction processesforthe beta-lactam antibiotickeyintermediate 7-aminocephalosporanic acid (7-ACA). SUSTAINABLE CHEMISTRY AND PHARMACY 5 (). , 2017
PUB | DOI | WoS
 
[203]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2910386
Process Development through Solvent Engineering in the Biocatalytic Synthesis of the Heterocyclic Bulk Chemical epsilon-Caprolactone
Reimer, Anna, Process Development through Solvent Engineering in the Biocatalytic Synthesis of the Heterocyclic Bulk Chemical epsilon-Caprolactone. JOURNAL OF HETEROCYCLIC CHEMISTRY 54 (1). , 2017
PUB | DOI | WoS
 
[202]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2911773
"Side-Product Catalysis": Substrate Autoxidation as an Overlooked Side Reaction Generating a Co-Catalyst for Enhancing Asymmetric Aldol Reactions
Heidlindemann, Marcel, "Side-Product Catalysis": Substrate Autoxidation as an Overlooked Side Reaction Generating a Co-Catalyst for Enhancing Asymmetric Aldol Reactions. CHEMCATCHEM 9 (8). , 2017
PUB | DOI | WoS
 
[201]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909081
First Tandem-Type One-Pot Process Combining Asymmetric Organo- and Biocatalytic Reactions in Aqueous Media Exemplified for the Enantioselective and Diastereoselective Synthesis of 1,3-Diols
Rulli, Giuseppe, First Tandem-Type One-Pot Process Combining Asymmetric Organo- and Biocatalytic Reactions in Aqueous Media Exemplified for the Enantioselective and Diastereoselective Synthesis of 1,3-Diols. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY 2017 (4). , 2017
PUB | DOI | WoS
 
[200]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2908557
Recombinant expression and characterization of a l-amino acid oxidase from the fungus Rhizoctonia solani
Hahn, Katharina, Recombinant expression and characterization of a l-amino acid oxidase from the fungus Rhizoctonia solani. Applied Microbiology and Biotechnology 101 (7). , 2017
PUB | DOI | WoS | PubMed | Europe PMC
 
[199]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2910338
An alternative approach towards poly-epsilon-caprolactone through a chemoenzymatic synthesis: combined hydrogenation, bio-oxidations and polymerization without the isolation of intermediates
Wedde, Severin, An alternative approach towards poly-epsilon-caprolactone through a chemoenzymatic synthesis: combined hydrogenation, bio-oxidations and polymerization without the isolation of intermediates. GREEN CHEMISTRY 19 (5). , 2017
PUB | DOI | WoS
 
[198]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2910354
Formal Enantioselective Hydroamination of Non-Activated Alkenes: Transformation of Styrenes into Enantiomerically Pure 1-Phenylethylamines in Chemoenzymatic One-Pot Synthesis
Uthoff, Florian, Formal Enantioselective Hydroamination of Non-Activated Alkenes: Transformation of Styrenes into Enantiomerically Pure 1-Phenylethylamines in Chemoenzymatic One-Pot Synthesis. CHEMCATCHEM 9 (4). , 2017
PUB | DOI | WoS
 
[197]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2908777
Kinetic insights into ϵ-caprolactone synthesis: Improvement of an enzymatic cascade reaction
Scherkus, Christian, Kinetic insights into ϵ-caprolactone synthesis: Improvement of an enzymatic cascade reaction. Biotechnology and Bioengineering 114 (6). , 2017
PUB | DOI | WoS | PubMed | Europe PMC
 
[196]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916529
Enzymatic resolution of an amine under solvent-free conditions with diethyl malonate as reagent for acylation
Uthoff, Florian, Enzymatic resolution of an amine under solvent-free conditions with diethyl malonate as reagent for acylation. SUSTAINABLE CHEMISTRY AND PHARMACY 5 (). , 2017
PUB | DOI | WoS
 
[195]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2914659
High-throughput-feasible screening tool for determining enzyme stabilities against organic solvents directly from crude extracts
Wedde, Severin, High-throughput-feasible screening tool for determining enzyme stabilities against organic solvents directly from crude extracts. Chembiochem : a European journal of chemical biology 18 (24). , 2017
PUB | DOI | WoS | PubMed | Europe PMC
 
[194]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2912688
ASYMMETRIC BIOCATALYTIC REDUCTION OF CYCLIC IMINES: DESIGN AND APPLICATION OF A TAILOR-MADE WHOLE-CELL CATALYST
Zumbrägel, Nadine, ASYMMETRIC BIOCATALYTIC REDUCTION OF CYCLIC IMINES: DESIGN AND APPLICATION OF A TAILOR-MADE WHOLE-CELL CATALYST. HETEROCYCLES 95 (2). , 2017
PUB | DOI | WoS
 
[193]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916457
Synthesis of Enantiomerically Pure N-Acyl Amino Nitriles via Catalytic Dehydration of Oximes and Application in a de Novo Synthesis of Vildagliptin
Rommelmann, Philipp, Synthesis of Enantiomerically Pure N-Acyl Amino Nitriles via Catalytic Dehydration of Oximes and Application in a de Novo Synthesis of Vildagliptin. Organic Process Research & Development 21 (10). , 2017
PUB | DOI | WoS
 
[192]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909084
Design of recombinant whole-cell catalysts for double reduction of C=C and C=O bonds in enals and application in the synthesis of Guerbet alcohols as industrial bulk chemicals for lubricants
Biermann, Marc, Design of recombinant whole-cell catalysts for double reduction of C=C and C=O bonds in enals and application in the synthesis of Guerbet alcohols as industrial bulk chemicals for lubricants. GREEN CHEMISTRY 19 (2). , 2017
PUB | DOI | WoS
 
[191]
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2904890
Screening, Molecular Cloning, and Biochemical Characterization of an Alcohol Dehydrogenase from Pichia pastoris Useful for the Kinetic Resolution of a Racemic β-Hydroxy-β-trifluoromethyl Ketone
Bulut, Dalia, Screening, Molecular Cloning, and Biochemical Characterization of an Alcohol Dehydrogenase from Pichia pastoris Useful for the Kinetic Resolution of a Racemic β-Hydroxy-β-trifluoromethyl Ketone. Chembiochem 17 (14). , 2016
PUB | DOI | WoS | PubMed | Europe PMC
 
[190]
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2907316
A whole cell biocatalyst for double oxidation of cyclooctane
Müller, C. A., A whole cell biocatalyst for double oxidation of cyclooctane. Journal of Industrial Microbiology & Biotechnology 43 (12). , 2016
PUB | DOI | WoS | PubMed | Europe PMC
 
[189]
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2906851
A One-Pot Cascade Reaction Combining an Encapsulated Decarboxylase with a Metathesis Catalyst for the Synthesis of Bio-Based Antioxidants
Gómez Baraibar, Álvaro, A One-Pot Cascade Reaction Combining an Encapsulated Decarboxylase with a Metathesis Catalyst for the Synthesis of Bio-Based Antioxidants. Angewandte Chemie International Edition 55 (47). , 2016
PUB | DOI | WoS | PubMed | Europe PMC
 
[188]
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2906192
Shibasaki Catalysts and Their Use for Asymmetric Synthetic Applications by the Chemical Industry
Gröger, Harald, Shibasaki Catalysts and Their Use for Asymmetric Synthetic Applications by the Chemical Industry. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY (24). , 2016
PUB | DOI | WoS
 
[187]
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2917152
Guerbet Alcohols: From Processes under Harsh Conditions to Synthesis at Room Temperature under Ambient Pressure
Biermann, Marc, Guerbet Alcohols: From Processes under Harsh Conditions to Synthesis at Room Temperature under Ambient Pressure. CHEMCATCHEM 8 (5). , 2016
PUB | DOI | WoS
 
[186]
2016 | Konferenzbeitrag | Veröffentlicht | PUB-ID: 2908647
Nano/Microfluidic Devices for Whole-Cell Biocatalyst Analysis by UV/VIS-Spectroscopy
Viefhues, Martina, Nano/Microfluidic Devices for Whole-Cell Biocatalyst Analysis by UV/VIS-Spectroscopy. Proceedings of the 20. International Conference on Miniaturized Systems for Chemistry and Life Sciences 2016 (µTAS 2016) (). Dublin, Irland, 2016
PUB
 
[185]
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2907726
A Fed-Batch Synthetic Strategy for a Three-Step Enzymatic Synthesis of Poly-epsilon-caprolactone
Scherkus, Christian, A Fed-Batch Synthetic Strategy for a Three-Step Enzymatic Synthesis of Poly-epsilon-caprolactone. CHEMCATCHEM 8 (22). , 2016
PUB | DOI | WoS
 
[184]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2785615
Olefin Metathesis Reaction in Water and in Air Improved by Supramolecular Additives
Tomasek, Jasmine, Olefin Metathesis Reaction in Water and in Air Improved by Supramolecular Additives. Molecules 20 (10). , 2015
PUB | DOI | WoS | PubMed | Europe PMC
 
[183]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2901254
Biocatalytic access to chiral polyesters by an artificial enzyme cascade synthesis
Schmidt, Sandy, Biocatalytic access to chiral polyesters by an artificial enzyme cascade synthesis. ChemCatChem 7 (23). , 2015
PUB | DOI | WoS
 
[182]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2773289
Synthesis of substituted cycloalkene-1,1-dicarboxylates via olefin metathesis in water
Tenbrink, Katharina, Synthesis of substituted cycloalkene-1,1-dicarboxylates via olefin metathesis in water. ARKIVOC (). , 2015
PUB | DOI | WoS
 
[181]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2764353
Integrated Biocatalysis in Multistep Drug Synthesis without Intermediate Isolation: A de Novo Approach toward a Rosuvastatin Key Building Block
Metzner, Richard, Integrated Biocatalysis in Multistep Drug Synthesis without Intermediate Isolation: A de Novo Approach toward a Rosuvastatin Key Building Block. Organic Process Research & Development 19 (6). , 2015
PUB | DOI | WoS
 
[180]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2719049
Iron(III)-porphyrin Complex FeTSPP: A Versatile Water-soluble Catalyst for Oxidations in Organic Syntheses, Biorenewables Degradation and Environmental Applications
Böhm, Philipp, Iron(III)-porphyrin Complex FeTSPP: A Versatile Water-soluble Catalyst for Oxidations in Organic Syntheses, Biorenewables Degradation and Environmental Applications. ChemCatChem 7 (1). , 2015
PUB | DOI | WoS
 
[179]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2757961
Vanadium in asymmetric synthesis: emerging concepts in catalyst design and applications
Takizawa, Shinobu, Vanadium in asymmetric synthesis: emerging concepts in catalyst design and applications. Chemistry 21 (25). , 2015
PUB | DOI | WoS | PubMed | Europe PMC
 
[178]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2721884
An Enzyme Cascade Synthesis of ε-Caprolactone and its Oligomers
Schmidt, Sandy, An Enzyme Cascade Synthesis of ε-Caprolactone and its Oligomers. Angewandte Chemie (International ed. in English) 54 (9). , 2015
PUB | DOI | WoS | PubMed | Europe PMC
 
[177]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2729781
Cooperative Catalysis of Noncompatible Catalysts through Compartmentalization: Wacker Oxidation and Enzymatic Reduction in a One-Pot Process in Aqueous Media
Sato, Hirofumi, Cooperative Catalysis of Noncompatible Catalysts through Compartmentalization: Wacker Oxidation and Enzymatic Reduction in a One-Pot Process in Aqueous Media. Angewandte Chemie (International ed. in English) 54 (15). , 2015
PUB | DOI | WoS | PubMed | Europe PMC
 
[176]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2786832
Enantiomerically Pure Tribenzotriquinacenes through Stereoselective Synthesis
Greschner, Wilko, Enantiomerically Pure Tribenzotriquinacenes through Stereoselective Synthesis. Angewandte Chemie (International ed. in English) 54 (46). , 2015
PUB | DOI | WoS | PubMed | Europe PMC
 
[175]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2773287
Professor Dr. Jürgen Martens A tribute
Gröger, Harald, Professor Dr. Jürgen Martens A tribute. ARKIVOC (). , 2015
PUB | WoS
 
[174]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2758474
The Organic-Synthetic Potential of Recombinant Ene Reductases: Substrate-Scope Evaluation and Process Optimization
Reß, Tina, The Organic-Synthetic Potential of Recombinant Ene Reductases: Substrate-Scope Evaluation and Process Optimization. ChemCatChem 7 (8). , 2015
PUB | DOI | WoS
 
[173]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2761249
Development of a growth-dependent selection system for identification of L-threonine aldolases
Bulut, Dalia, Development of a growth-dependent selection system for identification of L-threonine aldolases. Applied Microbiology and Biotechnology 99 (14). , 2015
PUB | DOI | WoS | PubMed | Europe PMC
 
[172]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2729792
Chemoenzymatic Synthesis of Vitamin B5-Intermediate (R)-Pantolactone via Combined Asymmetric Organo- and Biocatalysis
Heidlindemann, Marcel, Chemoenzymatic Synthesis of Vitamin B5-Intermediate (R)-Pantolactone via Combined Asymmetric Organo- and Biocatalysis. The Journal of Organic Chemistry 80 (7). , 2015
PUB | DOI | WoS | PubMed | Europe PMC
 
[171]
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2690890
Combination of Asymmetric Organo- and Biocatalytic Reactions in Organic Media Using Immobilized Catalysts in Different Compartments
Heidlindemann, Marcel, Combination of Asymmetric Organo- and Biocatalytic Reactions in Organic Media Using Immobilized Catalysts in Different Compartments. ACS Catalysis 4 (4). , 2014
PUB | DOI | WoS
 
[170]
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2707682
Cyanide-free Enantioselective Synthesis of Nitriles: Synthetic Proof of a Biocatalytic Concept and Mechanistic Insights
Metzner, Richard, Cyanide-free Enantioselective Synthesis of Nitriles: Synthetic Proof of a Biocatalytic Concept and Mechanistic Insights. ChemCatChem 6 (11). , 2014
PUB | DOI | WoS
 
[169]
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2708851
Strategies for regeneration of nicotinamide coenzymes emphasizing self-sufficient closed-loop recycling systems
Hummel, Werner, Strategies for regeneration of nicotinamide coenzymes emphasizing self-sufficient closed-loop recycling systems. Journal of biotechnology 191 (). , 2014
PUB | DOI | WoS | PubMed | Europe PMC
 
[168]
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2708863
Whole-cell double oxidation of n-heptane
Müller, Christina A., Whole-cell double oxidation of n-heptane. Journal of biotechnology 191 (). , 2014
PUB | DOI | WoS | PubMed | Europe PMC
 
[167]
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2681761
Artificial cofactor regeneration with an iron(III)porphyrin as NADH-oxidase mimic in the enzymatic oxidation of L-glutamate to alpha-ketoglutarate
Greschner, Wilko, Artificial cofactor regeneration with an iron(III)porphyrin as NADH-oxidase mimic in the enzymatic oxidation of L-glutamate to alpha-ketoglutarate. Journal of Molecular Catalysis B Enzymatic 103 (). , 2014
PUB | DOI | WoS
 
[166]
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2699267
Enzymatic resolution of racemates with a 'remote' stereogenic center as an efficient tool in drug, flavor and vitamin synthesis
Alfaro Blasco, Maria, Enzymatic resolution of racemates with a 'remote' stereogenic center as an efficient tool in drug, flavor and vitamin synthesis. Bioorganic & medicinal chemistry 22 (20). , 2014
PUB | DOI | WoS | PubMed | Europe PMC
 
[165]
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2682298
Combining the 'two worlds' of chemocatalysis and biocatalysis towards multi-step one-pot processes in aqueous media
Gröger, Harald, Combining the 'two worlds' of chemocatalysis and biocatalysis towards multi-step one-pot processes in aqueous media. Current opinion in chemical biology 19 (). , 2014
PUB | DOI | WoS | PubMed | Europe PMC
 
[164]
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2677387
Enantioselective Rearrangement Coupled with Water Addition: Direct Synthesis of Enantiomerically Pure Saturated Carboxylic Acids from a, b- Unsaturated Aldehydes
Winkler, Till, Enantioselective Rearrangement Coupled with Water Addition: Direct Synthesis of Enantiomerically Pure Saturated Carboxylic Acids from a, b- Unsaturated Aldehydes. ChemCatChem 6 (4). , 2014
PUB | DOI | WoS
 
[163]
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2672840
Hydroxy Functionalization of Non-Activated C-H and C=C Bonds: New Perspectives for the Synthesis of Alcohols through Biocatalytic Processes
Gröger, Harald, Hydroxy Functionalization of Non-Activated C-H and C=C Bonds: New Perspectives for the Synthesis of Alcohols through Biocatalytic Processes. Angewandte Chemie. International edition 53 (12). , 2014
PUB | DOI | WoS | PubMed | Europe PMC
 
[162]
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2621177
Direct biocatalytic one-pot-transformation of cyclohexanol with molecular oxygen into ɛ-caprolactone
Staudt, Svenja, Direct biocatalytic one-pot-transformation of cyclohexanol with molecular oxygen into ɛ-caprolactone. Enzyme and microbial technology 53 (4). , 2013
PUB | DOI | WoS | PubMed | Europe PMC
 
[161]
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2621189
Highly Enantioselective Reduction of α-Methylated Nitroalkenes
Burda, Edyta, Highly Enantioselective Reduction of α-Methylated Nitroalkenes. Angewandte Chemie (International ed. in English) 52 (35). , 2013
PUB | DOI | WoS | PubMed | Europe PMC
 
[160]
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2635953
Asymmetric Organocatalytic Aldol Reaction in Water: Mechanistic Insights and Development of a Semi-Continuously Operating Process
Rulli, Giuseppe, Asymmetric Organocatalytic Aldol Reaction in Water: Mechanistic Insights and Development of a Semi-Continuously Operating Process. Synthesis 45 (18). , 2013
PUB | DOI | WoS
 
[159]
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2637130
Towards catalyst compartimentation in combined chemo- and biocatalytic processes: Immobilization of alcohol dehydrogenases for the diastereoselective reduction of a β-hydroxy ketone obtained from an organocatalytic aldol reaction
Rulli, Giuseppe, Towards catalyst compartimentation in combined chemo- and biocatalytic processes: Immobilization of alcohol dehydrogenases for the diastereoselective reduction of a β-hydroxy ketone obtained from an organocatalytic aldol reaction. Journal of biotechnology 168 (3). , 2013
PUB | DOI | WoS | PubMed | Europe PMC
 
[158]
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2560792
Direct Oxidation of Cycloalkanes to Cycloalkanones with Oxygen in Water
Staudt, Svenja, Direct Oxidation of Cycloalkanes to Cycloalkanones with Oxygen in Water. Angewandte Chemie International Edition 52 (8). , 2013
PUB | DOI | WoS | PubMed | Europe PMC
 
[157]
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2612864
In Vitro Double Oxidation of n-Heptane with Direct Cofactor Regeneration
Mueller, Christina A., In Vitro Double Oxidation of n-Heptane with Direct Cofactor Regeneration. Advanced Synthesis & Catalysis 355 (9). , 2013
PUB | DOI | WoS
 
[156]
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2634611
Bio-integrated organic synthesis in industry: Biocatalytic breakthroughs, industrial processes, emerging fields
Gröger, Harald, Bio-integrated organic synthesis in industry: Biocatalytic breakthroughs, industrial processes, emerging fields. Journal of Biotechnology 168 (3). , 2013
PUB | DOI | WoS | PubMed | Europe PMC
 
[155]
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2647580
Development of a Continuously Operating Process for the Enantioselective Synthesis of a beta-Amino Acid Ester via a Solvent-Free Chemoenzymatic Reaction Sequence
Strompen, Simon, Development of a Continuously Operating Process for the Enantioselective Synthesis of a beta-Amino Acid Ester via a Solvent-Free Chemoenzymatic Reaction Sequence. Advanced Synthesis & Catalysis 355 (11-12). , 2013
PUB | DOI | WoS
 
[154]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2398888
Organocatalytic racemization of alpha-aryl propionates in the presence of water
Alfaro Blasco, M., Organocatalytic racemization of alpha-aryl propionates in the presence of water. Synth. Commun. 43 (1). , 2012
PUB | DOI | WoS
 
[153]
2012 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2398903
Asymmetric Biocatalytic Reduction of Ketones
Gröger, Harald, Asymmetric Biocatalytic Reduction of Ketones. Synthetic Methods VI – Enzymatic and Semi-Enzymatic 7 (). Oxford, 2012
PUB | DOI
 
[152]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2474296
Biocatalytic hydroxylation of n-butane with in situ cofactor regeneration at low temperature and under normal pressure
Staudt, Svenja, Biocatalytic hydroxylation of n-butane with in situ cofactor regeneration at low temperature and under normal pressure. Beilstein Journal of Organic Chemistry 8 (). , 2012
PUB | DOI | WoS | PubMed | Europe PMC
 
[151]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2445196
Combination of a Suzuki cross-coupling reaction using a water-soluble palladium catalyst with an asymmetric enzymatic reduction towards a one-pot reaction in aqueous medium at room temperature
Borchert, Sonja, Combination of a Suzuki cross-coupling reaction using a water-soluble palladium catalyst with an asymmetric enzymatic reduction towards a one-pot reaction in aqueous medium at room temperature. J. Mol. Catal. B: Enzym. 84 (SI). , 2012
PUB | DOI | WoS
 
[150]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2517832
Highly Enantioselective Organocatalytic Trifluoromethyl Carbinol Synthesis-A Caveat on Reaction Times and Product Isolation
Duangdee, Nongnaphat, Highly Enantioselective Organocatalytic Trifluoromethyl Carbinol Synthesis-A Caveat on Reaction Times and Product Isolation. Journal of the American Chemical Society 134 (27). , 2012
PUB | DOI | WoS | PubMed | Europe PMC
 
[149]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2553547
Efficient Enzymatic Amine Resolution at High Substrate Input Using Diethyl Malonate as an Acyl Donor of Low Hazard Potential
Simon, Sabine, Efficient Enzymatic Amine Resolution at High Substrate Input Using Diethyl Malonate as an Acyl Donor of Low Hazard Potential. Zeitschrift Fur Naturforschung Section B-A Journal Of Chemical Sciences 67b (10). , 2012
PUB | DOI | WoS
 
[148]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2474508
Large-Scale Synthesis of Singh's Catalyst in a One-Pot Procedure Starting from Proline
Berkessel, Albrecht, Large-Scale Synthesis of Singh's Catalyst in a One-Pot Procedure Starting from Proline. Organic Process Research & Development 16 (1). , 2012
PUB | DOI | WoS
 
[147]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2471821
Formal Asymmetric Hydration of Non-Activated Alkenes in Aqueous Medium through a "Chemoenzymatic Catalytic System"
Schnapperelle, Ingo, Formal Asymmetric Hydration of Non-Activated Alkenes in Aqueous Medium through a "Chemoenzymatic Catalytic System". Chemistry - A European Journal 18 (4). , 2012
PUB | DOI | WoS | PubMed | Europe PMC
 
[146]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2509926
Development of Biocatalytic Processes in Japan and Germany: From Research Synergies to Industrial Applications
Gröger, Harald, Development of Biocatalytic Processes in Japan and Germany: From Research Synergies to Industrial Applications. Chemistry - An Asian Journal 7 (6). , 2012
PUB | DOI | WoS | PubMed | Europe PMC
 
[145]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2445201
Kinetic investigation of a solvent-free, chemoenzymatic reaction sequence towards enantioselective synthesis of a ß-amino acid ester
Strompen, S., Kinetic investigation of a solvent-free, chemoenzymatic reaction sequence towards enantioselective synthesis of a ß-amino acid ester. Biotechnology and Bioengineering 109 (6). , 2012
PUB | DOI | WoS | PubMed | Europe PMC
 
[144]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2493243
Asymmetric addition of a nitrogen nucleophile to an enoate in the presence of a chiral phase-transfer catalyst: A novel approach toward enantiomerically enriched protected beta-amino acids
Weiss, Markus, Asymmetric addition of a nitrogen nucleophile to an enoate in the presence of a chiral phase-transfer catalyst: A novel approach toward enantiomerically enriched protected beta-amino acids. Heteroatom Chemistry 23 (2). , 2012
PUB | DOI | WoS
 
[143]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2490875
Synthesis of (S)-(+)-cericlamine through lipase-catalyzed aminolysis of azo acetates
Prechter, Agnes, Synthesis of (S)-(+)-cericlamine through lipase-catalyzed aminolysis of azo acetates. Organic & Biomolecular Chemistry 10 (17). , 2012
PUB | DOI | WoS | PubMed | Europe PMC
 
[142]
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344704
Combination of C=C Bond Formation by Wittig Reaction and Enzymatic C=C Bond Reduction in a One-Pot Process in Water
Krausser, Marina, Combination of C=C Bond Formation by Wittig Reaction and Enzymatic C=C Bond Reduction in a One-Pot Process in Water. CHEMCATCHEM 3 (2). , 2011
PUB | DOI | WoS
 
[141]
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344730
Asymmetric reduction of activated alkenes using an enoate reductase from Gluconobacter oxydans
Richter, Nina, Asymmetric reduction of activated alkenes using an enoate reductase from Gluconobacter oxydans. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY 89 (1). , 2011
PUB | DOI | WoS | PubMed | Europe PMC
 
[140]
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2398890
Combination of Olefin Metathesis and Enzymatic Ester Hydrolysis in Aqueous Media in a One-Pot Synthesis
Tenbrink, Katharina, Combination of Olefin Metathesis and Enzymatic Ester Hydrolysis in Aqueous Media in a One-Pot Synthesis. Adv. Synth. & Catal. 353 (13). , 2011
PUB | DOI | WoS
 
[139]
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2407538
Eisenkatalyse zur In-situ-Regenerierung oxidierter Cofaktoren durch Aktivierung und Reduktion von O2: ein synthetisches Metallporphyrin als biomimetische NAD(P)H-Oxidase
Maid, H., Eisenkatalyse zur In-situ-Regenerierung oxidierter Cofaktoren durch Aktivierung und Reduktion von O2: ein synthetisches Metallporphyrin als biomimetische NAD(P)H-Oxidase. Angew. Chem. 123 (10). , 2011
PUB | DOI | WoS | PubMed | Europe PMC
 
[138]
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2407610
Gesteuerte kinetisch oder thermodynamisch kontrollierte Organokatalyse und Anwendung in der chemoenzymatischen Synthese
Rulli, Giuseppe, Gesteuerte kinetisch oder thermodynamisch kontrollierte Organokatalyse und Anwendung in der chemoenzymatischen Synthese. Angew. Chem. 123 (34). , 2011
PUB | DOI
 
[137]
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344701
ChemCatChem: Cluster Issue on Chemoenzymatic Synthesis
Gröger, Harald, ChemCatChem: Cluster Issue on Chemoenzymatic Synthesis. CHEMCATCHEM 3 (2). , 2011
PUB | DOI | WoS
 
[136]
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344713
Direction of Kinetically versus Thermodynamically Controlled Organocatalysis and Its Application in Chemoenzymatic Synthesis
Rulli, Giuseppe, Direction of Kinetically versus Thermodynamically Controlled Organocatalysis and Its Application in Chemoenzymatic Synthesis. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 50 (34). , 2011
PUB | DOI | WoS | PubMed | Europe PMC
 
[135]
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344695
Chiral azo compounds: enantioselective synthesis and transformations into beta-amino alcohols and alpha-amino acids with a quaternary stereocenter
Dietz, Friedrich R., Chiral azo compounds: enantioselective synthesis and transformations into beta-amino alcohols and alpha-amino acids with a quaternary stereocenter. TETRAHEDRON LETTERS 52 (6). , 2011
PUB | DOI | WoS
 
[134]
2011 | Sammelwerksbeitrag | Im Druck | PUB-ID: 2397699
Reduction of Ketones and Aldehydes to Alcohols
Gröger, Harald, Reduction of Ketones and Aldehydes to Alcohols. Enzyme Catalysis in Organic Synthesis Chapter 12.1 (). Weinheim, 2011
PUB
 
[133]
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344721
Iron Catalysis for In Situ Regeneration of Oxidized Cofactors by Activation and Reduction of Molecular Oxygen: A Synthetic Metalloporphyrin as a Biomimetic NAD(P)H Oxidase
Maid, Harald, Iron Catalysis for In Situ Regeneration of Oxidized Cofactors by Activation and Reduction of Molecular Oxygen: A Synthetic Metalloporphyrin as a Biomimetic NAD(P)H Oxidase. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 50 (10). , 2011
PUB | DOI | WoS | PubMed | Europe PMC
 
[132]
2011 | Sammelwerksbeitrag | Im Druck | PUB-ID: 2397744
Hydrolysis and Formation of Carboxylic Acid Esters
Paravidino, M., Hydrolysis and Formation of Carboxylic Acid Esters. Enzyme Catalysis in Organic Synthesis Cahpter 8.1 (). Weinheim, 2011
PUB
 
[131]
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2394651
A study towards efficient L-threonine aldolase-catalyzed enantio- and diastereoselective aldol reactions of glycine with substituted benzaldehydes: biocatalyst production and process development
Baer, Katrin, A study towards efficient L-threonine aldolase-catalyzed enantio- and diastereoselective aldol reactions of glycine with substituted benzaldehydes: biocatalyst production and process development. Tetrahedron Asymmetry 22 (9). , 2011
PUB | DOI | WoS
 
[130]
2011 | Patent | PUB-ID: 2453495
Enzymreaktionen in Miniemulsionen
Gröger, Harald, Enzymreaktionen in Miniemulsionen. (). , 2011
PUB
 
[129]
2011 | Sammelwerksbeitrag | Im Druck | PUB-ID: 2397781
Reductive Amination of alpha-Keto Acids
Hummel, W., Reductive Amination of alpha-Keto Acids. Enzyme Catalysis in Organic Synthesis Chapter 12.3 (). Weinheim, 2011
PUB
 
[128]
2011 | Patent | Veröffentlicht | PUB-ID: 2458477
Verfahren zur Herstellung von enantiomerenangereicherten Azoverbindungen, Aminoalkoholen und Aminosäuren mit einem quartären Kohlenstoffzentrum
Heinrich, M., Verfahren zur Herstellung von enantiomerenangereicherten Azoverbindungen, Aminoalkoholen und Aminosäuren mit einem quartären Kohlenstoffzentrum. (). , 2011
PUB
 
[127]
2011 | Zeitschriftenaufsatz | Im Druck | PUB-ID: 2445179
Formal Enantioselective Hydratation of Alkenes: Combination of Wacker-Oxidation and Biocatalytic Reduction in a One-Pot Process in Aqueous Media
Schnapperelle, I., Formal Enantioselective Hydratation of Alkenes: Combination of Wacker-Oxidation and Biocatalytic Reduction in a One-Pot Process in Aqueous Media. Chem. Eur. J. (). , 2011
PUB
 
[126]
2011 | Sammelwerksbeitrag | Im Druck | PUB-ID: 2445173
Introduction - Milestones of the Development of Enzyme Catalysis in Organic Synthesis
Gröger, Harald, Introduction - Milestones of the Development of Enzyme Catalysis in Organic Synthesis. Enzyme Catalysis in Organic Synthesis (). Weinheim, 2011
PUB
 
[125]
2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344754
Enantioselective biocatalytic synthesis of (S)-monastrol
Alfaro Blasco, Maria, Enantioselective biocatalytic synthesis of (S)-monastrol. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS 20 (15). , 2010
PUB | DOI | WoS | PubMed | Europe PMC
 
[124]
2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344761
Expanding the Application Range of Aldolases: Novel Asymmetric Syntheses of alpha-Methylated beta-Hydroxy alpha-Amino Acids and beta-Amino Alcohols
Baer, Katrin, Expanding the Application Range of Aldolases: Novel Asymmetric Syntheses of alpha-Methylated beta-Hydroxy alpha-Amino Acids and beta-Amino Alcohols. CHEMCATCHEM 2 (8). , 2010
PUB | DOI | WoS
 
[123]
2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344778
Enantio- and Diastereoselective Chemoenzymatic Synthesis of C2-Symmetric Biaryl-Containing Diols
Burda, Edyta, Enantio- and Diastereoselective Chemoenzymatic Synthesis of C2-Symmetric Biaryl-Containing Diols. CHEMCATCHEM 2 (1). , 2010
PUB | DOI | WoS
 
[122]
2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344737
Threonine aldolases-screening, properties and applications in the synthesis of non-proteinogenic beta-hydroxy-alpha-amino acids
Dückers, Nina, Threonine aldolases-screening, properties and applications in the synthesis of non-proteinogenic beta-hydroxy-alpha-amino acids. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY 88 (2). , 2010
PUB | DOI | WoS | PubMed | Europe PMC
 
[121]
2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344744
Highly conserved progesterone 5 beta-reductase genes (P5 beta R) from 5 beta-cardenolide-free and 5 beta-cardenolide-producing angiosperms
Bauer, Peter, Highly conserved progesterone 5 beta-reductase genes (P5 beta R) from 5 beta-cardenolide-free and 5 beta-cardenolide-producing angiosperms. PHYTOCHEMISTRY 71 (13). , 2010
PUB | DOI | WoS | PubMed | Europe PMC
 
[120]
2010 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2344784
Regeneration of Nicotinamide Coenzymes: Principles and Applications for the Synthesis of Chiral Compounds
Weckbecker, Andrea, Regeneration of Nicotinamide Coenzymes: Principles and Applications for the Synthesis of Chiral Compounds. BIOSYSTEMS ENGINEERING I: CREATING SUPERIOR BIOCATALYSTS 120 (). , 2010
PUB | DOI | WoS | PubMed | Europe PMC
 
[119]
2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344772
Enantioselective Biocatalytic Reduction of Non-protected Hydroxyacetophenones
Neupert, Adrian, Enantioselective Biocatalytic Reduction of Non-protected Hydroxyacetophenones. Zeitschrift für Naturforschung. Section B, a journal of chemical sciences 65 (3). , 2010
PUB | DOI | WoS
 
[118]
2010 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2396569
Enzyme-Catalyzed Asymmetric Synthesis
Gröger, Harald, Enzyme-Catalyzed Asymmetric Synthesis. Catalytic Asymmetric Synthesis 6 (). Hoboken, New Jersey, 2010
PUB
 
[117]
2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344790
Towards a greener synthesis of (S)-3-aminobutanoic acid: process development and environmental assessment
Weiss, Markus, Towards a greener synthesis of (S)-3-aminobutanoic acid: process development and environmental assessment. GREEN CHEMISTRY 12 (9). , 2010
PUB | DOI | WoS
 
[116]
2010 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2396563
Enzyme-Catalyzed Asymmetric Reduction of Ketones
Gröger, Harald, Enzyme-Catalyzed Asymmetric Reduction of Ketones. Encyclopedia of Industrial Biotechnology, Bioprocess, Bioseparation, and Cell Technology 3 (). New York, 2010
PUB
 
[115]
2010 | Patent | PUB-ID: 2453130
Verfahren zur Herstellung von optisch aktiven Aminosäuren mittels eines Ganzzellkatalysators
Altenbuchner, J., Verfahren zur Herstellung von optisch aktiven Aminosäuren mittels eines Ganzzellkatalysators. (). , 2010
PUB
 
[114]
2010 | Patent | PUB-ID: 2453301
Verfahren zur enzymatischen Umsetzung von Alkanen
Gröger, Harald, Verfahren zur enzymatischen Umsetzung von Alkanen. (). , 2010
PUB
 
[113]
2010 | Patent | Veröffentlicht | PUB-ID: 2399883
Verfahren zur Herstellung von überwiegend ein Enantiomer enthaltendem 1,1,1-Trifluorpropanol
Doderer, K., Verfahren zur Herstellung von überwiegend ein Enantiomer enthaltendem 1,1,1-Trifluorpropanol. (). , 2010
PUB
 
[112]
2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344767
Purification, cloning, and overexpression of an alcohol dehydrogenase from Nocardia globerula reducing aliphatic ketones and bulky ketoesters
Parkot, Julia, Purification, cloning, and overexpression of an alcohol dehydrogenase from Nocardia globerula reducing aliphatic ketones and bulky ketoesters. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY 86 (6). , 2010
PUB | DOI | WoS | PubMed | Europe PMC
 
[111]
2010 | Patent | PUB-ID: 2453169
Herstellung optisch aktiver Alkohole mit Hilfe von Ganzzellkatalsatoren
Gröger, Harald, Herstellung optisch aktiver Alkohole mit Hilfe von Ganzzellkatalsatoren. (). , 2010
PUB
 
[110]
2009 | Patent | PUB-ID: 2453000
ADH aus Rhodococcus erythropolis
Hummel, W., ADH aus Rhodococcus erythropolis. (). , 2009
PUB
 
[109]
2009 | Patent | PUB-ID: 2453012
Verfahren zur enzymatischen Herstellung enantiomerenangereicherter ß-Aminosäuren
Gröger, Harald, Verfahren zur enzymatischen Herstellung enantiomerenangereicherter ß-Aminosäuren. (). , 2009
PUB
 
[108]
2009 | Patent | PUB-ID: 2453151
Neue Alkoholdehydrogenasen
Schulze, R., Neue Alkoholdehydrogenasen. (). , 2009
PUB
 
[107]
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344799
Recombinant Delta(4,5)-Steroid 5 beta-Reductases as Biocatalysts for the Reduction of Activated C=C-Double Bonds in Monocyclic and Acyclic Molecules
Burda, Edyta, Recombinant Delta(4,5)-Steroid 5 beta-Reductases as Biocatalysts for the Reduction of Activated C=C-Double Bonds in Monocyclic and Acyclic Molecules. ADVANCED SYNTHESIS & CATALYSIS 351 (17). , 2009
PUB | DOI | WoS
 
[106]
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344823
Sequential and Modular Synthesis of Chiral 1,3-Diols with Two Stereogenic Centers: Access to All Four Stereoisomers by Combination of Organo- and Biocatalysis
Baer, Katrin, Sequential and Modular Synthesis of Chiral 1,3-Diols with Two Stereogenic Centers: Access to All Four Stereoisomers by Combination of Organo- and Biocatalysis. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 48 (49). , 2009
PUB | DOI | WoS | PubMed | Europe PMC
 
[105]
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2346641
Multistep one-pot processes in aqueous media by combination of palladium-catalyzed cross-coupling reactions and biotransformations
Burda, Edyta, Multistep one-pot processes in aqueous media by combination of palladium-catalyzed cross-coupling reactions and biotransformations. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY 238 (). , 2009
PUB | WoS
 
[104]
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344795
Asymmetric Synthesis of All Stereoisomers of alpha-Methylthreonine Using an Organocatalytic Steglich Rearrangement Reaction as a Key Step
Dietz, Friedrich R., Asymmetric Synthesis of All Stereoisomers of alpha-Methylthreonine Using an Organocatalytic Steglich Rearrangement Reaction as a Key Step. SYNTHESIS-STUTTGART (24). , 2009
PUB | DOI | WoS
 
[103]
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2346645
Practical, Highly Enantioselective Chemoenzymatic One-Pot Synthesis of Short-Chain Aliphatic beta-Amino Acid Esters
Weiss, Markus, Practical, Highly Enantioselective Chemoenzymatic One-Pot Synthesis of Short-Chain Aliphatic beta-Amino Acid Esters. SYNLETT 2009 (08). , 2009
PUB | DOI | WoS
 
[102]
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2407531
Sequenzielle und modulare Synthese von chiralen 1,3-Diolen mit zwei Stereozentren: Zugang zu allen vier Stereoisomeren durch Kombination von Organo- und Biokatalyse
Baer, K., Sequenzielle und modulare Synthese von chiralen 1,3-Diolen mit zwei Stereozentren: Zugang zu allen vier Stereoisomeren durch Kombination von Organo- und Biokatalyse. Angew. Chem. 121 (49). , 2009
PUB | DOI
 
[101]
2009 | Patent | PUB-ID: 2453286
Verfahren zur Herstellung von enantimerenangereicherten Aminen
Doderer, K., Verfahren zur Herstellung von enantimerenangereicherten Aminen. (). , 2009
PUB
 
[100]
2009 | Patent | Veröffentlicht | PUB-ID: 2400139
Aufarbeitung von Reaktionslösungen aus Ganzzell-Biotransformationen
Gröger, Harald, Aufarbeitung von Reaktionslösungen aus Ganzzell-Biotransformationen. (). , 2009
PUB
 
[99]
2009 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2396636
Biocatalytic Synthesis of Natural and Non-Natural alpha-Amino Acids
Gröger, Harald, Biocatalytic Synthesis of Natural and Non-Natural alpha-Amino Acids. Wiley Encyclopedia of Chemical Biology 1 (). Hoboken, 2009
PUB
 
[98]
2009 | Patent | PUB-ID: 2453051
Gekoppeltes cofaktorabhängiges enzymatisches Reaktionssystem
Gröger, Harald, Gekoppeltes cofaktorabhängiges enzymatisches Reaktionssystem. (). , 2009
PUB
 
[97]
2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344831
Novel catalytic synthetic route to protected alpha-methyl threonine and the first asymmetric acetyl migration in a Steglich rearrangement reaction
Dietz, Friedrich R., Novel catalytic synthetic route to protected alpha-methyl threonine and the first asymmetric acetyl migration in a Steglich rearrangement reaction. SYNLETT 2008 (5). , 2008
PUB | DOI | WoS
 
[96]
2008 | Konferenzbeitrag | Veröffentlicht | PUB-ID: 2347145
Asymmetric organocatalysis on a technical scale: current status and future challenges
Gröger, Harald, Asymmetric organocatalysis on a technical scale: current status and future challenges. Organocatalysis (). Berlin u.a., 2008
PUB | DOI | PubMed | Europe PMC
 
[95]
2008 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2396697
Asymmetric Organocatalysis on a Technical Scale: Current Status and Future Challenges
Gröger, Harald, Asymmetric Organocatalysis on a Technical Scale: Current Status and Future Challenges. Ernst Schering Foundation Symposium Proceedings 2007-2: Organocatalysis (). Berlin, Heidelberg, 2008
PUB | DOI
 
[94]
2008 | Patent | PUB-ID: 2453245
Verfahren zur Herstellung von enantiomerenangereicherten Alkylencarbonaten
Gröger, Harald, Verfahren zur Herstellung von enantiomerenangereicherten Alkylencarbonaten. (). , 2008
PUB
 
[93]
2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344840
Enantioselective C-C bond ligation using recombinant Escherichia coli-whole-cell biocatalysts
Dominguez de Maria, Pablo, Enantioselective C-C bond ligation using recombinant Escherichia coli-whole-cell biocatalysts. ADVANCED SYNTHESIS & CATALYSIS 350 (1). , 2008
PUB | DOI | WoS
 
[92]
2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344835
Modular Chemoenzymatic One-Pot Syntheses in Aqueous Media: Combination of a Palladium-Catalyzed Cross-Coupling with an Asymmetric Biotransformation
Burda, Edyta, Modular Chemoenzymatic One-Pot Syntheses in Aqueous Media: Combination of a Palladium-Catalyzed Cross-Coupling with an Asymmetric Biotransformation. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 47 (49). , 2008
PUB | DOI | WoS | PubMed | Europe PMC
 
[91]
2008 | Patent | PUB-ID: 2453216
Verfahren zur Herstellung von enantiomerenangereicherten Aminen und Amiden durch enzymatische Racematspaltung
Gröger, Harald, Verfahren zur Herstellung von enantiomerenangereicherten Aminen und Amiden durch enzymatische Racematspaltung. (). , 2008
PUB
 
[90]
2008 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2396674
Chiral Trivalent Phosphorus Compounds as Organocatalysts in Asymmetric Synthesis
Gröger, Harald, Chiral Trivalent Phosphorus Compounds as Organocatalysts in Asymmetric Synthesis. Phosphorous Ligands in Asymmetric Catalysis - Synthesis and Applications 3 (). Weinheim, 2008
PUB
 
[89]
2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2407518
Modulare chemoenzymatische Eintopfsynthesen im wässrigen Medium: Kombination einer Palladium-katalysierten Kreuzkupplung mit einer asymmetrischen Biotransformation
Burda, E., Modulare chemoenzymatische Eintopfsynthesen im wässrigen Medium: Kombination einer Palladium-katalysierten Kreuzkupplung mit einer asymmetrischen Biotransformation. Angew. Chem. 120 (49). , 2008
PUB | DOI
 
[88]
2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2346666
Practical two-step synthesis of an enantiopure aliphatic terminal (S)-epoxide based on reduction of haloalkanones with ``Designer Cells''
Berkessel, Albrecht, Practical two-step synthesis of an enantiopure aliphatic terminal (S)-epoxide based on reduction of haloalkanones with ``Designer Cells''. ADVANCED SYNTHESIS & CATALYSIS 349 (17-18). , 2007
PUB | DOI | WoS
 
[87]
2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2346685
Enantioselective reduction of 4-fluoroacetophenone at high substrate concentration using a tailor-made recombinant whole-cell catalyst
Gröger, Harald, Enantioselective reduction of 4-fluoroacetophenone at high substrate concentration using a tailor-made recombinant whole-cell catalyst. ADVANCED SYNTHESIS & CATALYSIS 349 (4-5). , 2007
PUB | DOI | WoS
 
[86]
2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344854
Alcohol dehydrogenase whole-cell catalysts - A broad technology platform for life science applications
Osswald, S., Alcohol dehydrogenase whole-cell catalysts - A broad technology platform for life science applications. CHIMICA OGGI-CHEMISTRY TODAY 25 (5, S). , 2007
PUB
 
[85]
2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344865
Asymmetric synthesis of aliphatic 2-hydroxy ketones by enzymatic carboligation of aldehydes
Dominguez de Maria, Pablo, Asymmetric synthesis of aliphatic 2-hydroxy ketones by enzymatic carboligation of aldehydes. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY 2007 (18). , 2007
PUB | DOI | WoS
 
[84]
2007 | Patent | PUB-ID: 2453180
Verfahren zur Herstellung primärer Alkohole
Gröger, Harald, Verfahren zur Herstellung primärer Alkohole. (). , 2007
PUB
 
[83]
2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2346674
Enantioselective one-pot two-step synthesis of hydrophobic allylic alcohols in aqueous medium through the combination of a wittig reaction and an enzymatic ketone reduction
Krausser, Marina, Enantioselective one-pot two-step synthesis of hydrophobic allylic alcohols in aqueous medium through the combination of a wittig reaction and an enzymatic ketone reduction. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY 2007 (31). , 2007
PUB | DOI | WoS
 
[82]
2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2346679
Biocatalytic alclehyde reduction using tailor-made whole-cell catalysts: a novel synthesis of the aroma chemical cinnamyl alcohol
Chamouleau, Francoise, Biocatalytic alclehyde reduction using tailor-made whole-cell catalysts: a novel synthesis of the aroma chemical cinnamyl alcohol. FLAVOUR AND FRAGRANCE JOURNAL 22 (3). , 2007
PUB | DOI | WoS
 
[81]
2007 | Patent | PUB-ID: 2399880
Alkoholdehydrogenase aus Nocardia globulera und deren Verwendung
Hummel, W., Alkoholdehydrogenase aus Nocardia globulera und deren Verwendung. (). , 2007
PUB
 
[80]
2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2396781
Enantioselektive Enzymreaktionen in Miniemulsionen als effiziente "Nanoreaktoren"
Gröger, Harald, Enantioselektive Enzymreaktionen in Miniemulsionen als effiziente "Nanoreaktoren". Angew. Chem. Int. Ed. (45). , 2006
PUB
 
[79]
2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2407494
Enantioselektive Ketonreduktion mit "Designerzellen" bei hohen Substratkonzentrationen: Hocheffizienter Zugang zu funktionalisierten optisch aktiven Alkoholen
Gröger, Harald, Enantioselektive Ketonreduktion mit "Designerzellen" bei hohen Substratkonzentrationen: Hocheffizienter Zugang zu funktionalisierten optisch aktiven Alkoholen. Angew. Chem. 118 (34). , 2006
PUB | DOI
 
[78]
2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347147
Enantioselective reduction of ketones with "designer cells" at high substrate concentrations: highly efficient access to functionalized optically active alcohols
Gröger, Harald, Enantioselective reduction of ketones with "designer cells" at high substrate concentrations: highly efficient access to functionalized optically active alcohols. Angewandte Chemie International Edition 45 (34). , 2006
PUB | DOI | WoS | PubMed | Europe PMC
 
[77]
2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2396830
Preparative Enantioselective Synthesis of Benzoins and (R)-2-Hydroxy-1-phenyl-propanone Using Benzaldehyde Lyase
Dominguez de Maria, P., Preparative Enantioselective Synthesis of Benzoins and (R)-2-Hydroxy-1-phenyl-propanone Using Benzaldehyde Lyase. J. Mol. Catal. B: Enzym. 38 (1). , 2006
PUB | DOI | WoS
 
[76]
2006 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2396733
Biocatalytic Concepts for the Synthesis of Optically Active Amines
Buchholz, S., Biocatalytic Concepts for the Synthesis of Optically Active Amines. Biocatalysis in the Pharmaceutical and Biotechnology Industries (). New York, 2006
PUB
 
[75]
2006 | Patent | PUB-ID: 2399875
Verfahren zur Herstellung von enantiomer angereicherten alpha-Hydroxyketonen
Dominguez de Maria, P., Verfahren zur Herstellung von enantiomer angereicherten alpha-Hydroxyketonen. (). , 2006
PUB
 
[74]
2006 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2396749
Enationselective Biocatalytic Reduction of Ketones for the Synthesis of Optically Active Alcohols
Buchholz, S., Enationselective Biocatalytic Reduction of Ketones for the Synthesis of Optically Active Alcohols. Biocatalysis in the Pharmaceutical and Biotechnology Industries Chapter 32 (). New York, 2006
PUB
 
[73]
2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2396819
A "Second Generation-Process" for the Synthesis of L-Neopentylglycine: Asymmetric Reductive Amination Using a Recombinant Whole Cell Catalyst
Gröger, Harald, A "Second Generation-Process" for the Synthesis of L-Neopentylglycine: Asymmetric Reductive Amination Using a Recombinant Whole Cell Catalyst. Org. Proc. Res. Developm. 10 (3). , 2006
PUB | DOI | WoS
 
[72]
2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2407476
Enantioselektive Enzymreaktionen in Miniemulsionen als effiziente "Nanoreaktoren"
Gröger, Harald, Enantioselektive Enzymreaktionen in Miniemulsionen als effiziente "Nanoreaktoren". Angew. Chem. (118). , 2006
PUB
 
[71]
2005 | Patent | PUB-ID: 2399843
Enzymatische Reaktionen in Gegenwart ionischer Additive
Wallert, S., Enzymatische Reaktionen in Gegenwart ionischer Additive. (). , 2005
PUB
 
[70]
2005 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2396902
Ganzzellbiokatalyse
Buchholz, S., Ganzzellbiokatalyse. Angewandte Mikrobiologie Chapter 8 (). Heidelberg, 2005
PUB
 
[69]
2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2396930
Improved Process for the Enantioselective Hydrolysis of Prochiral Diethyl Malonates Catalyzed by Pig Liver Esterase
Dominguez de Maria, P., Improved Process for the Enantioselective Hydrolysis of Prochiral Diethyl Malonates Catalyzed by Pig Liver Esterase. Synlett (11). , 2005
PUB | DOI | WoS
 
[68]
2005 | Monographie | Veröffentlicht | PUB-ID: 2397104
Asymmetric Organocatalysis
Berkessel, A., Asymmetric Organocatalysis. (). Weinheim, 2005
PUB | DOI
 
[67]
2005 | Patent | PUB-ID: 2399762
Verfahren zur Herstellung von D-Aminosäuren
Hummel, H., Verfahren zur Herstellung von D-Aminosäuren. (). , 2005
PUB
 
[66]
2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2396908
Ionic liquids as Additives in the Pig Liver Esterase (PLE) Catalyzed Synthesis of Chiral Disubstituted Malonates
Wallert, S., Ionic liquids as Additives in the Pig Liver Esterase (PLE) Catalyzed Synthesis of Chiral Disubstituted Malonates. Green Chem. 7 (8). , 2005
PUB | DOI | WoS
 
[65]
2004 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347164
The first aminoacylase-catalyzed enantioselective synthesis of aromatic beta-amino acids
Gröger, Harald, The first aminoacylase-catalyzed enantioselective synthesis of aromatic beta-amino acids. Org. Biomol. Chemistry 2 (14). , 2004
PUB | DOI | WoS | PubMed | Europe PMC
 
[64]
2004 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397106
From Enzymes to "Designer Bugs" in Reductive Amination: A New Process for the Synthesis of L-tert-Leucine Using a Whole Cell-Catalyst
Menzel, A., From Enzymes to "Designer Bugs" in Reductive Amination: A New Process for the Synthesis of L-tert-Leucine Using a Whole Cell-Catalyst. Eng. Life Sciences 4 (). , 2004
PUB
 
[63]
2004 | Patent | PUB-ID: 2399668
Gekoppeltes enzymatisches Reaktionssystem
Gröger, Harald, Gekoppeltes enzymatisches Reaktionssystem. (). , 2004
PUB
 
[62]
2004 | Patent | PUB-ID: 2399670
Gekoppeltes enzymatisches Reaktionssystem unter Einsatz einer Formiatdehydrogenase aus Candida boidinii
Gröger, Harald, Gekoppeltes enzymatisches Reaktionssystem unter Einsatz einer Formiatdehydrogenase aus Candida boidinii. (). , 2004
PUB
 
[61]
2004 | Patent | PUB-ID: 2399682
Enzymatisches Reaktionssystem
Hummel, W., Enzymatisches Reaktionssystem. (). , 2004
PUB
 
[60]
2004 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397117
Preparative Asymmetric Reduction of Ketones in a Biphasic Medium with an (S)-AIcohol Dehydrogenase under in situ-Cofactor-Recycling with a Formate Dehydrogenase
Gröger, Harald, Preparative Asymmetric Reduction of Ketones in a Biphasic Medium with an (S)-AIcohol Dehydrogenase under in situ-Cofactor-Recycling with a Formate Dehydrogenase. Tetrahedron 60 (3). , 2004
PUB | DOI | WoS
 
[59]
2004 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2397155
Nitroaldol Reaction
Shibasaki, M., Nitroaldol Reaction. Comprehensive Asymmetric Catalysis, Supplement 1 (). Heidelberg, 2004
PUB
 
[58]
2004 | Patent | PUB-ID: 2399679
Verwendung von Malatdehydrogenase zur NADH-Regenerierung
Naamniek, S., Verwendung von Malatdehydrogenase zur NADH-Regenerierung. (). , 2004
PUB
 
[57]
2004 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397147
Enzymatic Cofactor-Regeneration Technology Platforms for Chiral alpha-Amino Acids and Alcohols
May, O., Enzymatic Cofactor-Regeneration Technology Platforms for Chiral alpha-Amino Acids and Alcohols. Speciality Chemicals Magazine 5 (). , 2004
PUB
 
[56]
2004 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2397178
Methods for the Biocatalytic Production of L-Amino Acids on Industrial Scale
Gröger, Harald, Methods for the Biocatalytic Production of L-Amino Acids on Industrial Scale. Large-Scale Asymmetric Catalysis (). Weinheim, 2004
PUB
 
[55]
2004 | Patent | PUB-ID: 2399703
Gekoppeltes cofaktorabhängiges enzymatisches Reaktionssystem
Rollmann, C., Gekoppeltes cofaktorabhängiges enzymatisches Reaktionssystem. (). , 2004
PUB
 
[54]
2003 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347176
Practical asymmetric enzymatic reduction through discovery of a dehydrogenase-compatible biphasic reaction media
Gröger, Harald, Practical asymmetric enzymatic reduction through discovery of a dehydrogenase-compatible biphasic reaction media. Organic Letters 5 (2). , 2003
PUB | DOI | WoS | PubMed | Europe PMC
 
[53]
2003 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347173
Catalytic enantioselective Strecker reactions and analogous syntheses
Gröger, Harald, Catalytic enantioselective Strecker reactions and analogous syntheses. Chemical Reviews 103 (8). , 2003
PUB | DOI | WoS | PubMed | Europe PMC
 
[52]
2003 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397219
Towards a Large-Scale Asymmetric Reduction Process with Isolated Enzymes: Expression of an (S)-Alcohol Dehydrogenase in E. coli and Studies on the Synthetic Potential of this Biocatalyst
Hummel, W., Towards a Large-Scale Asymmetric Reduction Process with Isolated Enzymes: Expression of an (S)-Alcohol Dehydrogenase in E. coli and Studies on the Synthetic Potential of this Biocatalyst. Adv. Synth. Catal. 345 (). , 2003
PUB
 
[51]
2003 | Patent | PUB-ID: 2399663
Verfahren zur enzymatischen Herstellung enantiomerenangereicherter ß-Aminosäuren
Gröger, Harald, Verfahren zur enzymatischen Herstellung enantiomerenangereicherter ß-Aminosäuren. (). , 2003
PUB
 
[50]
2003 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2397232
Simple Amino acids and Short-chain Peptides as Efficient Metal-free Catalysts in Asymmetric Synthesis
Gröger, Harald, Simple Amino acids and Short-chain Peptides as Efficient Metal-free Catalysts in Asymmetric Synthesis. Organic Synthesis Highlights (). Weinheim, 2003
PUB
 
[49]
2003 | Patent | PUB-ID: 2399205
Verfahren zur Kristallisation von Oxonorleucinacetal
Schwarm, M., Verfahren zur Kristallisation von Oxonorleucinacetal. (). , 2003
PUB
 
[48]
2003 | Patent | PUB-ID: 2399215
Verfahren zur Herstellung von optisch aktiven ß-Aminocarbonsäuren aus racemischen N-acetylierten ß-Aminocarbonsäuren
Gröger, Harald, Verfahren zur Herstellung von optisch aktiven ß-Aminocarbonsäuren aus racemischen N-acetylierten ß-Aminocarbonsäuren. (). , 2003
PUB
 
[47]
2002 | Patent | PUB-ID: 2399141
Verfahren zur Herstellung von Amiden
Sans, J., Verfahren zur Herstellung von Amiden. (). , 2002
PUB
 
[46]
2002 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397245
Biocatalytic Asymmetric Hydrocyanation in the Presence of (R)-Oxynitrilases Entrapped in Lens-Shaped Gels
Gröger, Harald, Biocatalytic Asymmetric Hydrocyanation in the Presence of (R)-Oxynitrilases Entrapped in Lens-Shaped Gels. Landbauforschung Völkenrode Sonderheft (Special Issue) 241 (). , 2002
PUB
 
[45]
2002 | Patent | PUB-ID: 2399100
Verfahren zur Herstellung von N-Phosphonomethyliminodiessigsäure
Gröger, Harald, Verfahren zur Herstellung von N-Phosphonomethyliminodiessigsäure. (). , 2002
PUB
 
[44]
2002 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2397254
Special Catalysts and Processes: Biocatalysis and Enzyme-Analogous Processes
Schultz, C., Special Catalysts and Processes: Biocatalysis and Enzyme-Analogous Processes. Applied Homogeneous Catalysis with Organometallic Compounds 2 (). Weinheim, 2002
PUB
 
[43]
2002 | Patent | PUB-ID: 2399176
Verfahren zur Herstellung von optisch aktiven Cyanhydrinen
Shibasaki, M., Verfahren zur Herstellung von optisch aktiven Cyanhydrinen. (). , 2002
PUB
 
[42]
2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397265
The Development of New Monometallic Bifunctional Catalysts with Lewis Acid and Lewis Base properties, and their Applicationin Asymmetric Cyanation Reactions
Gröger, Harald, The Development of New Monometallic Bifunctional Catalysts with Lewis Acid and Lewis Base properties, and their Applicationin Asymmetric Cyanation Reactions. Chem. Eur. J. 7 (). , 2001
PUB
 
[41]
2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347186
The development of new monometallic bifunctional catalysts with Lewis acid and Lewis base properties, and their application in asymmetric cyanation reactions
Gröger, Harald, The development of new monometallic bifunctional catalysts with Lewis acid and Lewis base properties, and their application in asymmetric cyanation reactions. Chemistry 7 (24). , 2001
PUB | DOI | PubMed | Europe PMC
 
[40]
2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397268
Enzymatic Routes to Enantiomerically Pure Aromatic alpha-Hydroxy Carboxylic Acids: A Further Example for the Diversity of Biocatalysis
Gröger, Harald, Enzymatic Routes to Enantiomerically Pure Aromatic alpha-Hydroxy Carboxylic Acids: A Further Example for the Diversity of Biocatalysis. Adv. Synth. Catal. 343 (). , 2001
PUB
 
[39]
2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397279
The Application of L-Proline as an Enzyme Mimic and Further New Asymmetric Syntheses Using Small Organic Molecules as Chiral Catalysis
Gröger, Harald, The Application of L-Proline as an Enzyme Mimic and Further New Asymmetric Syntheses Using Small Organic Molecules as Chiral Catalysis. Angew. Chem. Int. Ed. 40 (). , 2001
PUB
 
[38]
2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347191
Asymmetric synthesis of an (R)-cyanohydrin using enzymes entrapped in lens-shaped gels
Gröger, Harald, Asymmetric synthesis of an (R)-cyanohydrin using enzymes entrapped in lens-shaped gels. Organic Letters 3 (13). , 2001
PUB | DOI | WoS | PubMed | Europe PMC
 
[37]
2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397285
Anti- and Syn-Selective Cyanosilylation Reactions Promoted by a Sugar-Based Bifunctional Catalyst: Stereoselective Synthesis of Essential building Blocks for HIV Protease Inhibitors and Bestatin
Manickam, G., Anti- and Syn-Selective Cyanosilylation Reactions Promoted by a Sugar-Based Bifunctional Catalyst: Stereoselective Synthesis of Essential building Blocks for HIV Protease Inhibitors and Bestatin. Synlett (). , 2001
PUB
 
[36]
2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2407474
Die Anwendung von L-Prolin als Enzymmimetikum und weitere neue asymmetrische Synthesen mit kleinen organischen Molekülen als chiralen Katalysatoren
Gröger, Harald, Die Anwendung von L-Prolin als Enzymmimetikum und weitere neue asymmetrische Synthesen mit kleinen organischen Molekülen als chiralen Katalysatoren. Angewandte Chem. (113). , 2001
PUB
 
[35]
2001 | Patent | PUB-ID: 2399121
Method for Producing Optically Active Cyanohydrins
Gröger, Harald, Method for Producing Optically Active Cyanohydrins. (). , 2001
PUB
 
[34]
2001 | Patent | PUB-ID: 2399126
Verfahren zur Herstellung von Amiden oder Estern
Gröger, Harald, Verfahren zur Herstellung von Amiden oder Estern. (). , 2001
PUB
 
[33]
2000 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347215
Catalytic concepts for the enantioselective synthesis of alpha-amino and alpha-hydroxy phosphonates
Gröger, Harald, Catalytic concepts for the enantioselective synthesis of alpha-amino and alpha-hydroxy phosphonates. Chemistry 6 (6). , 2000
PUB | DOI | PubMed | Europe PMC
 
[32]
2000 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397396
The First Synthesis of a 2H-1,4-Benzothiazine-based Phosphine Oxide and Sulfide
Gröger, Harald, The First Synthesis of a 2H-1,4-Benzothiazine-based Phosphine Oxide and Sulfide. Phosphorus, Sulfur, Silicon 166 (). , 2000
PUB
 
[31]
2000 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397409
Preparation of an Enantiomerically Pure Helical Nickel(II) Complex Using a New Chiral Tetradentate Ligand Derived from an Industrial Waste Material
Pennemann, H., Preparation of an Enantiomerically Pure Helical Nickel(II) Complex Using a New Chiral Tetradentate Ligand Derived from an Industrial Waste Material. J. Chem. Soc. Dalton Trans. (). , 2000
PUB
 
[30]
2000 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397430
1,3,5-Triazines, versatile industrial building blocks: Synthetic approaches and applications
Gröger, Harald, 1,3,5-Triazines, versatile industrial building blocks: Synthetic approaches and applications. Chimica Oggi/Chemistry Today 18 (3/4) (). , 2000
PUB
 
[29]
2000 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397352
Concept of Improved Rigidity: How to Make Enantioselective Hydrophosphonylation of Cyclic Imines Catalyzed by Chiral Heterobimetallic Lanthanoid Complexes Almost Perfect
Schlemminger, I., Concept of Improved Rigidity: How to Make Enantioselective Hydrophosphonylation of Cyclic Imines Catalyzed by Chiral Heterobimetallic Lanthanoid Complexes Almost Perfect. J. Org. Chem. 65 (). , 2000
PUB
 
[28]
2000 | Patent | PUB-ID: 2399023
Precursors for PNA-Monomers
Martens, J., Precursors for PNA-Monomers. (). , 2000
PUB
 
[27]
2000 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397440
Moderne Methoden der Suzuki-Kreuzkupplung: Die langerwarteten universellen Synthesevarianten mit Arylchloriden
Gröger, Harald, Moderne Methoden der Suzuki-Kreuzkupplung: Die langerwarteten universellen Synthesevarianten mit Arylchloriden. J. Prakt. Chem. 342 (). , 2000
PUB
 
[26]
2000 | Patent | PUB-ID: 2399111
Verfahren zur Herstellung von N-Phosphonomethyliminodiessigsäure
Gröger, Harald, Verfahren zur Herstellung von N-Phosphonomethyliminodiessigsäure. (). , 2000
PUB
 
[25]
1999 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2347897
The Asymmetric Nitroaldol Reaction: Addition of Nitroalkanes to Aldehydes in the Presence of Heterobimetallic Lanthanoid Catalysts
Shibasaki, M., The Asymmetric Nitroaldol Reaction: Addition of Nitroalkanes to Aldehydes in the Presence of Heterobimetallic Lanthanoid Catalysts. Comprehensive Asymmetric Catalysis, Vol 3 (). Heidelberg, 1999
PUB
 
[24]
1999 | Zeitschriftenaufsatz | PUB-ID: 2347912
The First Catalytic Asymmetric Nitro-Mannich-type Reaction Promoted by a New Heterobimetallic Complex
Yamada, K.-i., The First Catalytic Asymmetric Nitro-Mannich-type Reaction Promoted by a New Heterobimetallic Complex. Angew. Chem. Int.Ed. 38 (). , 1999
PUB
 
[23]
1999 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2407545
Towards Perfect Asymmetric Catalysis: Additives and Co-catalysts
Vogl, E.M, Towards Perfect Asymmetric Catalysis: Additives and Co-catalysts. Angew. Chem. Int. Ed. 38 (11). , 1999
PUB | DOI | WoS | PubMed | Europe PMC
 
[22]
1999 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2347907
Chiral Heterobimetallic Lanthanoid Complexes: A Highly Efficient Multifunctional Catalyst for the Asymmetric Formation of C-C,C-O, and C-P Bonds
Shibasaki, M., Chiral Heterobimetallic Lanthanoid Complexes: A Highly Efficient Multifunctional Catalyst for the Asymmetric Formation of C-C,C-O, and C-P Bonds. Topics in Organometallic Chemistry: Lanthanides: Chemistry and Use in Organic Synthesis 2 (). Heidelberg, 1999
PUB
 
[21]
1999 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2407465
Erste katalytische asymmetrische Nitro-Mannich-Reaktion mit einem neuen Heterodimetallkomplex des Katalysators
Yamada, Ken-ichi, Erste katalytische asymmetrische Nitro-Mannich-Reaktion mit einem neuen Heterodimetallkomplex des Katalysators. Angewandte Chem. (111). , 1999
PUB
 
[20]
1999 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2407462
Zur Perfektionierung der asymmetrischen Katalyse: Additive und Co-Katalysatoren
Vogl, Erasmus M., Zur Perfektionierung der asymmetrischen Katalyse: Additive und Co-Katalysatoren. Angew. Chem. (111). , 1999
PUB
 
[19]
1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347854
The First Synthesis of Cyclic alpha-Amino Phosphonic Acid Amines Bearing the Benzodiazaphosphorinananone System
Gröger, Harald, The First Synthesis of Cyclic alpha-Amino Phosphonic Acid Amines Bearing the Benzodiazaphosphorinananone System. Heteroatom Chem. 9 (). , 1998
PUB
 
[18]
1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347865
A New and Highly Efficient Route to Cyclic alpha-Amino Phosphonates: The First Catalytic Enantioselective Hydrophosphonylation of Cyclic Imines Catalyzed by Chiral Heterobimetallic Lanthanoid Complexes
Gröger, Harald, A New and Highly Efficient Route to Cyclic alpha-Amino Phosphonates: The First Catalytic Enantioselective Hydrophosphonylation of Cyclic Imines Catalyzed by Chiral Heterobimetallic Lanthanoid Complexes. J. Am. Chem. Soc. 120 (). , 1998
PUB
 
[17]
1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347881
New Catalytic Concepts for the Asymmetric Aldol Reaction
Gröger, Harald, New Catalytic Concepts for the Asymmetric Aldol Reaction. Chem. Eur. J. 4 (). , 1998
PUB
 
[16]
1997 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347828
A Novel Synthetic Approach to alpha-Aminophosphine Sulfide Structures: The First Dimethylphosphine Sulfide Addition to 3-Thiazolines
Gröger, Harald, A Novel Synthetic Approach to alpha-Aminophosphine Sulfide Structures: The First Dimethylphosphine Sulfide Addition to 3-Thiazolines. Phosphorus, Sulfur, Silicon 128 (). , 1997
PUB
 
[15]
1997 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347743
Synthesis and Applilcation of New ß-Amino Alcohols Based on the Octahydrocyclopenta[b]pyrrol System in the Catalytic Enantioselective Addition of Diethylzinc to Benzaldehyde
Wilken, J., Synthesis and Applilcation of New ß-Amino Alcohols Based on the Octahydrocyclopenta[b]pyrrol System in the Catalytic Enantioselective Addition of Diethylzinc to Benzaldehyde. Tetrahedron: Asymmetry 8 (). , 1997
PUB
 
[14]
1997 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347713
Synthesis of Dimethyl 4-Thiazolidinylphosphine Oxides via Addition of Dimethylphosphine Oxide to 3-Thiazolines
Gröger, Harald, Synthesis of Dimethyl 4-Thiazolidinylphosphine Oxides via Addition of Dimethylphosphine Oxide to 3-Thiazolines. Heteroatom Chem. 8 (). , 1997
PUB
 
[13]
1997 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347775
Synthesis and Application of New (threo)- and (erythro)-Amino Alcohols Based on the Octahydro-cyclopenta[b]pyrrol System in the Catalytic Enantioselective Addition of Diethylzinc to Benzaldehyde
Wilken, J., Synthesis and Application of New (threo)- and (erythro)-Amino Alcohols Based on the Octahydro-cyclopenta[b]pyrrol System in the Catalytic Enantioselective Addition of Diethylzinc to Benzaldehyde. Tetrahedron Asymmetry 8 (). , 1997
PUB
 
[12]
1997 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347821
A New Enantioselective Synthetic Approach to ß-Aminothio-compounds via Enantioselective Reduction of N,S-Heterocyclic Imines
Reiners, I., A New Enantioselective Synthetic Approach to ß-Aminothio-compounds via Enantioselective Reduction of N,S-Heterocyclic Imines. J. Prakt. Chem. 339 (). , 1997
PUB
 
[11]
1997 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347759
Synthesis of New, Chiral ß-sec-Amino Alcohols - Diastereodivergent Addition of Grignard-Reagents to a-Amno Aldehydes Based on the (all-R)-2-Azabicyclo[3.3.0]octane-System
Wilken, J., Synthesis of New, Chiral ß-sec-Amino Alcohols - Diastereodivergent Addition of Grignard-Reagents to a-Amno Aldehydes Based on the (all-R)-2-Azabicyclo[3.3.0]octane-System. Liebigs Ann./Recuell (). , 1997
PUB
 
[10]
1997 | Diskussionspapier | Veröffentlicht | PUB-ID: 2347850
Nukleophile Additionsreaktionen an die C=N-Doppelbindung schwefelhaltiger, cyclischer Imine unter Berücksichtigung stereoselektiver Aspekte
Gröger, Harald, Nukleophile Additionsreaktionen an die C=N-Doppelbindung schwefelhaltiger, cyclischer Imine unter Berücksichtigung stereoselektiver Aspekte. (). , 1997
PUB
 
[9]
1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347671
The Totally Protected Hydroxy Containing alpha-Amino Phosphonic Esters and alpha-Amino Phosphinoxides as well as their Carbamoyl Derivatives
Hatam, M., The Totally Protected Hydroxy Containing alpha-Amino Phosphonic Esters and alpha-Amino Phosphinoxides as well as their Carbamoyl Derivatives. Synth. Commun. 26 (). , 1996
PUB
 
[8]
1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344573
Synthese Totalgeschützter Thioanaloga der 1,2,3,4-Tetrahydrochinolin-2-carbonsäure aus 2H-1,4-Benzothiazinen via Ugi-Reaktion
Gröger, Harald, Synthese Totalgeschützter Thioanaloga der 1,2,3,4-Tetrahydrochinolin-2-carbonsäure aus 2H-1,4-Benzothiazinen via Ugi-Reaktion. Sulfur Lett. 19 (). , 1996
PUB
 
[7]
1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347651
Chemistry of the 1,3,5-Triaza-2-phosphorine-4,6-diones, Part XI. Base-Catalyzed Addition Reactions of 2-Oxo-2-hydro-1,3,5-trimethyl-1,3,5-triaza-2I4-phosphorine-4,6-dione to the C-N Double Bond of 3-Thiazoline Heterocycles
Neda, I., Chemistry of the 1,3,5-Triaza-2-phosphorine-4,6-diones, Part XI. Base-Catalyzed Addition Reactions of 2-Oxo-2-hydro-1,3,5-trimethyl-1,3,5-triaza-2I4-phosphorine-4,6-dione to the C-N Double Bond of 3-Thiazoline Heterocycles. Z. Naturforsch. 51b (). , 1996
PUB
 
[6]
1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344556
Synthesis of New 4-Thiazolidinylphosphonates via Stereoselective Pudovik Reaction
Gröger, Harald, Synthesis of New 4-Thiazolidinylphosphonates via Stereoselective Pudovik Reaction. Synth. Commun. 26 (). , 1996
PUB
 
[5]
1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344599
Synthetic Approach to New alpha-Aminophosphonates Derived from Six-Membered, Sulfur-Containing Heterocyclic Imines
Gröger, Harald, Synthetic Approach to New alpha-Aminophosphonates Derived from Six-Membered, Sulfur-Containing Heterocyclic Imines. Phosphorus, Sulfur, Silicon 116 (). , 1996
PUB
 
[4]
1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347629
Stereoselektive Pudovik-Reaktion von 5,6-Benzo-2H-1-methyl-3-(2'-chlorethyl)-2-oxo-1,3,2I4-diazaphosphorin-4-on mit einem 3-Thiazolin und MPL-Chromatographische Isolierung des Überschußdiastereomers
Gröger, Harald, Stereoselektive Pudovik-Reaktion von 5,6-Benzo-2H-1-methyl-3-(2'-chlorethyl)-2-oxo-1,3,2I4-diazaphosphorin-4-on mit einem 3-Thiazolin und MPL-Chromatographische Isolierung des Überschußdiastereomers. Z. Naturforsch. 51b (). , 1996
PUB
 
[3]
1996 | Zeitschriftenaufsatz | PUB-ID: 2344586
Synthesis of Glutathione Analogues, Peptide Nucleic Acids and Phosphono-oligopetides from Heterocyclic Imines
Gröger, Harald, Synthesis of Glutathione Analogues, Peptide Nucleic Acids and Phosphono-oligopetides from Heterocyclic Imines. Synth. Commun. 26 (). , 1996
PUB
 
[2]
1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347696
First Catalytic Asymmetric Hydrophosphonylation of Cyclilc Imines: Highly Efficient Enantioselective Approach to a 4-Thiazolidinylphosphonate via Chiral Titanium and Lanthanoid Catalysts
Gröger, Harald, First Catalytic Asymmetric Hydrophosphonylation of Cyclilc Imines: Highly Efficient Enantioselective Approach to a 4-Thiazolidinylphosphonate via Chiral Titanium and Lanthanoid Catalysts. Tetrahedron Lett. 37 (). , 1996
PUB
 
[1]
1995 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344535
Synthese Totalgeschützter, Nichtproteinogener alpha-Aminosäuren und Oligopeptide aus 2H-1,3-Oxazinen und 2H-1,3-Bezoxazinen via Ugi-Reaction
Gröger, Harald, Synthese Totalgeschützter, Nichtproteinogener alpha-Aminosäuren und Oligopeptide aus 2H-1,3-Oxazinen und 2H-1,3-Bezoxazinen via Ugi-Reaction. Tetrahedron 51 (). , 1995
PUB
 

Suche

Publikationen filtern

Darstellung / Sortierung

Zitationsstil: default

Export / Einbettung

236 Publikationen

Alle markieren

[236]
2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2936254
Isolation and characterization of side-products formed through ∆2-isomerization in the synthesis of cefpodoxime proxetil.
Pieper, Matthias, Isolation and characterization of side-products formed through ∆2-isomerization in the synthesis of cefpodoxime proxetil.. The Journal of antibiotics (). , 2019
PUB | DOI | PubMed | Europe PMC
 
[235]
2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2936145
Cyanide-free synthesis of an aromatic nitrile from a biorenewable-based aldoxime: Development and application of a recombinant aldoxime dehydratase as a biocatalyst
Choi, Ji-Eun, Cyanide-free synthesis of an aromatic nitrile from a biorenewable-based aldoxime: Development and application of a recombinant aldoxime dehydratase as a biocatalyst. BIOCATALYSIS AND BIOTRANSFORMATION (). , 2019
PUB | DOI | WoS
 
[234]
2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2935493
Asymmetric Formal Synthesis of (+)-Catharanthine via Desymmetrization of Isoquinuclidine.
Kono, Masato, Asymmetric Formal Synthesis of (+)-Catharanthine via Desymmetrization of Isoquinuclidine.. Organic letters 21 (10). , 2019
PUB | DOI | WoS | PubMed | Europe PMC
 
[233]
2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2935205
Chemoenzymatic Synthesis of a Chiral Ozanimod Key Intermediate Starting from Naphthalene as Cheap Petrochemical Feedstock.
Uthoff, Florian, Chemoenzymatic Synthesis of a Chiral Ozanimod Key Intermediate Starting from Naphthalene as Cheap Petrochemical Feedstock.. The Journal of organic chemistry 84 (8). , 2019
PUB | DOI | WoS | PubMed | Europe PMC
 
[232]
2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2933178
Biocatalytic Reduction of 2-Monosubstituted 3-Thiazolines Using Imine Reductases
Zumbrägel, Nadine, Biocatalytic Reduction of 2-Monosubstituted 3-Thiazolines Using Imine Reductases. Journal of Heterocyclic Chemistry (). , 2019
PUB | DOI | WoS
 
[231]
2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2934545
Detection and fragmentation of doubly charged peptide ions in MALDI-Q-TOF-MS by ion mobility spectrometry for improved protein identification.
Sproß, Jens, Detection and fragmentation of doubly charged peptide ions in MALDI-Q-TOF-MS by ion mobility spectrometry for improved protein identification.. Analytical and bioanalytical chemistry (). , 2019
PUB | DOI | PubMed | Europe PMC
 
[230]
2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2934606
Catalysts Encapsulated in Biopolymer Hydrogels for Chemoenzymatic One-Pot Processes in Aqueous Media
Pauly, Jan, Catalysts Encapsulated in Biopolymer Hydrogels for Chemoenzymatic One-Pot Processes in Aqueous Media. CHEMCATCHEM 11 (5). , 2019
PUB | DOI | WoS
 
[229]
2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2934607
Enantioselective One-Pot Synthesis of Biaryl-Substituted Amines by Combining Palladium and Enzyme Catalysis in Deep Eutectic Solvents
Paris, Juraj, Enantioselective One-Pot Synthesis of Biaryl-Substituted Amines by Combining Palladium and Enzyme Catalysis in Deep Eutectic Solvents. ACS SUSTAINABLE CHEMISTRY & ENGINEERING 7 (5). , 2019
PUB | DOI | WoS
 
[228]
2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2933685
Type II flavoprotein monooxygenase PsFMO_A from the bacterium Pimelobacter sp. Bb-B catalyzes enantioselective Baeyer-Villiger oxidations with a relaxed cofactor specificity.
Löwe, Jana, Type II flavoprotein monooxygenase PsFMO_A from the bacterium Pimelobacter sp. Bb-B catalyzes enantioselective Baeyer-Villiger oxidations with a relaxed cofactor specificity.. Journal of biotechnology (). , 2019
PUB | DOI | WoS | PubMed | Europe PMC
 
[227]
2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2934376
An Asymmetric Organocatalytic Aldol Reaction of a Hydrophobic Aldehyde in Aqueous Medium Running in Flow Mode
Schober, Lukas, An Asymmetric Organocatalytic Aldol Reaction of a Hydrophobic Aldehyde in Aqueous Medium Running in Flow Mode. SYNTHESIS-STUTTGART 51 (5). , 2019
PUB | DOI | WoS
 
[226]
2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2934122
Amine Transaminase from Exophiala Xenobiotica-Crystal Structure and Engineering of a Fold IV Transaminase that Naturally Converts Biaryl Ketones
Telzerow, Aline, Amine Transaminase from Exophiala Xenobiotica-Crystal Structure and Engineering of a Fold IV Transaminase that Naturally Converts Biaryl Ketones. ACS CATALYSIS 9 (2). , 2019
PUB | DOI | WoS
 
[225]
2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2933300
Biocatalytic concepts for synthesizing amine bulk chemicals: recent approaches towards linear and cyclic aliphatic primary amines and substituted derivatives thereof
Gröger, Harald, Biocatalytic concepts for synthesizing amine bulk chemicals: recent approaches towards linear and cyclic aliphatic primary amines and substituted derivatives thereof. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY 103 (1). , 2019
PUB | DOI | WoS | PubMed | Europe PMC
 
[224]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2921159
Providing reducing power by microalgal photosynthesis: a novel perspective towards sustainable biocatalytic production of bulk chemicals exemplified for aliphatic amines
Löwe, Jana, Providing reducing power by microalgal photosynthesis: a novel perspective towards sustainable biocatalytic production of bulk chemicals exemplified for aliphatic amines. Scientific Reports 8 (1). , 2018
PUB | PDF | DOI | WoS | PubMed | Europe PMC
 
[223]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2932504
Biocatalytic production of adiponitrile and related aliphatic linear α,ω-dinitriles
Betke, Tobias, Biocatalytic production of adiponitrile and related aliphatic linear α,ω-dinitriles. Nature Communications 9 (). , 2018
PUB | PDF | DOI | WoS | PubMed | Europe PMC
 
[222]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2930227
Merging Heterocyclic Chemistry and Biocatalysis in One-Pot Processes through Compartmentalization of the Reaction Steps
Zumbrägel, Nadine, Merging Heterocyclic Chemistry and Biocatalysis in One-Pot Processes through Compartmentalization of the Reaction Steps. Bioengineering 5 (). , 2018
PUB | PDF | DOI | PubMed | Europe PMC
 
[221]
2018 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2933180
Chiral Dinuclear Vanadium Complex-Mediated Oxidative Coupling of Resorcinols
Sako, Makoto, Chiral Dinuclear Vanadium Complex-Mediated Oxidative Coupling of Resorcinols. The Journal of Organic Chemistry (). , 2018
PUB | DOI | WoS | PubMed | Europe PMC
 
[220]
2018 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2933177
Enantioselective Biocatalytic Reduction of 2H-1,4-Benzoxazines Using Imine Reductases
Zumbrägel, Nadine, Enantioselective Biocatalytic Reduction of 2H-1,4-Benzoxazines Using Imine Reductases. The Journal of Organic Chemistry (). , 2018
PUB | DOI | WoS | PubMed | Europe PMC
 
[219]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2933928
The function of the oxylipin 12-oxophytodienoic acid in cell signaling, stress acclimation, and development
Maynard, Daniel, The function of the oxylipin 12-oxophytodienoic acid in cell signaling, stress acclimation, and development. JOURNAL OF EXPERIMENTAL BOTANY 69 (22). , 2018
PUB | DOI | WoS | PubMed | Europe PMC
 
[218]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2933179
One-pot synthesis of a 3-thiazolidine through combination of an Asinger-type multi-component-condensation reaction with an enzymatic imine reduction
Zumbrägel, Nadine, One-pot synthesis of a 3-thiazolidine through combination of an Asinger-type multi-component-condensation reaction with an enzymatic imine reduction. Journal of Biotechnology 291 (). , 2018
PUB | DOI | WoS | PubMed | Europe PMC
 
[217]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2932766
Metathesis in water conducted by tailor-made encapsulated Grubbs' catalyst
Pauly, Jan, Metathesis in water conducted by tailor-made encapsulated Grubbs' catalyst. GREEN CHEMISTRY 20 (22). , 2018
PUB | DOI | WoS
 
[216]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2919867
Enantioselective reduction of sulfur-containing cyclic imines through biocatalysis
Zumbrägel, Nadine, Enantioselective reduction of sulfur-containing cyclic imines through biocatalysis. Nature Communications 9 (). , 2018
PUB | DOI | WoS | PubMed | Europe PMC
 
[215]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2931977
Novel Insights into the Combination of Metal- and Biocatalysis: Cascade One-Pot Synthesis of Enantiomerically Pure Biaryl Alcohols in Deep Eutectic Solvents
Paris, Juraj, Novel Insights into the Combination of Metal- and Biocatalysis: Cascade One-Pot Synthesis of Enantiomerically Pure Biaryl Alcohols in Deep Eutectic Solvents. CHEMCATCHEM 10 (19). , 2018
PUB | DOI | WoS
 
[214]
2018 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2920724
Design, characterisation and application of alginate-based encapsulated pig liver esterase
Pauly, Jan, Design, characterisation and application of alginate-based encapsulated pig liver esterase. Journal of Biotechnology 280 (). , 2018
PUB | Dateien verfügbar | DOI | WoS | PubMed | Europe PMC
 
[213]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2931244
Stereoselective synthesis of enantiomerically pure bowl-shaped hydroxytribenzotriquinacenes
Rommelmann, Philipp, Stereoselective synthesis of enantiomerically pure bowl-shaped hydroxytribenzotriquinacenes. ORGANIC & BIOMOLECULAR CHEMISTRY 16 (31). , 2018
PUB | DOI | WoS | PubMed | Europe PMC
 
[212]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2931119
Process Development for Synthesizing the Cephalosporin Antibiotic Cefotaxime in Batch and Flow Mode
Pieper, Matthias, Process Development for Synthesizing the Cephalosporin Antibiotic Cefotaxime in Batch and Flow Mode. ORGANIC PROCESS RESEARCH & DEVELOPMENT 22 (8). , 2018
PUB | DOI | WoS
 
[211]
2018 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2930305
Vanadium-Catalyzed Dehydrogenation of N-Heterocycles in Water
Zumbrägel, Nadine, Vanadium-Catalyzed Dehydrogenation of N-Heterocycles in Water. Organic Letters 20 (16). , 2018
PUB | DOI | WoS | PubMed | Europe PMC
 
[210]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2931113
Asymmetric Synthesis of 1-Phenylethylamine from Styrene via Combined Wacker Oxidation and Enzymatic Reductive Amination
Uthoff, Florian, Asymmetric Synthesis of 1-Phenylethylamine from Styrene via Combined Wacker Oxidation and Enzymatic Reductive Amination. JOURNAL OF ORGANIC CHEMISTRY 83 (16). , 2018
PUB | DOI | WoS | PubMed | Europe PMC
 
[209]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920277
Enantioselective synthesis of amines via reductive amination with a dehydrogenase mutant from Exigobacterium sibiricum: Substrate scope, co-solvent tolerance and biocatalyst immobilization
Löwe, Jana, Enantioselective synthesis of amines via reductive amination with a dehydrogenase mutant from Exigobacterium sibiricum: Substrate scope, co-solvent tolerance and biocatalyst immobilization. BIOORGANIC & MEDICINAL CHEMISTRY 26 (7). , 2018
PUB | DOI | WoS | PubMed | Europe PMC
 
[208]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2913715
One-pot synthesis of bioactive cyclopentenones from α-linolenic acid and docosahexaenoic acid
Maynard, Daniel, One-pot synthesis of bioactive cyclopentenones from α-linolenic acid and docosahexaenoic acid. Bioorganic & Medicinal Chemistry 26 (7). , 2018
PUB | DOI | WoS | PubMed | Europe PMC
 
[207]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916923
Biocatalytic Synthesis of Nitriles through Dehydration of Aldoximes: The Substrate Scope of Aldoxime Dehydratases
Betke, Tobias, Biocatalytic Synthesis of Nitriles through Dehydration of Aldoximes: The Substrate Scope of Aldoxime Dehydratases. ChemBioChem 19 (8). , 2018
PUB | DOI | WoS | PubMed | Europe PMC
 
[206]
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2919325
Opportunities and challenges for combining chemo- and biocatalysis
Rudroff, Florian, Opportunities and challenges for combining chemo- and biocatalysis. NATURE CATALYSIS 1 (1). , 2018
PUB | DOI | WoS
 
[205]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2913114
Cyanide-Free and Broadly Applicable Enantioselective Synthetic Platform for Chiral Nitriles through a Biocatalytic Approach
Betke, Tobias, Cyanide-Free and Broadly Applicable Enantioselective Synthetic Platform for Chiral Nitriles through a Biocatalytic Approach. Angewandte Chemie (International ed. in English) 46 (40). , 2017
PUB | DOI | WoS | PubMed | Europe PMC
 
[204]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916530
Industrial landmarksinthedevelopmentofsustainableproduction processesforthe beta-lactam antibiotickeyintermediate 7-aminocephalosporanic acid (7-ACA)
Gröger, Harald, Industrial landmarksinthedevelopmentofsustainableproduction processesforthe beta-lactam antibiotickeyintermediate 7-aminocephalosporanic acid (7-ACA). SUSTAINABLE CHEMISTRY AND PHARMACY 5 (). , 2017
PUB | DOI | WoS
 
[203]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2910386
Process Development through Solvent Engineering in the Biocatalytic Synthesis of the Heterocyclic Bulk Chemical epsilon-Caprolactone
Reimer, Anna, Process Development through Solvent Engineering in the Biocatalytic Synthesis of the Heterocyclic Bulk Chemical epsilon-Caprolactone. JOURNAL OF HETEROCYCLIC CHEMISTRY 54 (1). , 2017
PUB | DOI | WoS
 
[202]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2911773
"Side-Product Catalysis": Substrate Autoxidation as an Overlooked Side Reaction Generating a Co-Catalyst for Enhancing Asymmetric Aldol Reactions
Heidlindemann, Marcel, "Side-Product Catalysis": Substrate Autoxidation as an Overlooked Side Reaction Generating a Co-Catalyst for Enhancing Asymmetric Aldol Reactions. CHEMCATCHEM 9 (8). , 2017
PUB | DOI | WoS
 
[201]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909081
First Tandem-Type One-Pot Process Combining Asymmetric Organo- and Biocatalytic Reactions in Aqueous Media Exemplified for the Enantioselective and Diastereoselective Synthesis of 1,3-Diols
Rulli, Giuseppe, First Tandem-Type One-Pot Process Combining Asymmetric Organo- and Biocatalytic Reactions in Aqueous Media Exemplified for the Enantioselective and Diastereoselective Synthesis of 1,3-Diols. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY 2017 (4). , 2017
PUB | DOI | WoS
 
[200]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2908557
Recombinant expression and characterization of a l-amino acid oxidase from the fungus Rhizoctonia solani
Hahn, Katharina, Recombinant expression and characterization of a l-amino acid oxidase from the fungus Rhizoctonia solani. Applied Microbiology and Biotechnology 101 (7). , 2017
PUB | DOI | WoS | PubMed | Europe PMC
 
[199]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2910338
An alternative approach towards poly-epsilon-caprolactone through a chemoenzymatic synthesis: combined hydrogenation, bio-oxidations and polymerization without the isolation of intermediates
Wedde, Severin, An alternative approach towards poly-epsilon-caprolactone through a chemoenzymatic synthesis: combined hydrogenation, bio-oxidations and polymerization without the isolation of intermediates. GREEN CHEMISTRY 19 (5). , 2017
PUB | DOI | WoS
 
[198]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2910354
Formal Enantioselective Hydroamination of Non-Activated Alkenes: Transformation of Styrenes into Enantiomerically Pure 1-Phenylethylamines in Chemoenzymatic One-Pot Synthesis
Uthoff, Florian, Formal Enantioselective Hydroamination of Non-Activated Alkenes: Transformation of Styrenes into Enantiomerically Pure 1-Phenylethylamines in Chemoenzymatic One-Pot Synthesis. CHEMCATCHEM 9 (4). , 2017
PUB | DOI | WoS
 
[197]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2908777
Kinetic insights into ϵ-caprolactone synthesis: Improvement of an enzymatic cascade reaction
Scherkus, Christian, Kinetic insights into ϵ-caprolactone synthesis: Improvement of an enzymatic cascade reaction. Biotechnology and Bioengineering 114 (6). , 2017
PUB | DOI | WoS | PubMed | Europe PMC
 
[196]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916529
Enzymatic resolution of an amine under solvent-free conditions with diethyl malonate as reagent for acylation
Uthoff, Florian, Enzymatic resolution of an amine under solvent-free conditions with diethyl malonate as reagent for acylation. SUSTAINABLE CHEMISTRY AND PHARMACY 5 (). , 2017
PUB | DOI | WoS
 
[195]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2914659
High-throughput-feasible screening tool for determining enzyme stabilities against organic solvents directly from crude extracts
Wedde, Severin, High-throughput-feasible screening tool for determining enzyme stabilities against organic solvents directly from crude extracts. Chembiochem : a European journal of chemical biology 18 (24). , 2017
PUB | DOI | WoS | PubMed | Europe PMC
 
[194]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2912688
ASYMMETRIC BIOCATALYTIC REDUCTION OF CYCLIC IMINES: DESIGN AND APPLICATION OF A TAILOR-MADE WHOLE-CELL CATALYST
Zumbrägel, Nadine, ASYMMETRIC BIOCATALYTIC REDUCTION OF CYCLIC IMINES: DESIGN AND APPLICATION OF A TAILOR-MADE WHOLE-CELL CATALYST. HETEROCYCLES 95 (2). , 2017
PUB | DOI | WoS
 
[193]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916457
Synthesis of Enantiomerically Pure N-Acyl Amino Nitriles via Catalytic Dehydration of Oximes and Application in a de Novo Synthesis of Vildagliptin
Rommelmann, Philipp, Synthesis of Enantiomerically Pure N-Acyl Amino Nitriles via Catalytic Dehydration of Oximes and Application in a de Novo Synthesis of Vildagliptin. Organic Process Research & Development 21 (10). , 2017
PUB | DOI | WoS
 
[192]
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909084
Design of recombinant whole-cell catalysts for double reduction of C=C and C=O bonds in enals and application in the synthesis of Guerbet alcohols as industrial bulk chemicals for lubricants
Biermann, Marc, Design of recombinant whole-cell catalysts for double reduction of C=C and C=O bonds in enals and application in the synthesis of Guerbet alcohols as industrial bulk chemicals for lubricants. GREEN CHEMISTRY 19 (2). , 2017
PUB | DOI | WoS
 
[191]
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2904890
Screening, Molecular Cloning, and Biochemical Characterization of an Alcohol Dehydrogenase from Pichia pastoris Useful for the Kinetic Resolution of a Racemic β-Hydroxy-β-trifluoromethyl Ketone
Bulut, Dalia, Screening, Molecular Cloning, and Biochemical Characterization of an Alcohol Dehydrogenase from Pichia pastoris Useful for the Kinetic Resolution of a Racemic β-Hydroxy-β-trifluoromethyl Ketone. Chembiochem 17 (14). , 2016
PUB | DOI | WoS | PubMed | Europe PMC
 
[190]
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2907316
A whole cell biocatalyst for double oxidation of cyclooctane
Müller, C. A., A whole cell biocatalyst for double oxidation of cyclooctane. Journal of Industrial Microbiology & Biotechnology 43 (12). , 2016
PUB | DOI | WoS | PubMed | Europe PMC
 
[189]
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2906851
A One-Pot Cascade Reaction Combining an Encapsulated Decarboxylase with a Metathesis Catalyst for the Synthesis of Bio-Based Antioxidants
Gómez Baraibar, Álvaro, A One-Pot Cascade Reaction Combining an Encapsulated Decarboxylase with a Metathesis Catalyst for the Synthesis of Bio-Based Antioxidants. Angewandte Chemie International Edition 55 (47). , 2016
PUB | DOI | WoS | PubMed | Europe PMC
 
[188]
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2906192
Shibasaki Catalysts and Their Use for Asymmetric Synthetic Applications by the Chemical Industry
Gröger, Harald, Shibasaki Catalysts and Their Use for Asymmetric Synthetic Applications by the Chemical Industry. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY (24). , 2016
PUB | DOI | WoS
 
[187]
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2917152
Guerbet Alcohols: From Processes under Harsh Conditions to Synthesis at Room Temperature under Ambient Pressure
Biermann, Marc, Guerbet Alcohols: From Processes under Harsh Conditions to Synthesis at Room Temperature under Ambient Pressure. CHEMCATCHEM 8 (5). , 2016
PUB | DOI | WoS
 
[186]
2016 | Konferenzbeitrag | Veröffentlicht | PUB-ID: 2908647
Nano/Microfluidic Devices for Whole-Cell Biocatalyst Analysis by UV/VIS-Spectroscopy
Viefhues, Martina, Nano/Microfluidic Devices for Whole-Cell Biocatalyst Analysis by UV/VIS-Spectroscopy. Proceedings of the 20. International Conference on Miniaturized Systems for Chemistry and Life Sciences 2016 (µTAS 2016) (). Dublin, Irland, 2016
PUB
 
[185]
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2907726
A Fed-Batch Synthetic Strategy for a Three-Step Enzymatic Synthesis of Poly-epsilon-caprolactone
Scherkus, Christian, A Fed-Batch Synthetic Strategy for a Three-Step Enzymatic Synthesis of Poly-epsilon-caprolactone. CHEMCATCHEM 8 (22). , 2016
PUB | DOI | WoS
 
[184]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2785615
Olefin Metathesis Reaction in Water and in Air Improved by Supramolecular Additives
Tomasek, Jasmine, Olefin Metathesis Reaction in Water and in Air Improved by Supramolecular Additives. Molecules 20 (10). , 2015
PUB | DOI | WoS | PubMed | Europe PMC
 
[183]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2901254
Biocatalytic access to chiral polyesters by an artificial enzyme cascade synthesis
Schmidt, Sandy, Biocatalytic access to chiral polyesters by an artificial enzyme cascade synthesis. ChemCatChem 7 (23). , 2015
PUB | DOI | WoS
 
[182]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2773289
Synthesis of substituted cycloalkene-1,1-dicarboxylates via olefin metathesis in water
Tenbrink, Katharina, Synthesis of substituted cycloalkene-1,1-dicarboxylates via olefin metathesis in water. ARKIVOC (). , 2015
PUB | DOI | WoS
 
[181]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2764353
Integrated Biocatalysis in Multistep Drug Synthesis without Intermediate Isolation: A de Novo Approach toward a Rosuvastatin Key Building Block
Metzner, Richard, Integrated Biocatalysis in Multistep Drug Synthesis without Intermediate Isolation: A de Novo Approach toward a Rosuvastatin Key Building Block. Organic Process Research & Development 19 (6). , 2015
PUB | DOI | WoS
 
[180]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2719049
Iron(III)-porphyrin Complex FeTSPP: A Versatile Water-soluble Catalyst for Oxidations in Organic Syntheses, Biorenewables Degradation and Environmental Applications
Böhm, Philipp, Iron(III)-porphyrin Complex FeTSPP: A Versatile Water-soluble Catalyst for Oxidations in Organic Syntheses, Biorenewables Degradation and Environmental Applications. ChemCatChem 7 (1). , 2015
PUB | DOI | WoS
 
[179]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2757961
Vanadium in asymmetric synthesis: emerging concepts in catalyst design and applications
Takizawa, Shinobu, Vanadium in asymmetric synthesis: emerging concepts in catalyst design and applications. Chemistry 21 (25). , 2015
PUB | DOI | WoS | PubMed | Europe PMC
 
[178]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2721884
An Enzyme Cascade Synthesis of ε-Caprolactone and its Oligomers
Schmidt, Sandy, An Enzyme Cascade Synthesis of ε-Caprolactone and its Oligomers. Angewandte Chemie (International ed. in English) 54 (9). , 2015
PUB | DOI | WoS | PubMed | Europe PMC
 
[177]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2729781
Cooperative Catalysis of Noncompatible Catalysts through Compartmentalization: Wacker Oxidation and Enzymatic Reduction in a One-Pot Process in Aqueous Media
Sato, Hirofumi, Cooperative Catalysis of Noncompatible Catalysts through Compartmentalization: Wacker Oxidation and Enzymatic Reduction in a One-Pot Process in Aqueous Media. Angewandte Chemie (International ed. in English) 54 (15). , 2015
PUB | DOI | WoS | PubMed | Europe PMC
 
[176]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2786832
Enantiomerically Pure Tribenzotriquinacenes through Stereoselective Synthesis
Greschner, Wilko, Enantiomerically Pure Tribenzotriquinacenes through Stereoselective Synthesis. Angewandte Chemie (International ed. in English) 54 (46). , 2015
PUB | DOI | WoS | PubMed | Europe PMC
 
[175]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2773287
Professor Dr. Jürgen Martens A tribute
Gröger, Harald, Professor Dr. Jürgen Martens A tribute. ARKIVOC (). , 2015
PUB | WoS
 
[174]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2758474
The Organic-Synthetic Potential of Recombinant Ene Reductases: Substrate-Scope Evaluation and Process Optimization
Reß, Tina, The Organic-Synthetic Potential of Recombinant Ene Reductases: Substrate-Scope Evaluation and Process Optimization. ChemCatChem 7 (8). , 2015
PUB | DOI | WoS
 
[173]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2761249
Development of a growth-dependent selection system for identification of L-threonine aldolases
Bulut, Dalia, Development of a growth-dependent selection system for identification of L-threonine aldolases. Applied Microbiology and Biotechnology 99 (14). , 2015
PUB | DOI | WoS | PubMed | Europe PMC
 
[172]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2729792
Chemoenzymatic Synthesis of Vitamin B5-Intermediate (R)-Pantolactone via Combined Asymmetric Organo- and Biocatalysis
Heidlindemann, Marcel, Chemoenzymatic Synthesis of Vitamin B5-Intermediate (R)-Pantolactone via Combined Asymmetric Organo- and Biocatalysis. The Journal of Organic Chemistry 80 (7). , 2015
PUB | DOI | WoS | PubMed | Europe PMC
 
[171]
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2690890
Combination of Asymmetric Organo- and Biocatalytic Reactions in Organic Media Using Immobilized Catalysts in Different Compartments
Heidlindemann, Marcel, Combination of Asymmetric Organo- and Biocatalytic Reactions in Organic Media Using Immobilized Catalysts in Different Compartments. ACS Catalysis 4 (4). , 2014
PUB | DOI | WoS
 
[170]
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2707682
Cyanide-free Enantioselective Synthesis of Nitriles: Synthetic Proof of a Biocatalytic Concept and Mechanistic Insights
Metzner, Richard, Cyanide-free Enantioselective Synthesis of Nitriles: Synthetic Proof of a Biocatalytic Concept and Mechanistic Insights. ChemCatChem 6 (11). , 2014
PUB | DOI | WoS
 
[169]
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2708851
Strategies for regeneration of nicotinamide coenzymes emphasizing self-sufficient closed-loop recycling systems
Hummel, Werner, Strategies for regeneration of nicotinamide coenzymes emphasizing self-sufficient closed-loop recycling systems. Journal of biotechnology 191 (). , 2014
PUB | DOI | WoS | PubMed | Europe PMC
 
[168]
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2708863
Whole-cell double oxidation of n-heptane
Müller, Christina A., Whole-cell double oxidation of n-heptane. Journal of biotechnology 191 (). , 2014
PUB | DOI | WoS | PubMed | Europe PMC
 
[167]
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2681761
Artificial cofactor regeneration with an iron(III)porphyrin as NADH-oxidase mimic in the enzymatic oxidation of L-glutamate to alpha-ketoglutarate
Greschner, Wilko, Artificial cofactor regeneration with an iron(III)porphyrin as NADH-oxidase mimic in the enzymatic oxidation of L-glutamate to alpha-ketoglutarate. Journal of Molecular Catalysis B Enzymatic 103 (). , 2014
PUB | DOI | WoS
 
[166]
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2699267
Enzymatic resolution of racemates with a 'remote' stereogenic center as an efficient tool in drug, flavor and vitamin synthesis
Alfaro Blasco, Maria, Enzymatic resolution of racemates with a 'remote' stereogenic center as an efficient tool in drug, flavor and vitamin synthesis. Bioorganic & medicinal chemistry 22 (20). , 2014
PUB | DOI | WoS | PubMed | Europe PMC
 
[165]
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2682298
Combining the 'two worlds' of chemocatalysis and biocatalysis towards multi-step one-pot processes in aqueous media
Gröger, Harald, Combining the 'two worlds' of chemocatalysis and biocatalysis towards multi-step one-pot processes in aqueous media. Current opinion in chemical biology 19 (). , 2014
PUB | DOI | WoS | PubMed | Europe PMC
 
[164]
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2677387
Enantioselective Rearrangement Coupled with Water Addition: Direct Synthesis of Enantiomerically Pure Saturated Carboxylic Acids from a, b- Unsaturated Aldehydes
Winkler, Till, Enantioselective Rearrangement Coupled with Water Addition: Direct Synthesis of Enantiomerically Pure Saturated Carboxylic Acids from a, b- Unsaturated Aldehydes. ChemCatChem 6 (4). , 2014
PUB | DOI | WoS
 
[163]
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2672840
Hydroxy Functionalization of Non-Activated C-H and C=C Bonds: New Perspectives for the Synthesis of Alcohols through Biocatalytic Processes
Gröger, Harald, Hydroxy Functionalization of Non-Activated C-H and C=C Bonds: New Perspectives for the Synthesis of Alcohols through Biocatalytic Processes. Angewandte Chemie. International edition 53 (12). , 2014
PUB | DOI | WoS | PubMed | Europe PMC
 
[162]
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2621177
Direct biocatalytic one-pot-transformation of cyclohexanol with molecular oxygen into ɛ-caprolactone
Staudt, Svenja, Direct biocatalytic one-pot-transformation of cyclohexanol with molecular oxygen into ɛ-caprolactone. Enzyme and microbial technology 53 (4). , 2013
PUB | DOI | WoS | PubMed | Europe PMC
 
[161]
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2621189
Highly Enantioselective Reduction of α-Methylated Nitroalkenes
Burda, Edyta, Highly Enantioselective Reduction of α-Methylated Nitroalkenes. Angewandte Chemie (International ed. in English) 52 (35). , 2013
PUB | DOI | WoS | PubMed | Europe PMC
 
[160]
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2635953
Asymmetric Organocatalytic Aldol Reaction in Water: Mechanistic Insights and Development of a Semi-Continuously Operating Process
Rulli, Giuseppe, Asymmetric Organocatalytic Aldol Reaction in Water: Mechanistic Insights and Development of a Semi-Continuously Operating Process. Synthesis 45 (18). , 2013
PUB | DOI | WoS
 
[159]
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2637130
Towards catalyst compartimentation in combined chemo- and biocatalytic processes: Immobilization of alcohol dehydrogenases for the diastereoselective reduction of a β-hydroxy ketone obtained from an organocatalytic aldol reaction
Rulli, Giuseppe, Towards catalyst compartimentation in combined chemo- and biocatalytic processes: Immobilization of alcohol dehydrogenases for the diastereoselective reduction of a β-hydroxy ketone obtained from an organocatalytic aldol reaction. Journal of biotechnology 168 (3). , 2013
PUB | DOI | WoS | PubMed | Europe PMC
 
[158]
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2560792
Direct Oxidation of Cycloalkanes to Cycloalkanones with Oxygen in Water
Staudt, Svenja, Direct Oxidation of Cycloalkanes to Cycloalkanones with Oxygen in Water. Angewandte Chemie International Edition 52 (8). , 2013
PUB | DOI | WoS | PubMed | Europe PMC
 
[157]
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2612864
In Vitro Double Oxidation of n-Heptane with Direct Cofactor Regeneration
Mueller, Christina A., In Vitro Double Oxidation of n-Heptane with Direct Cofactor Regeneration. Advanced Synthesis & Catalysis 355 (9). , 2013
PUB | DOI | WoS
 
[156]
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2634611
Bio-integrated organic synthesis in industry: Biocatalytic breakthroughs, industrial processes, emerging fields
Gröger, Harald, Bio-integrated organic synthesis in industry: Biocatalytic breakthroughs, industrial processes, emerging fields. Journal of Biotechnology 168 (3). , 2013
PUB | DOI | WoS | PubMed | Europe PMC
 
[155]
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2647580
Development of a Continuously Operating Process for the Enantioselective Synthesis of a beta-Amino Acid Ester via a Solvent-Free Chemoenzymatic Reaction Sequence
Strompen, Simon, Development of a Continuously Operating Process for the Enantioselective Synthesis of a beta-Amino Acid Ester via a Solvent-Free Chemoenzymatic Reaction Sequence. Advanced Synthesis & Catalysis 355 (11-12). , 2013
PUB | DOI | WoS
 
[154]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2398888
Organocatalytic racemization of alpha-aryl propionates in the presence of water
Alfaro Blasco, M., Organocatalytic racemization of alpha-aryl propionates in the presence of water. Synth. Commun. 43 (1). , 2012
PUB | DOI | WoS
 
[153]
2012 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2398903
Asymmetric Biocatalytic Reduction of Ketones
Gröger, Harald, Asymmetric Biocatalytic Reduction of Ketones. Synthetic Methods VI – Enzymatic and Semi-Enzymatic 7 (). Oxford, 2012
PUB | DOI
 
[152]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2474296
Biocatalytic hydroxylation of n-butane with in situ cofactor regeneration at low temperature and under normal pressure
Staudt, Svenja, Biocatalytic hydroxylation of n-butane with in situ cofactor regeneration at low temperature and under normal pressure. Beilstein Journal of Organic Chemistry 8 (). , 2012
PUB | DOI | WoS | PubMed | Europe PMC
 
[151]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2445196
Combination of a Suzuki cross-coupling reaction using a water-soluble palladium catalyst with an asymmetric enzymatic reduction towards a one-pot reaction in aqueous medium at room temperature
Borchert, Sonja, Combination of a Suzuki cross-coupling reaction using a water-soluble palladium catalyst with an asymmetric enzymatic reduction towards a one-pot reaction in aqueous medium at room temperature. J. Mol. Catal. B: Enzym. 84 (SI). , 2012
PUB | DOI | WoS
 
[150]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2517832
Highly Enantioselective Organocatalytic Trifluoromethyl Carbinol Synthesis-A Caveat on Reaction Times and Product Isolation
Duangdee, Nongnaphat, Highly Enantioselective Organocatalytic Trifluoromethyl Carbinol Synthesis-A Caveat on Reaction Times and Product Isolation. Journal of the American Chemical Society 134 (27). , 2012
PUB | DOI | WoS | PubMed | Europe PMC
 
[149]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2553547
Efficient Enzymatic Amine Resolution at High Substrate Input Using Diethyl Malonate as an Acyl Donor of Low Hazard Potential
Simon, Sabine, Efficient Enzymatic Amine Resolution at High Substrate Input Using Diethyl Malonate as an Acyl Donor of Low Hazard Potential. Zeitschrift Fur Naturforschung Section B-A Journal Of Chemical Sciences 67b (10). , 2012
PUB | DOI | WoS
 
[148]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2474508
Large-Scale Synthesis of Singh's Catalyst in a One-Pot Procedure Starting from Proline
Berkessel, Albrecht, Large-Scale Synthesis of Singh's Catalyst in a One-Pot Procedure Starting from Proline. Organic Process Research & Development 16 (1). , 2012
PUB | DOI | WoS
 
[147]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2471821
Formal Asymmetric Hydration of Non-Activated Alkenes in Aqueous Medium through a "Chemoenzymatic Catalytic System"
Schnapperelle, Ingo, Formal Asymmetric Hydration of Non-Activated Alkenes in Aqueous Medium through a "Chemoenzymatic Catalytic System". Chemistry - A European Journal 18 (4). , 2012
PUB | DOI | WoS | PubMed | Europe PMC
 
[146]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2509926
Development of Biocatalytic Processes in Japan and Germany: From Research Synergies to Industrial Applications
Gröger, Harald, Development of Biocatalytic Processes in Japan and Germany: From Research Synergies to Industrial Applications. Chemistry - An Asian Journal 7 (6). , 2012
PUB | DOI | WoS | PubMed | Europe PMC
 
[145]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2445201
Kinetic investigation of a solvent-free, chemoenzymatic reaction sequence towards enantioselective synthesis of a ß-amino acid ester
Strompen, S., Kinetic investigation of a solvent-free, chemoenzymatic reaction sequence towards enantioselective synthesis of a ß-amino acid ester. Biotechnology and Bioengineering 109 (6). , 2012
PUB | DOI | WoS | PubMed | Europe PMC
 
[144]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2493243
Asymmetric addition of a nitrogen nucleophile to an enoate in the presence of a chiral phase-transfer catalyst: A novel approach toward enantiomerically enriched protected beta-amino acids
Weiss, Markus, Asymmetric addition of a nitrogen nucleophile to an enoate in the presence of a chiral phase-transfer catalyst: A novel approach toward enantiomerically enriched protected beta-amino acids. Heteroatom Chemistry 23 (2). , 2012
PUB | DOI | WoS
 
[143]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2490875
Synthesis of (S)-(+)-cericlamine through lipase-catalyzed aminolysis of azo acetates
Prechter, Agnes, Synthesis of (S)-(+)-cericlamine through lipase-catalyzed aminolysis of azo acetates. Organic & Biomolecular Chemistry 10 (17). , 2012
PUB | DOI | WoS | PubMed | Europe PMC
 
[142]
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344704
Combination of C=C Bond Formation by Wittig Reaction and Enzymatic C=C Bond Reduction in a One-Pot Process in Water
Krausser, Marina, Combination of C=C Bond Formation by Wittig Reaction and Enzymatic C=C Bond Reduction in a One-Pot Process in Water. CHEMCATCHEM 3 (2). , 2011
PUB | DOI | WoS
 
[141]
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344730
Asymmetric reduction of activated alkenes using an enoate reductase from Gluconobacter oxydans
Richter, Nina, Asymmetric reduction of activated alkenes using an enoate reductase from Gluconobacter oxydans. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY 89 (1). , 2011
PUB | DOI | WoS | PubMed | Europe PMC
 
[140]
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2398890
Combination of Olefin Metathesis and Enzymatic Ester Hydrolysis in Aqueous Media in a One-Pot Synthesis
Tenbrink, Katharina, Combination of Olefin Metathesis and Enzymatic Ester Hydrolysis in Aqueous Media in a One-Pot Synthesis. Adv. Synth. & Catal. 353 (13). , 2011
PUB | DOI | WoS
 
[139]
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2407538
Eisenkatalyse zur In-situ-Regenerierung oxidierter Cofaktoren durch Aktivierung und Reduktion von O2: ein synthetisches Metallporphyrin als biomimetische NAD(P)H-Oxidase
Maid, H., Eisenkatalyse zur In-situ-Regenerierung oxidierter Cofaktoren durch Aktivierung und Reduktion von O2: ein synthetisches Metallporphyrin als biomimetische NAD(P)H-Oxidase. Angew. Chem. 123 (10). , 2011
PUB | DOI | WoS | PubMed | Europe PMC
 
[138]
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2407610
Gesteuerte kinetisch oder thermodynamisch kontrollierte Organokatalyse und Anwendung in der chemoenzymatischen Synthese
Rulli, Giuseppe, Gesteuerte kinetisch oder thermodynamisch kontrollierte Organokatalyse und Anwendung in der chemoenzymatischen Synthese. Angew. Chem. 123 (34). , 2011
PUB | DOI
 
[137]
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344701
ChemCatChem: Cluster Issue on Chemoenzymatic Synthesis
Gröger, Harald, ChemCatChem: Cluster Issue on Chemoenzymatic Synthesis. CHEMCATCHEM 3 (2). , 2011
PUB | DOI | WoS
 
[136]
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344713
Direction of Kinetically versus Thermodynamically Controlled Organocatalysis and Its Application in Chemoenzymatic Synthesis
Rulli, Giuseppe, Direction of Kinetically versus Thermodynamically Controlled Organocatalysis and Its Application in Chemoenzymatic Synthesis. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 50 (34). , 2011
PUB | DOI | WoS | PubMed | Europe PMC
 
[135]
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344695
Chiral azo compounds: enantioselective synthesis and transformations into beta-amino alcohols and alpha-amino acids with a quaternary stereocenter
Dietz, Friedrich R., Chiral azo compounds: enantioselective synthesis and transformations into beta-amino alcohols and alpha-amino acids with a quaternary stereocenter. TETRAHEDRON LETTERS 52 (6). , 2011
PUB | DOI | WoS
 
[134]
2011 | Sammelwerksbeitrag | Im Druck | PUB-ID: 2397699
Reduction of Ketones and Aldehydes to Alcohols
Gröger, Harald, Reduction of Ketones and Aldehydes to Alcohols. Enzyme Catalysis in Organic Synthesis Chapter 12.1 (). Weinheim, 2011
PUB
 
[133]
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344721
Iron Catalysis for In Situ Regeneration of Oxidized Cofactors by Activation and Reduction of Molecular Oxygen: A Synthetic Metalloporphyrin as a Biomimetic NAD(P)H Oxidase
Maid, Harald, Iron Catalysis for In Situ Regeneration of Oxidized Cofactors by Activation and Reduction of Molecular Oxygen: A Synthetic Metalloporphyrin as a Biomimetic NAD(P)H Oxidase. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 50 (10). , 2011
PUB | DOI | WoS | PubMed | Europe PMC
 
[132]
2011 | Sammelwerksbeitrag | Im Druck | PUB-ID: 2397744
Hydrolysis and Formation of Carboxylic Acid Esters
Paravidino, M., Hydrolysis and Formation of Carboxylic Acid Esters. Enzyme Catalysis in Organic Synthesis Cahpter 8.1 (). Weinheim, 2011
PUB
 
[131]
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2394651
A study towards efficient L-threonine aldolase-catalyzed enantio- and diastereoselective aldol reactions of glycine with substituted benzaldehydes: biocatalyst production and process development
Baer, Katrin, A study towards efficient L-threonine aldolase-catalyzed enantio- and diastereoselective aldol reactions of glycine with substituted benzaldehydes: biocatalyst production and process development. Tetrahedron Asymmetry 22 (9). , 2011
PUB | DOI | WoS
 
[130]
2011 | Patent | PUB-ID: 2453495
Enzymreaktionen in Miniemulsionen
Gröger, Harald, Enzymreaktionen in Miniemulsionen. (). , 2011
PUB
 
[129]
2011 | Sammelwerksbeitrag | Im Druck | PUB-ID: 2397781
Reductive Amination of alpha-Keto Acids
Hummel, W., Reductive Amination of alpha-Keto Acids. Enzyme Catalysis in Organic Synthesis Chapter 12.3 (). Weinheim, 2011
PUB
 
[128]
2011 | Patent | Veröffentlicht | PUB-ID: 2458477
Verfahren zur Herstellung von enantiomerenangereicherten Azoverbindungen, Aminoalkoholen und Aminosäuren mit einem quartären Kohlenstoffzentrum
Heinrich, M., Verfahren zur Herstellung von enantiomerenangereicherten Azoverbindungen, Aminoalkoholen und Aminosäuren mit einem quartären Kohlenstoffzentrum. (). , 2011
PUB
 
[127]
2011 | Zeitschriftenaufsatz | Im Druck | PUB-ID: 2445179
Formal Enantioselective Hydratation of Alkenes: Combination of Wacker-Oxidation and Biocatalytic Reduction in a One-Pot Process in Aqueous Media
Schnapperelle, I., Formal Enantioselective Hydratation of Alkenes: Combination of Wacker-Oxidation and Biocatalytic Reduction in a One-Pot Process in Aqueous Media. Chem. Eur. J. (). , 2011
PUB
 
[126]
2011 | Sammelwerksbeitrag | Im Druck | PUB-ID: 2445173
Introduction - Milestones of the Development of Enzyme Catalysis in Organic Synthesis
Gröger, Harald, Introduction - Milestones of the Development of Enzyme Catalysis in Organic Synthesis. Enzyme Catalysis in Organic Synthesis (). Weinheim, 2011
PUB
 
[125]
2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344754
Enantioselective biocatalytic synthesis of (S)-monastrol
Alfaro Blasco, Maria, Enantioselective biocatalytic synthesis of (S)-monastrol. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS 20 (15). , 2010
PUB | DOI | WoS | PubMed | Europe PMC
 
[124]
2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344761
Expanding the Application Range of Aldolases: Novel Asymmetric Syntheses of alpha-Methylated beta-Hydroxy alpha-Amino Acids and beta-Amino Alcohols
Baer, Katrin, Expanding the Application Range of Aldolases: Novel Asymmetric Syntheses of alpha-Methylated beta-Hydroxy alpha-Amino Acids and beta-Amino Alcohols. CHEMCATCHEM 2 (8). , 2010
PUB | DOI | WoS
 
[123]
2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344778
Enantio- and Diastereoselective Chemoenzymatic Synthesis of C2-Symmetric Biaryl-Containing Diols
Burda, Edyta, Enantio- and Diastereoselective Chemoenzymatic Synthesis of C2-Symmetric Biaryl-Containing Diols. CHEMCATCHEM 2 (1). , 2010
PUB | DOI | WoS
 
[122]
2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344737
Threonine aldolases-screening, properties and applications in the synthesis of non-proteinogenic beta-hydroxy-alpha-amino acids
Dückers, Nina, Threonine aldolases-screening, properties and applications in the synthesis of non-proteinogenic beta-hydroxy-alpha-amino acids. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY 88 (2). , 2010
PUB | DOI | WoS | PubMed | Europe PMC
 
[121]
2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344744
Highly conserved progesterone 5 beta-reductase genes (P5 beta R) from 5 beta-cardenolide-free and 5 beta-cardenolide-producing angiosperms
Bauer, Peter, Highly conserved progesterone 5 beta-reductase genes (P5 beta R) from 5 beta-cardenolide-free and 5 beta-cardenolide-producing angiosperms. PHYTOCHEMISTRY 71 (13). , 2010
PUB | DOI | WoS | PubMed | Europe PMC
 
[120]
2010 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2344784
Regeneration of Nicotinamide Coenzymes: Principles and Applications for the Synthesis of Chiral Compounds
Weckbecker, Andrea, Regeneration of Nicotinamide Coenzymes: Principles and Applications for the Synthesis of Chiral Compounds. BIOSYSTEMS ENGINEERING I: CREATING SUPERIOR BIOCATALYSTS 120 (). , 2010
PUB | DOI | WoS | PubMed | Europe PMC
 
[119]
2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344772
Enantioselective Biocatalytic Reduction of Non-protected Hydroxyacetophenones
Neupert, Adrian, Enantioselective Biocatalytic Reduction of Non-protected Hydroxyacetophenones. Zeitschrift für Naturforschung. Section B, a journal of chemical sciences 65 (3). , 2010
PUB | DOI | WoS
 
[118]
2010 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2396569
Enzyme-Catalyzed Asymmetric Synthesis
Gröger, Harald, Enzyme-Catalyzed Asymmetric Synthesis. Catalytic Asymmetric Synthesis 6 (). Hoboken, New Jersey, 2010
PUB
 
[117]
2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344790
Towards a greener synthesis of (S)-3-aminobutanoic acid: process development and environmental assessment
Weiss, Markus, Towards a greener synthesis of (S)-3-aminobutanoic acid: process development and environmental assessment. GREEN CHEMISTRY 12 (9). , 2010
PUB | DOI | WoS
 
[116]
2010 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2396563
Enzyme-Catalyzed Asymmetric Reduction of Ketones
Gröger, Harald, Enzyme-Catalyzed Asymmetric Reduction of Ketones. Encyclopedia of Industrial Biotechnology, Bioprocess, Bioseparation, and Cell Technology 3 (). New York, 2010
PUB
 
[115]
2010 | Patent | PUB-ID: 2453130
Verfahren zur Herstellung von optisch aktiven Aminosäuren mittels eines Ganzzellkatalysators
Altenbuchner, J., Verfahren zur Herstellung von optisch aktiven Aminosäuren mittels eines Ganzzellkatalysators. (). , 2010
PUB
 
[114]
2010 | Patent | PUB-ID: 2453301
Verfahren zur enzymatischen Umsetzung von Alkanen
Gröger, Harald, Verfahren zur enzymatischen Umsetzung von Alkanen. (). , 2010
PUB
 
[113]
2010 | Patent | Veröffentlicht | PUB-ID: 2399883
Verfahren zur Herstellung von überwiegend ein Enantiomer enthaltendem 1,1,1-Trifluorpropanol
Doderer, K., Verfahren zur Herstellung von überwiegend ein Enantiomer enthaltendem 1,1,1-Trifluorpropanol. (). , 2010
PUB
 
[112]
2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344767
Purification, cloning, and overexpression of an alcohol dehydrogenase from Nocardia globerula reducing aliphatic ketones and bulky ketoesters
Parkot, Julia, Purification, cloning, and overexpression of an alcohol dehydrogenase from Nocardia globerula reducing aliphatic ketones and bulky ketoesters. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY 86 (6). , 2010
PUB | DOI | WoS | PubMed | Europe PMC
 
[111]
2010 | Patent | PUB-ID: 2453169
Herstellung optisch aktiver Alkohole mit Hilfe von Ganzzellkatalsatoren
Gröger, Harald, Herstellung optisch aktiver Alkohole mit Hilfe von Ganzzellkatalsatoren. (). , 2010
PUB
 
[110]
2009 | Patent | PUB-ID: 2453000
ADH aus Rhodococcus erythropolis
Hummel, W., ADH aus Rhodococcus erythropolis. (). , 2009
PUB
 
[109]
2009 | Patent | PUB-ID: 2453012
Verfahren zur enzymatischen Herstellung enantiomerenangereicherter ß-Aminosäuren
Gröger, Harald, Verfahren zur enzymatischen Herstellung enantiomerenangereicherter ß-Aminosäuren. (). , 2009
PUB
 
[108]
2009 | Patent | PUB-ID: 2453151
Neue Alkoholdehydrogenasen
Schulze, R., Neue Alkoholdehydrogenasen. (). , 2009
PUB
 
[107]
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344799
Recombinant Delta(4,5)-Steroid 5 beta-Reductases as Biocatalysts for the Reduction of Activated C=C-Double Bonds in Monocyclic and Acyclic Molecules
Burda, Edyta, Recombinant Delta(4,5)-Steroid 5 beta-Reductases as Biocatalysts for the Reduction of Activated C=C-Double Bonds in Monocyclic and Acyclic Molecules. ADVANCED SYNTHESIS & CATALYSIS 351 (17). , 2009
PUB | DOI | WoS
 
[106]
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344823
Sequential and Modular Synthesis of Chiral 1,3-Diols with Two Stereogenic Centers: Access to All Four Stereoisomers by Combination of Organo- and Biocatalysis
Baer, Katrin, Sequential and Modular Synthesis of Chiral 1,3-Diols with Two Stereogenic Centers: Access to All Four Stereoisomers by Combination of Organo- and Biocatalysis. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 48 (49). , 2009
PUB | DOI | WoS | PubMed | Europe PMC
 
[105]
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2346641
Multistep one-pot processes in aqueous media by combination of palladium-catalyzed cross-coupling reactions and biotransformations
Burda, Edyta, Multistep one-pot processes in aqueous media by combination of palladium-catalyzed cross-coupling reactions and biotransformations. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY 238 (). , 2009
PUB | WoS
 
[104]
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344795
Asymmetric Synthesis of All Stereoisomers of alpha-Methylthreonine Using an Organocatalytic Steglich Rearrangement Reaction as a Key Step
Dietz, Friedrich R., Asymmetric Synthesis of All Stereoisomers of alpha-Methylthreonine Using an Organocatalytic Steglich Rearrangement Reaction as a Key Step. SYNTHESIS-STUTTGART (24). , 2009
PUB | DOI | WoS
 
[103]
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2346645
Practical, Highly Enantioselective Chemoenzymatic One-Pot Synthesis of Short-Chain Aliphatic beta-Amino Acid Esters
Weiss, Markus, Practical, Highly Enantioselective Chemoenzymatic One-Pot Synthesis of Short-Chain Aliphatic beta-Amino Acid Esters. SYNLETT 2009 (08). , 2009
PUB | DOI | WoS
 
[102]
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2407531
Sequenzielle und modulare Synthese von chiralen 1,3-Diolen mit zwei Stereozentren: Zugang zu allen vier Stereoisomeren durch Kombination von Organo- und Biokatalyse
Baer, K., Sequenzielle und modulare Synthese von chiralen 1,3-Diolen mit zwei Stereozentren: Zugang zu allen vier Stereoisomeren durch Kombination von Organo- und Biokatalyse. Angew. Chem. 121 (49). , 2009
PUB | DOI
 
[101]
2009 | Patent | PUB-ID: 2453286
Verfahren zur Herstellung von enantimerenangereicherten Aminen
Doderer, K., Verfahren zur Herstellung von enantimerenangereicherten Aminen. (). , 2009
PUB
 
[100]
2009 | Patent | Veröffentlicht | PUB-ID: 2400139
Aufarbeitung von Reaktionslösungen aus Ganzzell-Biotransformationen
Gröger, Harald, Aufarbeitung von Reaktionslösungen aus Ganzzell-Biotransformationen. (). , 2009
PUB
 
[99]
2009 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2396636
Biocatalytic Synthesis of Natural and Non-Natural alpha-Amino Acids
Gröger, Harald, Biocatalytic Synthesis of Natural and Non-Natural alpha-Amino Acids. Wiley Encyclopedia of Chemical Biology 1 (). Hoboken, 2009
PUB
 
[98]
2009 | Patent | PUB-ID: 2453051
Gekoppeltes cofaktorabhängiges enzymatisches Reaktionssystem
Gröger, Harald, Gekoppeltes cofaktorabhängiges enzymatisches Reaktionssystem. (). , 2009
PUB
 
[97]
2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344831
Novel catalytic synthetic route to protected alpha-methyl threonine and the first asymmetric acetyl migration in a Steglich rearrangement reaction
Dietz, Friedrich R., Novel catalytic synthetic route to protected alpha-methyl threonine and the first asymmetric acetyl migration in a Steglich rearrangement reaction. SYNLETT 2008 (5). , 2008
PUB | DOI | WoS
 
[96]
2008 | Konferenzbeitrag | Veröffentlicht | PUB-ID: 2347145
Asymmetric organocatalysis on a technical scale: current status and future challenges
Gröger, Harald, Asymmetric organocatalysis on a technical scale: current status and future challenges. Organocatalysis (). Berlin u.a., 2008
PUB | DOI | PubMed | Europe PMC
 
[95]
2008 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2396697
Asymmetric Organocatalysis on a Technical Scale: Current Status and Future Challenges
Gröger, Harald, Asymmetric Organocatalysis on a Technical Scale: Current Status and Future Challenges. Ernst Schering Foundation Symposium Proceedings 2007-2: Organocatalysis (). Berlin, Heidelberg, 2008
PUB | DOI
 
[94]
2008 | Patent | PUB-ID: 2453245
Verfahren zur Herstellung von enantiomerenangereicherten Alkylencarbonaten
Gröger, Harald, Verfahren zur Herstellung von enantiomerenangereicherten Alkylencarbonaten. (). , 2008
PUB
 
[93]
2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344840
Enantioselective C-C bond ligation using recombinant Escherichia coli-whole-cell biocatalysts
Dominguez de Maria, Pablo, Enantioselective C-C bond ligation using recombinant Escherichia coli-whole-cell biocatalysts. ADVANCED SYNTHESIS & CATALYSIS 350 (1). , 2008
PUB | DOI | WoS
 
[92]
2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344835
Modular Chemoenzymatic One-Pot Syntheses in Aqueous Media: Combination of a Palladium-Catalyzed Cross-Coupling with an Asymmetric Biotransformation
Burda, Edyta, Modular Chemoenzymatic One-Pot Syntheses in Aqueous Media: Combination of a Palladium-Catalyzed Cross-Coupling with an Asymmetric Biotransformation. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 47 (49). , 2008
PUB | DOI | WoS | PubMed | Europe PMC
 
[91]
2008 | Patent | PUB-ID: 2453216
Verfahren zur Herstellung von enantiomerenangereicherten Aminen und Amiden durch enzymatische Racematspaltung
Gröger, Harald, Verfahren zur Herstellung von enantiomerenangereicherten Aminen und Amiden durch enzymatische Racematspaltung. (). , 2008
PUB
 
[90]
2008 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2396674
Chiral Trivalent Phosphorus Compounds as Organocatalysts in Asymmetric Synthesis
Gröger, Harald, Chiral Trivalent Phosphorus Compounds as Organocatalysts in Asymmetric Synthesis. Phosphorous Ligands in Asymmetric Catalysis - Synthesis and Applications 3 (). Weinheim, 2008
PUB
 
[89]
2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2407518
Modulare chemoenzymatische Eintopfsynthesen im wässrigen Medium: Kombination einer Palladium-katalysierten Kreuzkupplung mit einer asymmetrischen Biotransformation
Burda, E., Modulare chemoenzymatische Eintopfsynthesen im wässrigen Medium: Kombination einer Palladium-katalysierten Kreuzkupplung mit einer asymmetrischen Biotransformation. Angew. Chem. 120 (49). , 2008
PUB | DOI
 
[88]
2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2346666
Practical two-step synthesis of an enantiopure aliphatic terminal (S)-epoxide based on reduction of haloalkanones with ``Designer Cells''
Berkessel, Albrecht, Practical two-step synthesis of an enantiopure aliphatic terminal (S)-epoxide based on reduction of haloalkanones with ``Designer Cells''. ADVANCED SYNTHESIS & CATALYSIS 349 (17-18). , 2007
PUB | DOI | WoS
 
[87]
2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2346685
Enantioselective reduction of 4-fluoroacetophenone at high substrate concentration using a tailor-made recombinant whole-cell catalyst
Gröger, Harald, Enantioselective reduction of 4-fluoroacetophenone at high substrate concentration using a tailor-made recombinant whole-cell catalyst. ADVANCED SYNTHESIS & CATALYSIS 349 (4-5). , 2007
PUB | DOI | WoS
 
[86]
2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344854
Alcohol dehydrogenase whole-cell catalysts - A broad technology platform for life science applications
Osswald, S., Alcohol dehydrogenase whole-cell catalysts - A broad technology platform for life science applications. CHIMICA OGGI-CHEMISTRY TODAY 25 (5, S). , 2007
PUB
 
[85]
2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344865
Asymmetric synthesis of aliphatic 2-hydroxy ketones by enzymatic carboligation of aldehydes
Dominguez de Maria, Pablo, Asymmetric synthesis of aliphatic 2-hydroxy ketones by enzymatic carboligation of aldehydes. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY 2007 (18). , 2007
PUB | DOI | WoS
 
[84]
2007 | Patent | PUB-ID: 2453180
Verfahren zur Herstellung primärer Alkohole
Gröger, Harald, Verfahren zur Herstellung primärer Alkohole. (). , 2007
PUB
 
[83]
2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2346674
Enantioselective one-pot two-step synthesis of hydrophobic allylic alcohols in aqueous medium through the combination of a wittig reaction and an enzymatic ketone reduction
Krausser, Marina, Enantioselective one-pot two-step synthesis of hydrophobic allylic alcohols in aqueous medium through the combination of a wittig reaction and an enzymatic ketone reduction. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY 2007 (31). , 2007
PUB | DOI | WoS
 
[82]
2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2346679
Biocatalytic alclehyde reduction using tailor-made whole-cell catalysts: a novel synthesis of the aroma chemical cinnamyl alcohol
Chamouleau, Francoise, Biocatalytic alclehyde reduction using tailor-made whole-cell catalysts: a novel synthesis of the aroma chemical cinnamyl alcohol. FLAVOUR AND FRAGRANCE JOURNAL 22 (3). , 2007
PUB | DOI | WoS
 
[81]
2007 | Patent | PUB-ID: 2399880
Alkoholdehydrogenase aus Nocardia globulera und deren Verwendung
Hummel, W., Alkoholdehydrogenase aus Nocardia globulera und deren Verwendung. (). , 2007
PUB
 
[80]
2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2396781
Enantioselektive Enzymreaktionen in Miniemulsionen als effiziente "Nanoreaktoren"
Gröger, Harald, Enantioselektive Enzymreaktionen in Miniemulsionen als effiziente "Nanoreaktoren". Angew. Chem. Int. Ed. (45). , 2006
PUB
 
[79]
2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2407494
Enantioselektive Ketonreduktion mit "Designerzellen" bei hohen Substratkonzentrationen: Hocheffizienter Zugang zu funktionalisierten optisch aktiven Alkoholen
Gröger, Harald, Enantioselektive Ketonreduktion mit "Designerzellen" bei hohen Substratkonzentrationen: Hocheffizienter Zugang zu funktionalisierten optisch aktiven Alkoholen. Angew. Chem. 118 (34). , 2006
PUB | DOI
 
[78]
2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347147
Enantioselective reduction of ketones with "designer cells" at high substrate concentrations: highly efficient access to functionalized optically active alcohols
Gröger, Harald, Enantioselective reduction of ketones with "designer cells" at high substrate concentrations: highly efficient access to functionalized optically active alcohols. Angewandte Chemie International Edition 45 (34). , 2006
PUB | DOI | WoS | PubMed | Europe PMC
 
[77]
2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2396830
Preparative Enantioselective Synthesis of Benzoins and (R)-2-Hydroxy-1-phenyl-propanone Using Benzaldehyde Lyase
Dominguez de Maria, P., Preparative Enantioselective Synthesis of Benzoins and (R)-2-Hydroxy-1-phenyl-propanone Using Benzaldehyde Lyase. J. Mol. Catal. B: Enzym. 38 (1). , 2006
PUB | DOI | WoS
 
[76]
2006 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2396733
Biocatalytic Concepts for the Synthesis of Optically Active Amines
Buchholz, S., Biocatalytic Concepts for the Synthesis of Optically Active Amines. Biocatalysis in the Pharmaceutical and Biotechnology Industries (). New York, 2006
PUB
 
[75]
2006 | Patent | PUB-ID: 2399875
Verfahren zur Herstellung von enantiomer angereicherten alpha-Hydroxyketonen
Dominguez de Maria, P., Verfahren zur Herstellung von enantiomer angereicherten alpha-Hydroxyketonen. (). , 2006
PUB
 
[74]
2006 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2396749
Enationselective Biocatalytic Reduction of Ketones for the Synthesis of Optically Active Alcohols
Buchholz, S., Enationselective Biocatalytic Reduction of Ketones for the Synthesis of Optically Active Alcohols. Biocatalysis in the Pharmaceutical and Biotechnology Industries Chapter 32 (). New York, 2006
PUB
 
[73]
2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2396819
A "Second Generation-Process" for the Synthesis of L-Neopentylglycine: Asymmetric Reductive Amination Using a Recombinant Whole Cell Catalyst
Gröger, Harald, A "Second Generation-Process" for the Synthesis of L-Neopentylglycine: Asymmetric Reductive Amination Using a Recombinant Whole Cell Catalyst. Org. Proc. Res. Developm. 10 (3). , 2006
PUB | DOI | WoS
 
[72]
2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2407476
Enantioselektive Enzymreaktionen in Miniemulsionen als effiziente "Nanoreaktoren"
Gröger, Harald, Enantioselektive Enzymreaktionen in Miniemulsionen als effiziente "Nanoreaktoren". Angew. Chem. (118). , 2006
PUB
 
[71]
2005 | Patent | PUB-ID: 2399843
Enzymatische Reaktionen in Gegenwart ionischer Additive
Wallert, S., Enzymatische Reaktionen in Gegenwart ionischer Additive. (). , 2005
PUB
 
[70]
2005 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2396902
Ganzzellbiokatalyse
Buchholz, S., Ganzzellbiokatalyse. Angewandte Mikrobiologie Chapter 8 (). Heidelberg, 2005
PUB
 
[69]
2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2396930
Improved Process for the Enantioselective Hydrolysis of Prochiral Diethyl Malonates Catalyzed by Pig Liver Esterase
Dominguez de Maria, P., Improved Process for the Enantioselective Hydrolysis of Prochiral Diethyl Malonates Catalyzed by Pig Liver Esterase. Synlett (11). , 2005
PUB | DOI | WoS
 
[68]
2005 | Monographie | Veröffentlicht | PUB-ID: 2397104
Asymmetric Organocatalysis
Berkessel, A., Asymmetric Organocatalysis. (). Weinheim, 2005
PUB | DOI
 
[67]
2005 | Patent | PUB-ID: 2399762
Verfahren zur Herstellung von D-Aminosäuren
Hummel, H., Verfahren zur Herstellung von D-Aminosäuren. (). , 2005
PUB
 
[66]
2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2396908
Ionic liquids as Additives in the Pig Liver Esterase (PLE) Catalyzed Synthesis of Chiral Disubstituted Malonates
Wallert, S., Ionic liquids as Additives in the Pig Liver Esterase (PLE) Catalyzed Synthesis of Chiral Disubstituted Malonates. Green Chem. 7 (8). , 2005
PUB | DOI | WoS
 
[65]
2004 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347164
The first aminoacylase-catalyzed enantioselective synthesis of aromatic beta-amino acids
Gröger, Harald, The first aminoacylase-catalyzed enantioselective synthesis of aromatic beta-amino acids. Org. Biomol. Chemistry 2 (14). , 2004
PUB | DOI | WoS | PubMed | Europe PMC
 
[64]
2004 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397106
From Enzymes to "Designer Bugs" in Reductive Amination: A New Process for the Synthesis of L-tert-Leucine Using a Whole Cell-Catalyst
Menzel, A., From Enzymes to "Designer Bugs" in Reductive Amination: A New Process for the Synthesis of L-tert-Leucine Using a Whole Cell-Catalyst. Eng. Life Sciences 4 (). , 2004
PUB
 
[63]
2004 | Patent | PUB-ID: 2399668
Gekoppeltes enzymatisches Reaktionssystem
Gröger, Harald, Gekoppeltes enzymatisches Reaktionssystem. (). , 2004
PUB
 
[62]
2004 | Patent | PUB-ID: 2399670
Gekoppeltes enzymatisches Reaktionssystem unter Einsatz einer Formiatdehydrogenase aus Candida boidinii
Gröger, Harald, Gekoppeltes enzymatisches Reaktionssystem unter Einsatz einer Formiatdehydrogenase aus Candida boidinii. (). , 2004
PUB
 
[61]
2004 | Patent | PUB-ID: 2399682
Enzymatisches Reaktionssystem
Hummel, W., Enzymatisches Reaktionssystem. (). , 2004
PUB
 
[60]
2004 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397117
Preparative Asymmetric Reduction of Ketones in a Biphasic Medium with an (S)-AIcohol Dehydrogenase under in situ-Cofactor-Recycling with a Formate Dehydrogenase
Gröger, Harald, Preparative Asymmetric Reduction of Ketones in a Biphasic Medium with an (S)-AIcohol Dehydrogenase under in situ-Cofactor-Recycling with a Formate Dehydrogenase. Tetrahedron 60 (3). , 2004
PUB | DOI | WoS
 
[59]
2004 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2397155
Nitroaldol Reaction
Shibasaki, M., Nitroaldol Reaction. Comprehensive Asymmetric Catalysis, Supplement 1 (). Heidelberg, 2004
PUB
 
[58]
2004 | Patent | PUB-ID: 2399679
Verwendung von Malatdehydrogenase zur NADH-Regenerierung
Naamniek, S., Verwendung von Malatdehydrogenase zur NADH-Regenerierung. (). , 2004
PUB
 
[57]
2004 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397147
Enzymatic Cofactor-Regeneration Technology Platforms for Chiral alpha-Amino Acids and Alcohols
May, O., Enzymatic Cofactor-Regeneration Technology Platforms for Chiral alpha-Amino Acids and Alcohols. Speciality Chemicals Magazine 5 (). , 2004
PUB
 
[56]
2004 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2397178
Methods for the Biocatalytic Production of L-Amino Acids on Industrial Scale
Gröger, Harald, Methods for the Biocatalytic Production of L-Amino Acids on Industrial Scale. Large-Scale Asymmetric Catalysis (). Weinheim, 2004
PUB
 
[55]
2004 | Patent | PUB-ID: 2399703
Gekoppeltes cofaktorabhängiges enzymatisches Reaktionssystem
Rollmann, C., Gekoppeltes cofaktorabhängiges enzymatisches Reaktionssystem. (). , 2004
PUB
 
[54]
2003 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347176
Practical asymmetric enzymatic reduction through discovery of a dehydrogenase-compatible biphasic reaction media
Gröger, Harald, Practical asymmetric enzymatic reduction through discovery of a dehydrogenase-compatible biphasic reaction media. Organic Letters 5 (2). , 2003
PUB | DOI | WoS | PubMed | Europe PMC
 
[53]
2003 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347173
Catalytic enantioselective Strecker reactions and analogous syntheses
Gröger, Harald, Catalytic enantioselective Strecker reactions and analogous syntheses. Chemical Reviews 103 (8). , 2003
PUB | DOI | WoS | PubMed | Europe PMC
 
[52]
2003 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397219
Towards a Large-Scale Asymmetric Reduction Process with Isolated Enzymes: Expression of an (S)-Alcohol Dehydrogenase in E. coli and Studies on the Synthetic Potential of this Biocatalyst
Hummel, W., Towards a Large-Scale Asymmetric Reduction Process with Isolated Enzymes: Expression of an (S)-Alcohol Dehydrogenase in E. coli and Studies on the Synthetic Potential of this Biocatalyst. Adv. Synth. Catal. 345 (). , 2003
PUB
 
[51]
2003 | Patent | PUB-ID: 2399663
Verfahren zur enzymatischen Herstellung enantiomerenangereicherter ß-Aminosäuren
Gröger, Harald, Verfahren zur enzymatischen Herstellung enantiomerenangereicherter ß-Aminosäuren. (). , 2003
PUB
 
[50]
2003 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2397232
Simple Amino acids and Short-chain Peptides as Efficient Metal-free Catalysts in Asymmetric Synthesis
Gröger, Harald, Simple Amino acids and Short-chain Peptides as Efficient Metal-free Catalysts in Asymmetric Synthesis. Organic Synthesis Highlights (). Weinheim, 2003
PUB
 
[49]
2003 | Patent | PUB-ID: 2399205
Verfahren zur Kristallisation von Oxonorleucinacetal
Schwarm, M., Verfahren zur Kristallisation von Oxonorleucinacetal. (). , 2003
PUB
 
[48]
2003 | Patent | PUB-ID: 2399215
Verfahren zur Herstellung von optisch aktiven ß-Aminocarbonsäuren aus racemischen N-acetylierten ß-Aminocarbonsäuren
Gröger, Harald, Verfahren zur Herstellung von optisch aktiven ß-Aminocarbonsäuren aus racemischen N-acetylierten ß-Aminocarbonsäuren. (). , 2003
PUB
 
[47]
2002 | Patent | PUB-ID: 2399141
Verfahren zur Herstellung von Amiden
Sans, J., Verfahren zur Herstellung von Amiden. (). , 2002
PUB
 
[46]
2002 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397245
Biocatalytic Asymmetric Hydrocyanation in the Presence of (R)-Oxynitrilases Entrapped in Lens-Shaped Gels
Gröger, Harald, Biocatalytic Asymmetric Hydrocyanation in the Presence of (R)-Oxynitrilases Entrapped in Lens-Shaped Gels. Landbauforschung Völkenrode Sonderheft (Special Issue) 241 (). , 2002
PUB
 
[45]
2002 | Patent | PUB-ID: 2399100
Verfahren zur Herstellung von N-Phosphonomethyliminodiessigsäure
Gröger, Harald, Verfahren zur Herstellung von N-Phosphonomethyliminodiessigsäure. (). , 2002
PUB
 
[44]
2002 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2397254
Special Catalysts and Processes: Biocatalysis and Enzyme-Analogous Processes
Schultz, C., Special Catalysts and Processes: Biocatalysis and Enzyme-Analogous Processes. Applied Homogeneous Catalysis with Organometallic Compounds 2 (). Weinheim, 2002
PUB
 
[43]
2002 | Patent | PUB-ID: 2399176
Verfahren zur Herstellung von optisch aktiven Cyanhydrinen
Shibasaki, M., Verfahren zur Herstellung von optisch aktiven Cyanhydrinen. (). , 2002
PUB
 
[42]
2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397265
The Development of New Monometallic Bifunctional Catalysts with Lewis Acid and Lewis Base properties, and their Applicationin Asymmetric Cyanation Reactions
Gröger, Harald, The Development of New Monometallic Bifunctional Catalysts with Lewis Acid and Lewis Base properties, and their Applicationin Asymmetric Cyanation Reactions. Chem. Eur. J. 7 (). , 2001
PUB
 
[41]
2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347186
The development of new monometallic bifunctional catalysts with Lewis acid and Lewis base properties, and their application in asymmetric cyanation reactions
Gröger, Harald, The development of new monometallic bifunctional catalysts with Lewis acid and Lewis base properties, and their application in asymmetric cyanation reactions. Chemistry 7 (24). , 2001
PUB | DOI | PubMed | Europe PMC
 
[40]
2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397268
Enzymatic Routes to Enantiomerically Pure Aromatic alpha-Hydroxy Carboxylic Acids: A Further Example for the Diversity of Biocatalysis
Gröger, Harald, Enzymatic Routes to Enantiomerically Pure Aromatic alpha-Hydroxy Carboxylic Acids: A Further Example for the Diversity of Biocatalysis. Adv. Synth. Catal. 343 (). , 2001
PUB
 
[39]
2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397279
The Application of L-Proline as an Enzyme Mimic and Further New Asymmetric Syntheses Using Small Organic Molecules as Chiral Catalysis
Gröger, Harald, The Application of L-Proline as an Enzyme Mimic and Further New Asymmetric Syntheses Using Small Organic Molecules as Chiral Catalysis. Angew. Chem. Int. Ed. 40 (). , 2001
PUB
 
[38]
2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347191
Asymmetric synthesis of an (R)-cyanohydrin using enzymes entrapped in lens-shaped gels
Gröger, Harald, Asymmetric synthesis of an (R)-cyanohydrin using enzymes entrapped in lens-shaped gels. Organic Letters 3 (13). , 2001
PUB | DOI | WoS | PubMed | Europe PMC
 
[37]
2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397285
Anti- and Syn-Selective Cyanosilylation Reactions Promoted by a Sugar-Based Bifunctional Catalyst: Stereoselective Synthesis of Essential building Blocks for HIV Protease Inhibitors and Bestatin
Manickam, G., Anti- and Syn-Selective Cyanosilylation Reactions Promoted by a Sugar-Based Bifunctional Catalyst: Stereoselective Synthesis of Essential building Blocks for HIV Protease Inhibitors and Bestatin. Synlett (). , 2001
PUB
 
[36]
2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2407474
Die Anwendung von L-Prolin als Enzymmimetikum und weitere neue asymmetrische Synthesen mit kleinen organischen Molekülen als chiralen Katalysatoren
Gröger, Harald, Die Anwendung von L-Prolin als Enzymmimetikum und weitere neue asymmetrische Synthesen mit kleinen organischen Molekülen als chiralen Katalysatoren. Angewandte Chem. (113). , 2001
PUB
 
[35]
2001 | Patent | PUB-ID: 2399121
Method for Producing Optically Active Cyanohydrins
Gröger, Harald, Method for Producing Optically Active Cyanohydrins. (). , 2001
PUB
 
[34]
2001 | Patent | PUB-ID: 2399126
Verfahren zur Herstellung von Amiden oder Estern
Gröger, Harald, Verfahren zur Herstellung von Amiden oder Estern. (). , 2001
PUB
 
[33]
2000 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347215
Catalytic concepts for the enantioselective synthesis of alpha-amino and alpha-hydroxy phosphonates
Gröger, Harald, Catalytic concepts for the enantioselective synthesis of alpha-amino and alpha-hydroxy phosphonates. Chemistry 6 (6). , 2000
PUB | DOI | PubMed | Europe PMC
 
[32]
2000 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397396
The First Synthesis of a 2H-1,4-Benzothiazine-based Phosphine Oxide and Sulfide
Gröger, Harald, The First Synthesis of a 2H-1,4-Benzothiazine-based Phosphine Oxide and Sulfide. Phosphorus, Sulfur, Silicon 166 (). , 2000
PUB
 
[31]
2000 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397409
Preparation of an Enantiomerically Pure Helical Nickel(II) Complex Using a New Chiral Tetradentate Ligand Derived from an Industrial Waste Material
Pennemann, H., Preparation of an Enantiomerically Pure Helical Nickel(II) Complex Using a New Chiral Tetradentate Ligand Derived from an Industrial Waste Material. J. Chem. Soc. Dalton Trans. (). , 2000
PUB
 
[30]
2000 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397430
1,3,5-Triazines, versatile industrial building blocks: Synthetic approaches and applications
Gröger, Harald, 1,3,5-Triazines, versatile industrial building blocks: Synthetic approaches and applications. Chimica Oggi/Chemistry Today 18 (3/4) (). , 2000
PUB
 
[29]
2000 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397352
Concept of Improved Rigidity: How to Make Enantioselective Hydrophosphonylation of Cyclic Imines Catalyzed by Chiral Heterobimetallic Lanthanoid Complexes Almost Perfect
Schlemminger, I., Concept of Improved Rigidity: How to Make Enantioselective Hydrophosphonylation of Cyclic Imines Catalyzed by Chiral Heterobimetallic Lanthanoid Complexes Almost Perfect. J. Org. Chem. 65 (). , 2000
PUB
 
[28]
2000 | Patent | PUB-ID: 2399023
Precursors for PNA-Monomers
Martens, J., Precursors for PNA-Monomers. (). , 2000
PUB
 
[27]
2000 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2397440
Moderne Methoden der Suzuki-Kreuzkupplung: Die langerwarteten universellen Synthesevarianten mit Arylchloriden
Gröger, Harald, Moderne Methoden der Suzuki-Kreuzkupplung: Die langerwarteten universellen Synthesevarianten mit Arylchloriden. J. Prakt. Chem. 342 (). , 2000
PUB
 
[26]
2000 | Patent | PUB-ID: 2399111
Verfahren zur Herstellung von N-Phosphonomethyliminodiessigsäure
Gröger, Harald, Verfahren zur Herstellung von N-Phosphonomethyliminodiessigsäure. (). , 2000
PUB
 
[25]
1999 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2347897
The Asymmetric Nitroaldol Reaction: Addition of Nitroalkanes to Aldehydes in the Presence of Heterobimetallic Lanthanoid Catalysts
Shibasaki, M., The Asymmetric Nitroaldol Reaction: Addition of Nitroalkanes to Aldehydes in the Presence of Heterobimetallic Lanthanoid Catalysts. Comprehensive Asymmetric Catalysis, Vol 3 (). Heidelberg, 1999
PUB
 
[24]
1999 | Zeitschriftenaufsatz | PUB-ID: 2347912
The First Catalytic Asymmetric Nitro-Mannich-type Reaction Promoted by a New Heterobimetallic Complex
Yamada, K.-i., The First Catalytic Asymmetric Nitro-Mannich-type Reaction Promoted by a New Heterobimetallic Complex. Angew. Chem. Int.Ed. 38 (). , 1999
PUB
 
[23]
1999 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2407545
Towards Perfect Asymmetric Catalysis: Additives and Co-catalysts
Vogl, E.M, Towards Perfect Asymmetric Catalysis: Additives and Co-catalysts. Angew. Chem. Int. Ed. 38 (11). , 1999
PUB | DOI | WoS | PubMed | Europe PMC
 
[22]
1999 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2347907
Chiral Heterobimetallic Lanthanoid Complexes: A Highly Efficient Multifunctional Catalyst for the Asymmetric Formation of C-C,C-O, and C-P Bonds
Shibasaki, M., Chiral Heterobimetallic Lanthanoid Complexes: A Highly Efficient Multifunctional Catalyst for the Asymmetric Formation of C-C,C-O, and C-P Bonds. Topics in Organometallic Chemistry: Lanthanides: Chemistry and Use in Organic Synthesis 2 (). Heidelberg, 1999
PUB
 
[21]
1999 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2407465
Erste katalytische asymmetrische Nitro-Mannich-Reaktion mit einem neuen Heterodimetallkomplex des Katalysators
Yamada, Ken-ichi, Erste katalytische asymmetrische Nitro-Mannich-Reaktion mit einem neuen Heterodimetallkomplex des Katalysators. Angewandte Chem. (111). , 1999
PUB
 
[20]
1999 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2407462
Zur Perfektionierung der asymmetrischen Katalyse: Additive und Co-Katalysatoren
Vogl, Erasmus M., Zur Perfektionierung der asymmetrischen Katalyse: Additive und Co-Katalysatoren. Angew. Chem. (111). , 1999
PUB
 
[19]
1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347854
The First Synthesis of Cyclic alpha-Amino Phosphonic Acid Amines Bearing the Benzodiazaphosphorinananone System
Gröger, Harald, The First Synthesis of Cyclic alpha-Amino Phosphonic Acid Amines Bearing the Benzodiazaphosphorinananone System. Heteroatom Chem. 9 (). , 1998
PUB
 
[18]
1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347865
A New and Highly Efficient Route to Cyclic alpha-Amino Phosphonates: The First Catalytic Enantioselective Hydrophosphonylation of Cyclic Imines Catalyzed by Chiral Heterobimetallic Lanthanoid Complexes
Gröger, Harald, A New and Highly Efficient Route to Cyclic alpha-Amino Phosphonates: The First Catalytic Enantioselective Hydrophosphonylation of Cyclic Imines Catalyzed by Chiral Heterobimetallic Lanthanoid Complexes. J. Am. Chem. Soc. 120 (). , 1998
PUB
 
[17]
1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347881
New Catalytic Concepts for the Asymmetric Aldol Reaction
Gröger, Harald, New Catalytic Concepts for the Asymmetric Aldol Reaction. Chem. Eur. J. 4 (). , 1998
PUB
 
[16]
1997 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347828
A Novel Synthetic Approach to alpha-Aminophosphine Sulfide Structures: The First Dimethylphosphine Sulfide Addition to 3-Thiazolines
Gröger, Harald, A Novel Synthetic Approach to alpha-Aminophosphine Sulfide Structures: The First Dimethylphosphine Sulfide Addition to 3-Thiazolines. Phosphorus, Sulfur, Silicon 128 (). , 1997
PUB
 
[15]
1997 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347743
Synthesis and Applilcation of New ß-Amino Alcohols Based on the Octahydrocyclopenta[b]pyrrol System in the Catalytic Enantioselective Addition of Diethylzinc to Benzaldehyde
Wilken, J., Synthesis and Applilcation of New ß-Amino Alcohols Based on the Octahydrocyclopenta[b]pyrrol System in the Catalytic Enantioselective Addition of Diethylzinc to Benzaldehyde. Tetrahedron: Asymmetry 8 (). , 1997
PUB
 
[14]
1997 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347713
Synthesis of Dimethyl 4-Thiazolidinylphosphine Oxides via Addition of Dimethylphosphine Oxide to 3-Thiazolines
Gröger, Harald, Synthesis of Dimethyl 4-Thiazolidinylphosphine Oxides via Addition of Dimethylphosphine Oxide to 3-Thiazolines. Heteroatom Chem. 8 (). , 1997
PUB
 
[13]
1997 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347775
Synthesis and Application of New (threo)- and (erythro)-Amino Alcohols Based on the Octahydro-cyclopenta[b]pyrrol System in the Catalytic Enantioselective Addition of Diethylzinc to Benzaldehyde
Wilken, J., Synthesis and Application of New (threo)- and (erythro)-Amino Alcohols Based on the Octahydro-cyclopenta[b]pyrrol System in the Catalytic Enantioselective Addition of Diethylzinc to Benzaldehyde. Tetrahedron Asymmetry 8 (). , 1997
PUB
 
[12]
1997 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347821
A New Enantioselective Synthetic Approach to ß-Aminothio-compounds via Enantioselective Reduction of N,S-Heterocyclic Imines
Reiners, I., A New Enantioselective Synthetic Approach to ß-Aminothio-compounds via Enantioselective Reduction of N,S-Heterocyclic Imines. J. Prakt. Chem. 339 (). , 1997
PUB
 
[11]
1997 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347759
Synthesis of New, Chiral ß-sec-Amino Alcohols - Diastereodivergent Addition of Grignard-Reagents to a-Amno Aldehydes Based on the (all-R)-2-Azabicyclo[3.3.0]octane-System
Wilken, J., Synthesis of New, Chiral ß-sec-Amino Alcohols - Diastereodivergent Addition of Grignard-Reagents to a-Amno Aldehydes Based on the (all-R)-2-Azabicyclo[3.3.0]octane-System. Liebigs Ann./Recuell (). , 1997
PUB
 
[10]
1997 | Diskussionspapier | Veröffentlicht | PUB-ID: 2347850
Nukleophile Additionsreaktionen an die C=N-Doppelbindung schwefelhaltiger, cyclischer Imine unter Berücksichtigung stereoselektiver Aspekte
Gröger, Harald, Nukleophile Additionsreaktionen an die C=N-Doppelbindung schwefelhaltiger, cyclischer Imine unter Berücksichtigung stereoselektiver Aspekte. (). , 1997
PUB
 
[9]
1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347671
The Totally Protected Hydroxy Containing alpha-Amino Phosphonic Esters and alpha-Amino Phosphinoxides as well as their Carbamoyl Derivatives
Hatam, M., The Totally Protected Hydroxy Containing alpha-Amino Phosphonic Esters and alpha-Amino Phosphinoxides as well as their Carbamoyl Derivatives. Synth. Commun. 26 (). , 1996
PUB
 
[8]
1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344573
Synthese Totalgeschützter Thioanaloga der 1,2,3,4-Tetrahydrochinolin-2-carbonsäure aus 2H-1,4-Benzothiazinen via Ugi-Reaktion
Gröger, Harald, Synthese Totalgeschützter Thioanaloga der 1,2,3,4-Tetrahydrochinolin-2-carbonsäure aus 2H-1,4-Benzothiazinen via Ugi-Reaktion. Sulfur Lett. 19 (). , 1996
PUB
 
[7]
1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347651
Chemistry of the 1,3,5-Triaza-2-phosphorine-4,6-diones, Part XI. Base-Catalyzed Addition Reactions of 2-Oxo-2-hydro-1,3,5-trimethyl-1,3,5-triaza-2I4-phosphorine-4,6-dione to the C-N Double Bond of 3-Thiazoline Heterocycles
Neda, I., Chemistry of the 1,3,5-Triaza-2-phosphorine-4,6-diones, Part XI. Base-Catalyzed Addition Reactions of 2-Oxo-2-hydro-1,3,5-trimethyl-1,3,5-triaza-2I4-phosphorine-4,6-dione to the C-N Double Bond of 3-Thiazoline Heterocycles. Z. Naturforsch. 51b (). , 1996
PUB
 
[6]
1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344556
Synthesis of New 4-Thiazolidinylphosphonates via Stereoselective Pudovik Reaction
Gröger, Harald, Synthesis of New 4-Thiazolidinylphosphonates via Stereoselective Pudovik Reaction. Synth. Commun. 26 (). , 1996
PUB
 
[5]
1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344599
Synthetic Approach to New alpha-Aminophosphonates Derived from Six-Membered, Sulfur-Containing Heterocyclic Imines
Gröger, Harald, Synthetic Approach to New alpha-Aminophosphonates Derived from Six-Membered, Sulfur-Containing Heterocyclic Imines. Phosphorus, Sulfur, Silicon 116 (). , 1996
PUB
 
[4]
1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347629
Stereoselektive Pudovik-Reaktion von 5,6-Benzo-2H-1-methyl-3-(2'-chlorethyl)-2-oxo-1,3,2I4-diazaphosphorin-4-on mit einem 3-Thiazolin und MPL-Chromatographische Isolierung des Überschußdiastereomers
Gröger, Harald, Stereoselektive Pudovik-Reaktion von 5,6-Benzo-2H-1-methyl-3-(2'-chlorethyl)-2-oxo-1,3,2I4-diazaphosphorin-4-on mit einem 3-Thiazolin und MPL-Chromatographische Isolierung des Überschußdiastereomers. Z. Naturforsch. 51b (). , 1996
PUB
 
[3]
1996 | Zeitschriftenaufsatz | PUB-ID: 2344586
Synthesis of Glutathione Analogues, Peptide Nucleic Acids and Phosphono-oligopetides from Heterocyclic Imines
Gröger, Harald, Synthesis of Glutathione Analogues, Peptide Nucleic Acids and Phosphono-oligopetides from Heterocyclic Imines. Synth. Commun. 26 (). , 1996
PUB
 
[2]
1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2347696
First Catalytic Asymmetric Hydrophosphonylation of Cyclilc Imines: Highly Efficient Enantioselective Approach to a 4-Thiazolidinylphosphonate via Chiral Titanium and Lanthanoid Catalysts
Gröger, Harald, First Catalytic Asymmetric Hydrophosphonylation of Cyclilc Imines: Highly Efficient Enantioselective Approach to a 4-Thiazolidinylphosphonate via Chiral Titanium and Lanthanoid Catalysts. Tetrahedron Lett. 37 (). , 1996
PUB
 
[1]
1995 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2344535
Synthese Totalgeschützter, Nichtproteinogener alpha-Aminosäuren und Oligopeptide aus 2H-1,3-Oxazinen und 2H-1,3-Bezoxazinen via Ugi-Reaction
Gröger, Harald, Synthese Totalgeschützter, Nichtproteinogener alpha-Aminosäuren und Oligopeptide aus 2H-1,3-Oxazinen und 2H-1,3-Bezoxazinen via Ugi-Reaction. Tetrahedron 51 (). , 1995
PUB
 

Suche

Publikationen filtern

Darstellung / Sortierung

Zitationsstil: default

Export / Einbettung