Catalytic enantioselective Strecker reactions and analogous syntheses

Gröger H (2003)
Chemical Reviews 103(8): 2795-2828.

Es wurde kein Volltext hochgeladen. Nur Publikationsnachweis!
Zeitschriftenaufsatz | Veröffentlicht | Englisch
Chemical Reviews


Gröger H. Catalytic enantioselective Strecker reactions and analogous syntheses. Chemical Reviews. 2003;103(8):2795-2828.
Gröger, H. (2003). Catalytic enantioselective Strecker reactions and analogous syntheses. Chemical Reviews, 103(8), 2795-2828. doi:10.1021/cr020038p
Gröger, H. (2003). Catalytic enantioselective Strecker reactions and analogous syntheses. Chemical Reviews 103, 2795-2828.
Gröger, H., 2003. Catalytic enantioselective Strecker reactions and analogous syntheses. Chemical Reviews, 103(8), p 2795-2828.
H. Gröger, “Catalytic enantioselective Strecker reactions and analogous syntheses”, Chemical Reviews, vol. 103, 2003, pp. 2795-2828.
Gröger, H.: Catalytic enantioselective Strecker reactions and analogous syntheses. Chemical Reviews. 103, 2795-2828 (2003).
Gröger, Harald. “Catalytic enantioselective Strecker reactions and analogous syntheses”. Chemical Reviews 103.8 (2003): 2795-2828.

106 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

Highly Stereoselective Strecker Synthesis Induced by a Slight Modification of Benzhydrylamine from Achiral to Chiral.
Takamatsu N, Aiba S, Yamada T, Tokunaga Y, Kawasaki T., Chemistry 24(6), 2018
PMID: 28980348
Retrosynthesis of multi-component metal-organic frameworks.
Yuan S, Qin JS, Li J, Huang L, Feng L, Fang Y, Lollar C, Pang J, Zhang L, Sun D, Alsalme A, Cagin T, Zhou HC., Nat Commun 9(1), 2018
PMID: 29476174
Biocatalytic Synthesis of Nitriles through Dehydration of Aldoximes: The Substrate Scope of Aldoxime Dehydratases.
Betke T, Higuchi J, Rommelmann P, Oike K, Nomura T, Kato Y, Asano Y, Gröger H., Chembiochem 19(8), 2018
PMID: 29333684
The Strecker reaction coupled to Viedma ripening: a simple route to highly hindered enantiomerically pure amino acids.
Baglai I, Leeman M, Wurst K, Kaptein B, Kellogg RM, Noorduin WL., Chem Commun (Camb) 54(77), 2018
PMID: 30159569
Enantioselective synthesis of α-perfluoroalkylated prolines, their 6,7-membered homologues and derivatives.
Voznesenskaia NG, Shmatova OI, Khrustalev VN, Nenajdenko VG., Org Biomol Chem 16(38), 2018
PMID: 30229784
The asymmetric reduction of imidazolinones with trichlorosilane.
Wagner C, Kotthaus AF, Kirsch SF., Chem Commun (Camb) 53(32), 2017
PMID: 28387397
Enantioselective synthesis of pyrazolone α-aminonitrile derivatives via an organocatalytic Strecker reaction.
Mahajan S, Chauhan P, Kaya U, Deckers K, Rissanen K, Enders D., Chem Commun (Camb) 53(49), 2017
PMID: 28585622
Aminomethylation of Aryl Halides using α-Silylamines Enabled by Ni/Photoredox Dual Catalysis.
Remeur C, Kelly CB, Patel NR, Molander GA., ACS Catal 7(9), 2017
PMID: 29354317
Cyanide-Free and Broadly Applicable Enantioselective Synthetic Platform for Chiral Nitriles through a Biocatalytic Approach.
Betke T, Rommelmann P, Oike K, Asano Y, Gröger H., Angew Chem Int Ed Engl 56(40), 2017
PMID: 28671741
Visible-light photoredox synthesis of unnatural chiral α-amino acids.
Jiang M, Jin Y, Yang H, Fu H., Sci Rep 6(), 2016
PMID: 27185220
Stereoselective Synthesis of α-Amino-C-phosphinic Acids and Derivatives.
Viveros-Ceballos JL, Ordóñez M, Sayago FJ, Cativiela C., Molecules 21(9), 2016
PMID: 27589703
Design, synthesis, anticancer, antimicrobial activities and molecular docking studies of novel quinoline bearing dihydropyridines.
Nkosi SM, Anand K, Anandakumar S, Singh S, Chuturgoon AA, Gengan RM., J Photochem Photobiol B 165(), 2016
PMID: 27871033
A theoretical study of imine hydrocyanation catalyzed by halogen-bonding.
Heinz N, Dolg M, Berkessel A., J Comput Chem 36(24), 2015
PMID: 26149792
Design, synthesis, acetylcholinesterase inhibition and larvicidal activity of girgensohnine analogs on Aedes aegypti, vector of dengue fever.
Carreño Otero AL, Vargas Méndez LY, Duque L JE, Kouznetsov VV., Eur J Med Chem 78(), 2014
PMID: 24704612
Catalytic functionalization of tertiary alcohols to fully substituted carbon centres.
Chen L, Yin XP, Wang CH, Zhou J., Org Biomol Chem 12(32), 2014
PMID: 24915514
Direct nucleophilic addition to N-alkoxyamides.
Yanagita Y, Nakamura H, Shirokane K, Kurosaki Y, Sato T, Chida N., Chemistry 19(2), 2013
PMID: 23165728
A synthesis of α-amino acids via direct reductive carboxylation of imines with carbon dioxide.
Sathe AA, Hartline DR, Radosevich AT., Chem Commun (Camb) 49(44), 2013
PMID: 23620277
Enantioselective cyanoethoxycarbonylation of isatins promoted by a Lewis base-Brønsted acid cooperative catalyst.
Ogura Y, Akakura M, Sakakura A, Ishihara K., Angew Chem Int Ed Engl 52(32), 2013
PMID: 23824788
Oxazoline-based organocatalyst for enantioselective strecker reactions: a protocol for the synthesis of levamisole.
Sadhukhan A, Sahu D, Ganguly B, Khan NU, Kureshy RI, Abdi SH, Suresh E, Bajaj HC., Chemistry 19(42), 2013
PMID: 24009109
Squaramide-catalyzed enantioselective Michael addition of masked acyl cyanides to substituted enones.
Yang KS, Nibbs AE, Türkmen YE, Rawal VH., J Am Chem Soc 135(43), 2013
PMID: 24090310
Asymmetric organocatalytic Strecker-type reactions of aliphatic N,N-dialkylhydrazones.
Martínez-Muñoz A, Monge D, Martín-Zamora E, Marqués-López E, Álvarez E, Fernández R, Lassaletta JM., Org Biomol Chem 11(47), 2013
PMID: 24165968
Biological activity of Fe(III) aquo-complexes towards ferric chelate reductase (FCR).
Escudero R, Gómez-Gallego M, Romano S, Fernández I, Gutiérrez-Alonso Á, Sierra MA, López-Rayo S, Nadal P, Lucena JJ., Org Biomol Chem 10(11), 2012
PMID: 22314341
Synthesis, characterization and catalytic activity of lithium and sodium iminophenoxide complexes towards ring-opening polymerization of L-lactide.
Lu WY, Hsiao MW, Hsu SC, Peng WT, Chang YJ, Tsou YC, Wu TY, Lai YC, Chen Y, Chen HY., Dalton Trans 41(13), 2012
PMID: 22333925
A highly enantioselective catalytic Strecker reaction of cyclic (Z)-aldimines.
Shao YD, Tian SK., Chem Commun (Camb) 48(40), 2012
PMID: 22499398
Copper-catalyzed α-amination of aliphatic aldehydes.
Tian JS, Loh TP., Chem Commun (Camb) 47(19), 2011
PMID: 21475752
Mechanistic considerations of guanidine-catalyzed reactions.
Fu X, Tan CH., Chem Commun (Camb) 47(29), 2011
PMID: 21541409
Racemase activity of B. cepacia lipase leads to dual-function asymmetric dynamic kinetic resolution of α-aminonitriles.
Vongvilai P, Linder M, Sakulsombat M, Svedendahl Humble M, Berglund P, Brinck T, Ramström O., Angew Chem Int Ed Engl 50(29), 2011
PMID: 21633990
Addition of TMSCN to chiral ketimines derived from isatin. Synthesis of an oxindole-based peptidomimetic and a bioactive spirohydantoin.
Sacchetti A, Silvani A, Gatti FG, Lesma G, Pilati T, Trucchi B., Org Biomol Chem 9(15), 2011
PMID: 21687843
A simple method for the determination of enantiomeric excess and identity of chiral carboxylic acids.
Joyce LA, Maynor MS, Dragna JM, da Cruz GM, Lynch VM, Canary JW, Anslyn EV., J Am Chem Soc 133(34), 2011
PMID: 21780788
C-branched chiral (racemic) macrocyclic amino acids: structure of their Ni(II), Zn(II) and Cu(II) complexes.
Pellico D, Gómez-Gallego M, Escudero R, Ramírez-López P, Oliván M, Sierra MA., Dalton Trans 40(36), 2011
PMID: 21822522
A truly green synthesis of α-aminonitriles via Strecker reaction.
Bandyopadhyay D, Velazquez JM, Banik BK., Org Med Chem Lett 1(1), 2011
PMID: 22373109
Brønsted acid-catalyzed efficient Strecker reaction of ketones, amines and trimethylsilyl cyanide.
Zhang GW, Zheng DH, Nie J, Wang T, Ma JA., Org Biomol Chem 8(6), 2010
PMID: 20204214
A facile method for the synthesis of oxindole based quaternary alpha-aminonitriles via the Strecker reaction.
Liu YL, Zhou F, Cao JJ, Ji CB, Ding M, Zhou J., Org Biomol Chem 8(17), 2010
PMID: 20617240
A direct entry to substituted N-methoxyamines from N-methoxyamides via N-oxyiminium ions.
Shirokane K, Kurosaki Y, Sato T, Chida N., Angew Chem Int Ed Engl 49(36), 2010
PMID: 20672260
Chiral BINOL-derived phosphoric acids: privileged Brønsted acid organocatalysts for C-C bond formation reactions.
Zamfir A, Schenker S, Freund M, Tsogoeva SB., Org Biomol Chem 8(23), 2010
PMID: 20820680
Asymmetric organocatalysis by chiral Brønsted bases: implications and applications.
Palomo C, Oiarbide M, López R., Chem Soc Rev 38(2), 2009
PMID: 19169469
Chiral guanidine catalyzed enantioselective reactions.
Leow D, Tan CH., Chem Asian J 4(4), 2009
PMID: 19101939
Efficient three-component Strecker reaction of aldehydes/ketones via NHC-amidate palladium(II) complex catalysis.
Jarusiewicz J, Choe Y, Yoo KS, Park CP, Jung KW., J Org Chem 74(7), 2009
PMID: 19265413
Facile and efficient enantioselective Strecker reaction of ketimines by chiral sodium phosphate.
Shen K, Liu X, Cai Y, Lin L, Feng X., Chemistry 15(24), 2009
PMID: 19418513
Amide-based bifunctional organocatalysts in asymmetric reactions.
Liu X, Lin L, Feng X., Chem Commun (Camb) (41), 2009
PMID: 19826653
Scaleable catalytic asymmetric Strecker syntheses of unnatural alpha-amino acids.
Zuend SJ, Coughlin MP, Lalonde MP, Jacobsen EN., Nature 461(7266), 2009
PMID: 19829379
Enantioselective C--C bond formation to sulfonylimines through use of the 2-pyridinesulfonyl group as a novel stereocontroller.
Nakamura S, Nakashima H, Sugimoto H, Sano H, Hattori M, Shibata N, Toru T., Chemistry 14(7), 2008
PMID: 18081110
Lewis base catalysis in organic synthesis.
Denmark SE, Beutner GL., Angew Chem Int Ed Engl 47(9), 2008
PMID: 18236505
Efficient kinetic resolution of racemic amino aldehydes by oxidation with N-iodosuccinimide.
Minato D, Nagasue Y, Demizu Y, Onomura O., Angew Chem Int Ed Engl 47(49), 2008
PMID: 18973218
The catalytic acylcyanation of imines.
Pan SC, List B., Chem Asian J 3(2), 2008
PMID: 18203214
Facile one-pot synthesis of 5-substituted hydantoins.
Murray RG, Whitehead DM, Le Strat F, Conway SJ., Org Biomol Chem 6(6), 2008
PMID: 18327322
Discovery of amino-acetonitrile derivatives, a new class of synthetic anthelmintic compounds.
Ducray P, Gauvry N, Pautrat F, Goebel T, Fruechtel J, Desaules Y, Weber SS, Bouvier J, Wagner T, Froelich O, Kaminsky R., Bioorg Med Chem Lett 18(9), 2008
PMID: 18400497
Synthesis and antibacterial evaluation of a novel series of rifabutin-like spirorifamycins.
Kim IH, Combrink KD, Ma Z, Chapo K, Yan D, Renick P, Morris TW, Pulse M, Simecka JW, Ding CZ., Bioorg Med Chem Lett 17(5), 2007
PMID: 17189695
Catalytic asymmetric acylcyanation of imines.
Pan SC, Zhou J, List B., Angew Chem Int Ed Engl 46(4), 2007
PMID: 17154433
Enantioselective strecker reaction catalyzed by an organocatalyst lacking a hydrogen-bond-donor function.
Negru M, Schollmeyer D, Kunz H., Angew Chem Int Ed Engl 46(48), 2007
PMID: 17968869
A highly enantioselective Brønsted acid catalyst for the Strecker reaction.
Rueping M, Sugiono E, Azap C., Angew Chem Int Ed Engl 45(16), 2006
PMID: 16544358
Chiral poly-rare earth metal complexes in asymmetric catalysis.
Shibasaki M., Proc Jpn Acad Ser B Phys Biol Sci 82(2), 2006
PMID: 25792774
Asymmetric multicomponent reactions (AMCRs): the new frontier.
Ramón DJ, Yus M., Angew Chem Int Ed Engl 44(11), 2005
PMID: 15719349
Highly enantioselective organocatalytic hydroxyalkylation of indoles with ethyl trifluoropyruvate.
Török B, Abid M, London G, Esquibel J, Török M, Mhadgut SC, Yan P, Prakash GK., Angew Chem Int Ed Engl 44(20), 2005
PMID: 15844111


Markieren/ Markierung löschen
Markierte Publikationen

Open Data PUB

Web of Science

Dieser Datensatz im Web of Science®


PMID: 12914481
PubMed | Europe PMC

Suchen in

Google Scholar