The Pentamethylcyclopentadienylsilicon(II) Cation as a Catalyst for the Specific Degradation of Oligo(ethyleneglycol) Diethers
Leszczynska K, Mix A, Berger R, Rummel B, Neumann B, Stammler H-G, Jutzi P (2011)
Angewandte Chemie International Edition 50(30): 6843-6846.
Zeitschriftenaufsatz
| Veröffentlicht | Englisch
Download
Es wurden keine Dateien hochgeladen. Nur Publikationsnachweis!
Autor*in
Leszczynska, Kinga;
Mix, AndreasUniBi;
Berger, RaphaelUniBi 
;
Rummel, BrittaUniBi;
Neumann, BeateUniBi;
Stammler, Hans-GeorgUniBi;
Jutzi, PeterUniBi
;
Rummel, BrittaUniBi;
Neumann, BeateUniBi;
Stammler, Hans-GeorgUniBi;
Jutzi, PeterUniBiStichworte
crown ether ligands;
oligoether degradation;
pi;
silicon(II) compounds;
complexes;
homogeneous catalysis
Erscheinungsjahr
2011
Zeitschriftentitel
Angewandte Chemie International Edition
Band
50
Ausgabe
30
Seite(n)
6843-6846
ISSN
1433-7851
Page URI
https://pub.uni-bielefeld.de/record/2307397
Zitieren
Leszczynska K, Mix A, Berger R, et al. The Pentamethylcyclopentadienylsilicon(II) Cation as a Catalyst for the Specific Degradation of Oligo(ethyleneglycol) Diethers. Angewandte Chemie International Edition. 2011;50(30):6843-6846.
Leszczynska, K., Mix, A., Berger, R., Rummel, B., Neumann, B., Stammler, H. - G., & Jutzi, P. (2011). The Pentamethylcyclopentadienylsilicon(II) Cation as a Catalyst for the Specific Degradation of Oligo(ethyleneglycol) Diethers. Angewandte Chemie International Edition, 50(30), 6843-6846. https://doi.org/10.1002/anie.201101139
Leszczynska, Kinga, Mix, Andreas, Berger, Raphael, Rummel, Britta, Neumann, Beate, Stammler, Hans-Georg, and Jutzi, Peter. 2011. “The Pentamethylcyclopentadienylsilicon(II) Cation as a Catalyst for the Specific Degradation of Oligo(ethyleneglycol) Diethers”. Angewandte Chemie International Edition 50 (30): 6843-6846.
Leszczynska, K., Mix, A., Berger, R., Rummel, B., Neumann, B., Stammler, H. - G., and Jutzi, P. (2011). The Pentamethylcyclopentadienylsilicon(II) Cation as a Catalyst for the Specific Degradation of Oligo(ethyleneglycol) Diethers. Angewandte Chemie International Edition 50, 6843-6846.
Leszczynska, K., et al., 2011. The Pentamethylcyclopentadienylsilicon(II) Cation as a Catalyst for the Specific Degradation of Oligo(ethyleneglycol) Diethers. Angewandte Chemie International Edition, 50(30), p 6843-6846.
K. Leszczynska, et al., “The Pentamethylcyclopentadienylsilicon(II) Cation as a Catalyst for the Specific Degradation of Oligo(ethyleneglycol) Diethers”, Angewandte Chemie International Edition, vol. 50, 2011, pp. 6843-6846.
Leszczynska, K., Mix, A., Berger, R., Rummel, B., Neumann, B., Stammler, H.-G., Jutzi, P.: The Pentamethylcyclopentadienylsilicon(II) Cation as a Catalyst for the Specific Degradation of Oligo(ethyleneglycol) Diethers. Angewandte Chemie International Edition. 50, 6843-6846 (2011).
Leszczynska, Kinga, Mix, Andreas, Berger, Raphael, Rummel, Britta, Neumann, Beate, Stammler, Hans-Georg, and Jutzi, Peter. “The Pentamethylcyclopentadienylsilicon(II) Cation as a Catalyst for the Specific Degradation of Oligo(ethyleneglycol) Diethers”. Angewandte Chemie International Edition 50.30 (2011): 6843-6846.
Daten bereitgestellt von European Bioinformatics Institute (EBI)
7 Zitationen in Europe PMC
Daten bereitgestellt von Europe PubMed Central.
The Parent Cyclopentadienyltin Cation, Its Toluene Adduct, and the Quadruple-Decker [Sn3 Cp4 ]2.
Schleep M, Hettich C, Velázquez Rojas J, Kratzert D, Ludwig T, Lieberth K, Krossing I., Angew Chem Int Ed Engl 56(11), 2017
PMID: 28177204
Schleep M, Hettich C, Velázquez Rojas J, Kratzert D, Ludwig T, Lieberth K, Krossing I., Angew Chem Int Ed Engl 56(11), 2017
PMID: 28177204
Polyether complexes of groups 13 and 14.
Swidan A, Macdonald CL., Chem Soc Rev 45(14), 2016
PMID: 27063465
Swidan A, Macdonald CL., Chem Soc Rev 45(14), 2016
PMID: 27063465
Cations and dications of heavier group 14 elements in low oxidation states.
Swamy VS, Pal S, Khan S, Sen SS., Dalton Trans 44(29), 2015
PMID: 26084389
Swamy VS, Pal S, Khan S, Sen SS., Dalton Trans 44(29), 2015
PMID: 26084389
The pentamethylcyclopentadienylsilicon(II) cation: synthesis, characterization, and reactivity.
Jutzi P., Chemistry 20(30), 2014
PMID: 24986115
Jutzi P., Chemistry 20(30), 2014
PMID: 24986115
A facile access to a novel NHC-stabilized silyliumylidene ion and C-H activation of phenylacetylene.
Ahmad SU, Szilvási T, Inoue S., Chem Commun (Camb) 50(84), 2014
PMID: 25073116
Ahmad SU, Szilvási T, Inoue S., Chem Commun (Camb) 50(84), 2014
PMID: 25073116
"Tamed" silylium ions: versatile in catalysis.
Schulz A, Villinger A., Angew Chem Int Ed Engl 51(19), 2012
PMID: 22422647
Schulz A, Villinger A., Angew Chem Int Ed Engl 51(19), 2012
PMID: 22422647
The elusive silyliumylidene [ClSi:]+ and silathionium [ClSi=S]+ cations stabilized by bis(iminophosphorane) chelate ligand.
Xiong Y, Yao S, Inoue S, Irran E, Driess M., Angew Chem Int Ed Engl 51(40), 2012
PMID: 22965539
Xiong Y, Yao S, Inoue S, Irran E, Driess M., Angew Chem Int Ed Engl 51(40), 2012
PMID: 22965539
35 References
Daten bereitgestellt von Europe PubMed Central.
Carbon-carbon bond forming reactions mediated by silicon Lewis acids.
Dilman AD, Ioffe SL., Chem. Rev. 103(3), 2003
PMID: 12630851
Dilman AD, Ioffe SL., Chem. Rev. 103(3), 2003
PMID: 12630851
AUTHOR UNKNOWN, 0
Lambert, J. Am. Chem. Soc. 121(), 1999
Lambert, J. Phys. Org. Chem. 14(), 2001
AUTHOR UNKNOWN, 0
Crystal structure of a silyl cation with no coordination to anion and distant coordination to solvent.
Lambert JB, Zhang S, Stern CL, Huffman JC., Science 260(5116), 1993
PMID: 17836721
Lambert JB, Zhang S, Stern CL, Huffman JC., Science 260(5116), 1993
PMID: 17836721
beta-Silyl and beta-Germyl Carbocations Stable at Room Temperature.
Lambert JB, Zhao Y, Wu H., J. Org. Chem. 64(8), 1999
PMID: 11674342
Lambert JB, Zhao Y, Wu H., J. Org. Chem. 64(8), 1999
PMID: 11674342
Strong counteranion effects on the catalytic activity of cationic silicon Lewis acids in Mukaiyama aldol and Diels-Alder reactions.
Hara K, Akiyama R, Sawamura M., Org. Lett. 7(25), 2005
PMID: 16321006
Hara K, Akiyama R, Sawamura M., Org. Lett. 7(25), 2005
PMID: 16321006
Room-temperature catalytic hydrodefluorination of C(sp3)-F bonds.
Scott VJ, Celenligil-Cetin R, Ozerov OV., J. Am. Chem. Soc. 127(9), 2005
PMID: 15740111
Scott VJ, Celenligil-Cetin R, Ozerov OV., J. Am. Chem. Soc. 127(9), 2005
PMID: 15740111
Isolating fluorinated carbocations.
Douvris C, Stoyanov ES, Tham FS, Reed CA., Chem. Commun. (Camb.) (11), 2007
PMID: 17347720
Douvris C, Stoyanov ES, Tham FS, Reed CA., Chem. Commun. (Camb.) (11), 2007
PMID: 17347720
Hydrodefluorination of perfluoroalkyl groups using silylium-carborane catalysts.
Douvris C, Ozerov OV., Science 321(5893), 2008
PMID: 18755971
Douvris C, Ozerov OV., Science 321(5893), 2008
PMID: 18755971
AUTHOR UNKNOWN, 0
Kira, Chem. Lett. (), 1992
Studies on the mechanism of B(C(6)F(5))(3)-catalyzed hydrosilation of carbonyl functions
Parks DJ, Blackwell JM, Piers WE., J. Org. Chem. 65(10), 2000
PMID: 10814201
Parks DJ, Blackwell JM, Piers WE., J. Org. Chem. 65(10), 2000
PMID: 10814201
Hydrogen- and fluorine-bridged disilyl cations and their use in catalytic C-F activation.
Panisch R, Bolte M, Muller T., J. Am. Chem. Soc. 128(30), 2006
PMID: 16866520
Panisch R, Bolte M, Muller T., J. Am. Chem. Soc. 128(30), 2006
PMID: 16866520
Klare, Angew. Chem. 121(), 2009
Taming the silylium ion for low-temperature Diels-Alder reactions.
Klare HF, Bergander K, Oestreich M., Angew. Chem. Int. Ed. Engl. 48(48), 2009
PMID: 19862787
Klare HF, Bergander K, Oestreich M., Angew. Chem. Int. Ed. Engl. 48(48), 2009
PMID: 19862787
Self-regeneration of a silylium ion catalyst in carbonyl reduction.
Muther K, Oestreich M., Chem. Commun. (Camb.) 47(1), 2010
PMID: 20737081
Muther K, Oestreich M., Chem. Commun. (Camb.) 47(1), 2010
PMID: 20737081
The (Me5C5)Si+ cation: a stable derivative of HSi+.
Jutzi P, Mix A, Rummel B, Schoeller WW, Neumann B, Stammler HG., Science 305(5685), 2004
PMID: 15232074
Jutzi P, Mix A, Rummel B, Schoeller WW, Neumann B, Stammler HG., Science 305(5685), 2004
PMID: 15232074
Novel pi-complexes of divalent silicon: mixed substituted neutral sandwich compounds and the half-sandwich cation (iPr5C5)Si+.
Jutzi P, Mix A, Neumann B, Rummel B, Stammler HG., Chem. Commun. (Camb.) (33), 2006
PMID: 16921431
Jutzi P, Mix A, Neumann B, Rummel B, Stammler HG., Chem. Commun. (Camb.) (33), 2006
PMID: 16921431
Driess, Angew. Chem. 118(), 2006
Low-valent silicon cations with two-coordinate silicon and aromatic character.
Driess M, Yao S, Brym M, van Wullen C., Angew. Chem. Int. Ed. Engl. 45(40), 2006
PMID: 16986190
Driess M, Yao S, Brym M, van Wullen C., Angew. Chem. Int. Ed. Engl. 45(40), 2006
PMID: 16986190
Rossi, Chem. Mater. 18(), 2006
AUTHOR UNKNOWN, 0
Berger, Silicon 2(), 2010
AUTHOR UNKNOWN, 0
AUTHOR UNKNOWN, 0
Gautret, Synth. Commun. 26(), 1996
AUTHOR UNKNOWN, 0
Larock, 1999
AUTHOR UNKNOWN, 0
Levi, Izv. Akad. Nauk SSSR Ser. Khim. (), 1977
Export
Markieren/ Markierung löschen
Markierte Publikationen
Web of Science
Dieser Datensatz im Web of Science®Quellen
PMID: 21656879
PubMed | Europe PMC
Suchen in
Google Scholar