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B. Martín‐Matute, M. Edin, Krisztián Bogár, J. Bäckvall (2004)
Highly compatible metal and enzyme catalysts for efficient dynamic kinetic resolution of alcohols at ambient temperature.Angewandte Chemie, 43 47
H. Gröger, Francoise-Christine Chamouleau, Nicolas Orologas, Claudia Rollmann, Karlheinz Drauz, W. Hummel, Andrea Weckbecker, O. May (2006)
Enantioselektive Ketonreduktion mit “Designerzellen” bei hohen Substratkonzentrationen: hocheffizienter Zugang zu funktionalisierten optisch aktiven Alkoholen†Angewandte Chemie, 118
Murillo Filho, Thomas Stillger, Michael Müller, A. Liese, C. Wandrey (2003)
Is logP a convenient criterion to guide the choice of solvents for biphasic enzymatic reactions?Angewandte Chemie, 42 26
J. Wallace, B. Baldwin, J. Morrow (1992)
Separation of remote diol and triol stereoisomers by enzyme-catalyzed esterification in organic media or hydrolysis in aqueous mediaJournal of Organic Chemistry, 57
P. Ramachandran, Guangfu Chen, Zhi-Hui Lu, H. Brown (1996)
An efficient preparation of optically pure C2-symmetric aromatic diols by the asymmetric reduction of diacylaromatic compounds with B-chlorodiisopinocampheylborane☆Tetrahedron Letters, 37
P. Anastas, L. Heine, T. Williamson (2000)
Green chemical syntheses and processes
M. Makkee, A. Kieboom, H. Bekkum (1985)
Combined action of an enzyme and a metal catalyst on the conversion of d-glucose/d-fructose mixtures into d-mannitolCarbohydrate Research, 138
G. Gonzalo, I. Lavandera, K. Faber, W. Kroutil (2007)
Enzymatic reduction of ketones in "micro-aqueous" media catalyzed by ADH-A from Rhodococcus ruber.Organic letters, 9 11
H. Gröger, F. Chamouleau, Nicolas Orologas, Claudia Rollmann, K. Drauz, W. Hummel, A. Weckbecker, O. May (2006)
Enantioselective reduction of ketones with "designer cells" at high substrate concentrations: highly efficient access to functionalized optically active alcohols.Angewandte Chemie, 45 34
Csaba Paizs, A. Katona, J. Rétey (2006)
Chemoenzymatic One-Pot Synthesis of Enantiopure L-Arylalanines from ArylaldehydesEuropean Journal of Organic Chemistry, 2006
H. Gröger (2000)
Moderne Methoden der Suzuki-Kreuzkupplung: Die langerwarteten universellen Synthesevarianten mit ArylchloridenJournal Fur Praktische Chemie-chemiker-zeitung, 342
Anna Larsson, B. Persson, Jan-E. Bäckvall (1997)
ENZYMATISCHE RACEMATSPALTUNG VON ALKOHOLEN GEKOPPELT MIT RUTHENIUM-KATALYSIERTER RACEMISIERUNG DES SUBSTRAT-ALKOHOLSAngewandte Chemie, 109
H. Gijsen, Chi‐Huey Wong (1995)
Synthesis of a Cyclitol via a Tandem Enzymatic Aldol - Intramolecular Horner-Wadsworth-Emmons ReactionTetrahedron Letters, 36
A. Berkessel, Claudia Rollmann, F. Chamouleau, Stefanie Labs, O. May, H. Gröger (2007)
Practical Two‐Step Synthesis of an Enantiopure Aliphatic Terminal (S)‐Epoxide Based on Reduction of Haloalkanones with “Designer Cells”Advanced Synthesis & Catalysis, 349
M. Wolberg, W. Hummel, C. Wandrey, Michael Müller (2000)
Highly Regio- and Enantioselective Reduction of 3,5-Dioxocarboxylates.Angewandte Chemie, 39 23
J. Tsuji* (2005)
Palladium Reagents and Catalysts: New Perspectives for the 21st Century
D. Enders, Christoph Grondal, Matthias Hüttl (2007)
Asymmetrische organokatalytische DominoreaktionenAngewandte Chemie, 119
A. Berkessel, M. Sebastian-Ibarz, T. Müller (2006)
Lipase/aluminum-catalyzed dynamic kinetic resolution of secondary alcohols.Angewandte Chemie, 45 39
W. Stampfer, B. Kosjek, K. Faber, W. Kroutil (2003)
Biocatalytic asymmetric hydrogen transfer employing Rhodococcus ruber DSM 44541.The Journal of organic chemistry, 68 2
D. Enders, Christoph Grondal, Matthias Hüttl (2007)
Asymmetric organocatalytic domino reactions.Angewandte Chemie, 46 10
R. Schoevaart, T. Kieboom (2002)
Combined catalytic conversion involving an enzyme, a homogeneous and a heterogeneous catalyst: one-pot preparation of 4-deoxy-d-glucose derivatives from d-galactoseTetrahedron Letters, 43
P. Dinh, J. Howarth, A. Hudnott, Jonathan Williams, W. Harris (1996)
Catalytic racemisation of alcohols: Applications to enzymatic resolution reactionsTetrahedron Letters, 37
A. Liese, K. Seelbach, C. Wandrey (2006)
Industrial Biotransformations: LIESE: INDUSTRIAL BIOTRANSFORMATIONS O-BK
N. Kizaki, Y. Yasohara, J. Hasegawa, M. Wada, M. Kataoka, Sakayu Shimizu (2001)
Synthesis of optically pure ethyl (S)-4-chloro-3-hydroxybutanoate by Escherichia coli transformant cells coexpressing the carbonyl reductase and glucose dehydrogenase genesApplied Microbiology and Biotechnology, 55
Holger Pfründer, Maya Amidjojo, U. Kragl, D. Weuster-Botz (2004)
Effiziente Ganzzell‐Biotransformation im zweiphasigen System ionische Flüssigkeit/WasserAngewandte Chemie, 116
A. Larsson, B. Persson, J. Bäckvall (1997)
Enzymatic Resolution of Alcohols Coupled with Ruthenium‐Catalyzed Racemization of the Substrate AlcoholAngewandte Chemie, 36
Joanne Allen, Jonathan Williams (1996)
Dynamic kinetic resolution with enzyme and palladium combinationsTetrahedron Letters, 37
B. Persson, Anna Larsson, Mikaël Ray, J. Bäckvall (1999)
Ruthenium- and enzyme-catalyzed dynamic kinetic resolution of secondary alcoholsJournal of the American Chemical Society, 121
A. Bruggink, R. Schoevaart, T. Kieboom (2003)
Concepts of Nature in Organic Synthesis: Cascade Catalysis and Multistep Conversions in ConcertChemInform, 34
H. Gröger, Claudia Rollmann, F. Chamouleau, Isabelle Sébastien, O. May, W. Wienand, K. Drauz (2007)
Enantioselective reduction of 4-fluoroacetophenone at high substrate concentration using a tailor-made recombinant whole-cell catalystAdvanced Synthesis & Catalysis, 349
W. Herrmann (2008)
The Suzuki Cross‐CouplingChemInform, 34
A. Berkessel, M. Sebastian‐Ibarz, Thomas Müller (2006)
Lipase/Aluminium-katalysierte dynamische kinetische Racematspaltung von sekundären Alkoholen†Angewandte Chemie, 118
H. Gröger, W. Hummel, Claudia Rollmann, F. Chamouleau, H. Huesken, Helge Werner, C. Wunderlich, Kofi Abokitse, K. Drauz, S. Buchholz (2004)
Preparative asymmetric reduction of ketones in a biphasic medium with an (S)-alcohol dehydrogenase under in situ-cofactor-recycling with a formate dehydrogenaseTetrahedron, 60
Kyoko Yamamoto, Masataka Watanabe, Kyoko Ideta, S. Mataka*, T. Thiemann (2005)
Combined Suzuki Coupling – Wittig Olefination Reaction in Aqueous MediumZeitschrift für Naturforschung B, 60
H. Pfruender, M. Amidjojo, U. Kragl, D. Weuster‐Botz (2004)
Efficient whole-cell biotransformation in a biphasic ionic liquid/water system.Angewandte Chemie, 43 34
H. Pellissier (2008)
Recent Developments in Dynamic Kinetic ResolutionChemInform, 42
Marina Krausser, W. Hummel, H. Gröger (2007)
Enantioselective one-pot two-step synthesis of hydrophobic allylic alcohols in aqueous medium through the combination of a wittig reaction and an enzymatic ketone reductionEuropean Journal of Organic Chemistry, 2007
J. Longmire, Guoxin Zhu, Xumu Zhang (1997)
ASYMMETRIC ALLYLIC ALKYLATION CATALYZED BY PALLADIUM COMPLEXES WITH A NEW CHIRAL BISPHOSPHINE LIGANDTetrahedron Letters, 38
M. Makkee (1980)
Combined action of enzyme and metal catalyst, applied to the preparation of D-mannitolJournal of The Chemical Society, Chemical Communications
O. Pàmies, J. Bäckvall (2003)
Combination of enzymes and metal catalysts. A powerful approach in asymmetric catalysis.Chemical reviews, 103 8
W. Stampfer, B. Kosjek, C. Moitzi, W. Kroutil, K. Faber (2002)
Biocatalytic asymmetric hydrogen transfer.Angewandte Chemie, 41 6
Two breeds of cat: A palladium‐catalyzed Suzuki cross‐coupling and an enzymatic reduction with an alcohol dehydrogenase from Rhodococcus sp. together enable the efficient and highly enantioselective synthesis of chiral biaryl alcohols in a one‐pot process (see scheme).
Angewandte Chemie International Edition – Wiley
Published: Nov 24, 2008
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