Asymmetric reduction of ketones via whole cell bioconversions and transfer hydrogenation: complementary approaches-Reference-Cited by-同舟云学术

Asymmetric reduction of ketones via whole cell bioconversions and transfer hydrogenation: complementary approaches

Published:2001-05 Issue:7 Volume:12 Page:1025-1034
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Hage Annemarie,Petra Daniëlle G.I,Field Jim A,Schipper Dick,Wijnberg Joannes B.P.A,Kamer Paul C.J,Reek Joost N.H,van Leeuwen Piet W.N.M,Wever Ron,Schoemaker Hans E

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference33 articles.

1. Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implications

2. Reduction of Carbonyl Compounds with Chiral Oxazaborolidine Catalysts: A New Paradigm for Enantioselective Catalysis and a Powerful New Synthetic Method

3. Baker's yeast mediated transformations in organic chemistry

4. Synthesis of functionalized chiral synthons via microbiological reduction

5. Homochiral fluoro-organic compounds. Synthesis of the two enantiomers of (Z)-3-fluoro-4-phenyl-1-(p-tolylsulphonyl)but-3-en-2-ol through microbial reduction

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