Stereoselective anti-Prelog reduction of ketones by whole cells of Comamonas testosteroni in a ‘substrate-coupled’ approach-Reference-Cited by-同舟云学术

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Stereoselective anti-Prelog reduction of ketones by whole cells of Comamonas testosteroni in a ‘substrate-coupled’ approach

Published:2008-11 Issue:3-4 Volume:55 Page:126-129
ISSN:1381-1177
Container-title:Journal of Molecular Catalysis B: Enzymatic
language:en
Short-container-title:Journal of Molecular Catalysis B: Enzymatic

Author:

Wallner Sabine R.,Lavandera Iván,Mayer Sandra F.,Öhrlein Reinhold,Hafner Andreas,Edegger Klaus,Faber Kurt,Kroutil Wolfgang

Publisher

Elsevier BV

Subject

Process Chemistry and Technology,Biochemistry,Bioengineering,Catalysis

Reference58 articles.

1. KUR-1246, a novel β2-adrenoceptor agonist, as a tocolytic agent

2. The Practical Synthesis of a Uterine Relaxant, Bis(2-{[(2S)-2-({(2R)-2-hydroxy-2-[4-hydroxy-3-(2-hydroxyethyl)-phenyl]ethyl}amino)-1,2,3,4-tetrahydronaphthalen-7-yl]oxy}-N,N-dimethylacetamide) Sulfate (KUR-1246).

3. Chemoenzymatic synthesis of (R)- and (S)-tembamide, aegeline and denopamine by a one-pot lipase resolution protocol

4. Enantioselective addition of diorganozincs to aldehydes catalyzed by β-amino alcohols

5. Chemo-enzymatic synthesis of the active enantiomer of the anorressant 2-benzylmorpholine

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