Enantioselective One-Pot Two-Step Synthesis of Hydrophobic Allylic Alcohols in Aqueous Medium through the Combination of a Wittig Reaction and an Enzymatic Ketone Reduction-Reference-Cited by-同舟云学术

Enantioselective One-Pot Two-Step Synthesis of Hydrophobic Allylic Alcohols in Aqueous Medium through the Combination of a Wittig Reaction and an Enzymatic Ketone Reduction

Published:2007-11 Issue:31 Volume:2007 Page:5175-5179
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Kraußer Marina,Hummel Werner,Gröger Harald

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference39 articles.

1. Novel bioreduction system for the production of chiral alcohols

2. H. Gröger in Biocatalysis in the Pharmaceutical and Biotechnology Industries (Ed.: , CRC Press, New York, 2006 , , pp. 757–790.

3. Highly Regio- and Enantioselective Reduction of 3,5-Dioxocarboxylates

4. Synthesis of optically pure ethyl ( S )-4-chloro-3-hydroxybutanoate by Escherichia coli transformant cells coexpressing the carbonyl reductase and glucose dehydrogenase genes

5. Practical Application of Recombinant Whole-Cell Biocatalysts for the Manufacturing of Pharmaceutical Intermediates Such as Chiral Alcohols

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