Enzyme directed diastereoselectivity in chemical reductions: studies towards the preparation of all four isomers of 1-phenyl-1,3-butanediol-Reference-Cited by-同舟云学术

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Enzyme directed diastereoselectivity in chemical reductions: studies towards the preparation of all four isomers of 1-phenyl-1,3-butanediol

Published:2004-06 Issue:11 Volume:15 Page:1685-1692
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Ahmad K.,Koul S.,Taneja S.C.,Singh A.P.,Kapoor M.,Riyaz-ul-Hassan ,Verma V.,Qazi G.N.

Publisher

Elsevier BV

Subject

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

Reference27 articles.

1. Recent developments in asymmetric reduction of ketones with biocatalysts

2. Baker's yeast mediated transformations in organic chemistry

3. New approach to regioselective synthesis: Using proteins in vitro as guidance—regioselective reduction of steroids with guidance from bovine serum albumin

4. Stereoselective Syntheses of Building Blocks with Three Consecutive Stereogenic Centers: Important Precursors of Polyketide Natural Products [New Synthetic Methods (68)]

5. Directed reduction of .beta.-hydroxy ketones employing tetramethylammonium triacetoxyborohydride

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4. Secondary metabolites from the marine-derived fungus Paraconiothyrium sp. VK-13;Vietnam Journal of Chemistry;2018-08

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