Asymmetric direduction of 1,2-indanedione to cis (1S,2R) indanediol by Trichosporon cutaneum MY 1506-Reference-Cited by-同舟云学术

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Asymmetric direduction of 1,2-indanedione to cis (1S,2R) indanediol by Trichosporon cutaneum MY 1506

Published:1999-01 Issue:5 Volume:88 Page:495-499
ISSN:1389-1723
Container-title:Journal of Bioscience and Bioengineering
language:en
Short-container-title:Journal of Bioscience and Bioengineering

Author:

Stahl Sarah,Ikemoto Norihiro,King Anthony,Greasham Randolph,Chartrain Michel

Publisher

Elsevier BV

Subject

Applied Microbiology and Biotechnology,Bioengineering,Biotechnology

Reference23 articles.

1. Chiral drugs;Stinson,1994

2. Baker's yeast as a reagent in organic synthesis;Servi;Synthesis,1990

3. Enzymes in organic synthesis;Jones;Tetrahedron,1986

4. Advances in biotransformation processes;Lilly;Chem. Eng. Sci.,1994

5. Reductive biotransformations of organic compounds by cells or enzymes of yeast;Ward;Enz. Microbiol. Technol.,1990

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Biocatalytic routes to anti-viral agents and their synthetic intermediates;Chemical Society Reviews;2021

2. 1,2-Indanedione;Encyclopedia of Reagents for Organic Synthesis;2009-03-15

3. Protection of the carbonyl groups in 1,2-indanedione: propellane versus acetal formation;Tetrahedron Letters;2008-03

4. Diplogelasinospora grovesii IMI 171018, a new whole cell biocatalyst for the stereoselective reduction of ketones;Tetrahedron: Asymmetry;2004-03

5. Homochiral (1S,2R)-1,2-indandiol from asymmetric reduction of 1,2-indanedione by resting cells of the yeast Trichosporon cutaneum;Tetrahedron: Asymmetry;2003-08

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