Facile biocatalytic reduction of the carbon–carbon double bond of 5-benzylidenethiazolidine-2,4-diones. Synthesis of (±)-5-(4-{2-[methyl(2-pyridyl)amino]ethoxy}benzyl)thiazolidine-2,4-dione (BRL 49653), its (R)-(+)-enantiomer and analogues-Reference-Cited by-同舟云学术

Facile biocatalytic reduction of the carbon–carbon double bond of 5-benzylidenethiazolidine-2,4-diones. Synthesis of (±)-5-(4-{2-[methyl(2-pyridyl)amino]ethoxy}benzyl)thiazolidine-2,4-dione (BRL 49653), its (R)-(+)-enantiomer and analogues

Published:1994 Issue:22 Volume: Page:3319-3324
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Cantello Barrie C. C.,Eggleston Drake S.,Haigh David,Haltiwanger R. Curtis,Heath Catherine M.,Hindley Richard M.,Jennings Keith R.,Sime John T.,Woroniecki Stefan R.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1994/P1/P19940003319

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1. Asymmetric reduction of nitro olefins by fermenting bakers' yeast

2. Asymmetric reduction of the prochiral carbon-carbon double bond of methyl 2-chloro-2-alkenoates by use of fermenting bakers' yeast

3. 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

4. Asymmetric Reduction of α-Methylene Ketones by Using Fermenting Baker’s Yeast. Preparation of Optically Active β-Hydroxy α-Methyl Ketones

5. Synthesis by microbial reduction of (S)-13-hydroxy-9Z,11E-octadecadienoic acid, a defensive substance in rice.

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