Chemoenzymatic synthesis of enantiopure isopropyl (3R)- and (3S)-3-hydroxycyclohex-1-ene-1-carboxylates and their reduction to isomers of isopropyl 3-hydroxy-cyclohexane-1-carboxylate-Reference-Cited by-同舟云学术

Chemoenzymatic synthesis of enantiopure isopropyl (3R)- and (3S)-3-hydroxycyclohex-1-ene-1-carboxylates and their reduction to isomers of isopropyl 3-hydroxy-cyclohexane-1-carboxylate

Published:2002-04 Issue:6 Volume:13 Page:579-585
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Fonteneau Laure,Rosa Sandra,Buisson Didier

Publisher

Elsevier BV

Subject

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

Reference22 articles.

1. Reduction of 1,1-dideuterio-2-methyl-2-penten-1-ol by beauveria sulfurescens. Mechanism of the microbiological reduction of α,β-unsaturated ald

2. Reduction microbiologique d'aldehydes α, β-ethyleniques par Beauveria sulfurescens

3. Reductions microbiologioues de cetones ethyleniques

4. Microbiological reduction of .alpha.,.beta.-unsaturated ketones by Beauveria sulfurescens

5. Reduction of .ALPHA.,.BETA.-unsaturated ketones by various fungi.

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2. Enantioselective, Biocatalytic Reduction of 3-Substituted Cyclopentenones: Application to the Asymmetric Synthesis of an hNK-1 Receptor Antagonist;Organic Letters;2011-02-08

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