Highly enantioselective reduction of the C–C double bond of N-phenyl-2-methyl- and N-phenyl-2,3-dimethyl- maleimides by fungal strains-Reference-Cited by-同舟云学术

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Highly enantioselective reduction of the C–C double bond of N-phenyl-2-methyl- and N-phenyl-2,3-dimethyl- maleimides by fungal strains

Published:2009-06 Issue:10 Volume:20 Page:1106-1108
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Sortino Maximiliano A.,Filho Valdir Cechinel,Zacchino Susana A.

Publisher

Elsevier BV

Subject

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

Reference15 articles.

1. Fungal Bioconversions: Applications to the Manufacture of Pharmaceuticals;Chartrain,2005

2. Novel bioreduction system for the production of chiral alcohols

3. Differences in bioactivity between the enantiomers of α-pinene and limonene

4. The enantiomers of the teratogenic thalidomide analogue EM 12

5. R-(+)- andS-(−)-carvone: influence of chirality on locomotion activity in mice

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