Microbiological Transformations 43. Epoxide Hydrolases as Tools for the Synthesis of Enantiopure α-Methylstyrene Oxides: A New and Efficient Synthesis of (S)-Ibuprofen-Reference-Cited by-同舟云学术

Microbiological Transformations 43. Epoxide Hydrolases as Tools for the Synthesis of Enantiopure α-Methylstyrene Oxides: A New and Efficient Synthesis of (S)-Ibuprofen

Published:1999-06-24 Issue:14 Volume:64 Page:5029-5035
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Cleij M.¹,Archelas A.¹,Furstoss R.¹

Affiliation:

1. Groupe Biocatalyse et Chimie Fine, ESA 6111 associée au CNRS, Faculté des Sciences de Luminy, Université de la Méditerranée, Case 901, 163 avenue de Luminy, 13288 Marseille Cedex 9, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo982101%2B

Reference43 articles.

1. (a) Brandes, B. D.; Jacobsen, E. N.Tetrahedron: Asymmetry1997,8, 3927.

2. Catalytic asymmetric oxidations using optically active (salen)manganese(III) complexes as catalysts

3. Enantioselective catalytic ring opening of epoxides with carboxylic acids

4. Catalytic Asymmetric Dihydroxylation

5. Microbial Epoxide Hydrolases.

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