Stereospecific microbial oxidation of thioethers to sulfoxides. Application to the synthesis of R-mevalonolactone.-Reference-Cited by-同舟云学术

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Stereospecific microbial oxidation of thioethers to sulfoxides. Application to the synthesis of R-mevalonolactone.

Published:1978-01 Issue:37 Volume:19 Page:3415-3418
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Abushanab Elie,Reed Douglas,Suzuki Fumio,Sih Charles J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference25 articles.

1. Asymmetric Oxidation of Thioethers to Sulfoxides. Configurational Specificity Induced by Optically Active Organic Catalysts1

2. Can circularly polarized light be used to obtain chiral compounds of high optical purity?

3. Organosulfur compounds. 13. Optical resolution of chiral sulfinyl compounds via .beta.-cyclodextrin inclusion complexes

4. THE REACTION BETWEEN ORGANOMAGNESIUM HALIDES AND THE ESTERS OF SOME SULFUR ACIDS

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1. Enzymatic reactions involving the heteroatoms from organic substrates;Anais da Academia Brasileira de Ciências;2018

2. Biocatalytic Applications;Biotransformations in Organic Chemistry;2017-11-28

3. 7.14 Oxidation: Asymmetric Enzymatic Sulfoxidation;Comprehensive Chirality;2012

4. Biocatalytic Applications;Biotransformations in Organic Chemistry;2011

5. Chiral Organosulfur Compounds;Topics in Stereochemistry;2007-02-26

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