Issue 20, 1996

Enantioselective oxidation of sulfides to sulfoxides catalysed by bacterial cyclohexanone monooxygenases

Abstract

This review article briefly introduces the applications of bacterial cyclohexanone monooxygenases to the enantioselective oxidations of organic sulfur compounds to sulfoxides. High enantioselectivities are observed in the sulfoxidation of alkyl aryl sulfides, disulfides, dialkyl sulfides, cyclic and acyclic 1,3-dithioacetals. The oxidation of alkyl aryl sulfides with flavin dependent microorganisms extends the synthetic interest of this class of enzymes.

Article information

Article type
Paper

Chem. Commun., 1996, 2303-2307

Enantioselective oxidation of sulfides to sulfoxides catalysed by bacterial cyclohexanone monooxygenases

S. Colonna, N. Gaggero, P. Pasta and G. Ottolina, Chem. Commun., 1996, 2303 DOI: 10.1039/CC9960002303

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements