Issue 23, 1985

A new enantioselective asymmetric synthesis of alkyl t-butylsulphinates

Abstract

The reaction of symmetrical sulphites with t-butylmagnesium chloride in the presence of chiral aminoalcohols has been found to proceed in an asymmetric way affording chiral t-butylsulphinates in 40–70% enantiomeric excess.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 1670-1672

A new enantioselective asymmetric synthesis of alkyl t-butylsulphinates

J. Drabowicz, S. Legedź and M. Mikołajczyk, J. Chem. Soc., Chem. Commun., 1985, 1670 DOI: 10.1039/C39850001670

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.

Spotlight

Advertisements