Issue 19, 1993

Atropisomer-selective 1,1-binapthyl synthesis via chirality transfer from sulfur

Abstract

4,5-Dihydro-2-(1-alkyl- or 1-aryl-sulfinylnaphthalen-2-yl)-4,4-dimethyloxazoles 36 undergo substitution reactions on treatment with Grignard reagents; the optically active sulfoxide 14 on treatment with 1-naphthylmagnesium bromide furnished the 1,1-binaphthyl 15 in 60% enantiomeric excess (e.e.).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1993, 1489-1491

Atropisomer-selective 1,1-binapthyl synthesis via chirality transfer from sulfur

R. W. Baker, G. R. Pocock and M. V. Sargent, J. Chem. Soc., Chem. Commun., 1993, 1489 DOI: 10.1039/C39930001489

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