Issue 11, 1986

Ready nucleophilic ring opening of β-epoxy-sulphone, -sulphoxide, and -ester with grignard reagents

Abstract

Treatment of β-epoxy-sulphone, -sulphoxide, and -ester with Grignard reagents and copper(I) iodide in diethyl ether–tetrahydrofuran at low temperature leads to rapid ring opening without loss of chirality.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 836-837

Ready nucleophilic ring opening of β-epoxy-sulphone, -sulphoxide, and -ester with grignard reagents

R. Tanikaga, K. Hosoya and A. Kaji, J. Chem. Soc., Chem. Commun., 1986, 836 DOI: 10.1039/C39860000836

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