Issue 7, 1970

Stereochemistry of reduction of epoxides by borohydride anion

Abstract

The reduction of an epoxide by borohydride anion is shown to be a stereospecifically trans process by comparison of the [2-2H1] cyclopentanols produced by aluminodeuteride and borodeuteride reduction of cyclopentene oxide.

Article information

Article type
Paper

J. Chem. Soc. C, 1970, 928-928

Stereochemistry of reduction of epoxides by borohydride anion

R. H. Cornforth, J. Chem. Soc. C, 1970, 928 DOI: 10.1039/J39700000928

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