Issue 2, 1973

Cyanosilylation of aldehydes and ketones. A convenient route to cyanohydrin derivatives

Abstract

A wide variety of aldehydes and ketones reacts with trimethylsilyl cyanide under both thermal and catalytic conditions to give α-silyloxy nitriles which may be useful intermediates and protective groups in organic synthesis.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1973, 55-56

Cyanosilylation of aldehydes and ketones. A convenient route to cyanohydrin derivatives

D. A. Evans, L. K. Truesdale and G. L. Carroll, J. Chem. Soc., Chem. Commun., 1973, 55 DOI: 10.1039/C39730000055

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