Issue 2, 1987

A short, general, organoselenium-mediated synthesis of cyclic acetals

Abstract

Readily available substrates containing a strategically placed carbonyl group and two isolated double bonds can be coaxed into cyclic acetal formation in a single step employing phenylselenenyl chloride in aqueous acetonitrile.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1987, 78-80

A short, general, organoselenium-mediated synthesis of cyclic acetals

G. Mehta, H. S. P. Rao and K. R. Reddy, J. Chem. Soc., Chem. Commun., 1987, 78 DOI: 10.1039/C39870000078

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