Issue 9, 2002

The in situoxidation–Wittig reaction of α-hydroxyketones

Abstract

In situ oxidation–Wittig methodology has been applied to α-hydroxyketones avoiding the problems normally associated with α-ketoaldehydes; the procedure is practically simple, and in many cases gives high yields of the product γ-ketocrotonates; the procedure has also been successfully utilised with ethyl glycolate and glycolaldehyde dimer.

Graphical abstract: The in situ oxidation–Wittig reaction of α-hydroxyketones

Article information

Article type
Communication
Submitted
11 Feb 2002
Accepted
28 Feb 2002
First published
04 Apr 2002

Chem. Commun., 2002, 974-975

The in situ oxidationWittig reaction of α-hydroxyketones

K. A. Runcie and R. J. K. Taylor, Chem. Commun., 2002, 974 DOI: 10.1039/B201513G

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.

Social activity

Spotlight

Advertisements