Issue 5, 1991

First example of epibromohydrin as an acetone equivalent

Abstract

In the presence of lithium diisopropylamide at low temperature, the anion of the amino nitrile 1 is alkylated with epibromohydrin to give an acetonyl derivative 3; allene oxide is invoked as the reactive intermediate.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1991, 1346-1347

First example of epibromohydrin as an acetone equivalent

F. Vergne, D. J. Aitken and H. Husson, J. Chem. Soc., Perkin Trans. 1, 1991, 1346 DOI: 10.1039/P19910001346

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