Issue 7, 1982

Brönsted and Lewis acid catalysis of X[double bond, length half m-dash]Y–ZH cycloadditions

Abstract

Cycloadditions of arylidene imdines of methyl phenylglycinate show substantial rate enhancement in the presence of Brönsted and Lewis acids; for Brönsted acids the rate is related to the pKa of the acid, whilst for the Lewis acids studied the rate acceleration decreased in the order Zn(OAc)2 > AgOAc > LiOAc > Mg(OAc)2.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1982, 384-386

Brönsted and Lewis acid catalysis of X[double bond, length half m-dash]Y–ZH cycloadditions

R. Grigg and H. Q. N. Gunaratne, J. Chem. Soc., Chem. Commun., 1982, 384 DOI: 10.1039/C39820000384

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