Issue 11, 1980

Studies on decarboxylation reactions. Part 4. Kinetic study of the decarboxylation of some N-alkyl- or N-phenyl-substituted 5-amino-1,3,4-oxadiazole-2-carboxylic acids

Abstract

The rate constants of the decarboxylation reaction of compounds (Ib–f) have been measured in water over a range of proton activities, at various temperatures. The results obtained strongly support the unimolecular decarboxyprotonation mechanism.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1980, 1627-1630

Studies on decarboxylation reactions. Part 4. Kinetic study of the decarboxylation of some N-alkyl- or N-phenyl-substituted 5-amino-1,3,4-oxadiazole-2-carboxylic acids

R. Noto, F. Buccheri, G. Consiglio and D. Spinelli, J. Chem. Soc., Perkin Trans. 2, 1980, 1627 DOI: 10.1039/P29800001627

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