Issue 4, 1974

The kinetics and mechanism of the electrophilic substitution of heteroaromatic compounds. Part XXXVI. The nitration of some 1-phenylpyrazoles

Abstract

The kinetics of nitration of 1-phenylpyrazole and its 4- and 4′-nitro-derivatives, and the corresponding 2-methyl quaternary salts are used to elucidate the species which undergo nitration. The nitration rates are compared within the series and with those of other heteroaromatic compounds.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1974, 389-394

The kinetics and mechanism of the electrophilic substitution of heteroaromatic compounds. Part XXXVI. The nitration of some 1-phenylpyrazoles

A. G. Burton, A. R. Katritzky, M. Konya and H. O. Tarhan, J. Chem. Soc., Perkin Trans. 2, 1974, 389 DOI: 10.1039/P29740000389

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