Issue 10, 1994

Aromatic nucleophilic substitution reactions of some 2-L-3-nitro-5-X-thiophenes with piperidine and aniline in methanol. Substituent constants for the thiophene system

Abstract

The rate constants for the reactions of some 2-L-3-nitro-5-X-thiophenes 14 with aniline and of compounds (4) with piperidine in methanol have been measured at various temperatures. By using the data obtained in this work as well as previously available data sets, a series of optimized ‘thiophene’σT values has been calculated. The susceptibility constants ρ(L)of the various sets have been analysed in the framework of the reactivity–selectivity principle.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1994, 2187-2189

Aromatic nucleophilic substitution reactions of some 2-L-3-nitro-5-X-thiophenes with piperidine and aniline in methanol. Substituent constants for the thiophene system

G. Consiglio, V. Frenna, C. Arnone, E. Mezzina and D. Spinelli, J. Chem. Soc., Perkin Trans. 2, 1994, 2187 DOI: 10.1039/P29940002187

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