Issue 2, 2000
From the journal:

Mendeleev Communications

The differing reactivity of the bromo and nitro groups in 4-bromo-5-nitrophthalonitrile towards nucleophilic attack

Igor G. Abramov,   Mikhail V. Dorogov,   Sergei A. Ivanovskii,   Alexei V. Smirnov  and  Marina B. Abramova  

Abstract

The high reactivity of 4-bromo-5-nitrophthalonitrile and different mobilities of the leaving groups (bromo and nitro) in aromatic nucleophilic substitution reactions offer new opportunities for the synthesis of substituted phthalonitriles and then various hetero-cyclic compounds.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1070/MC2000v010n02ABEH001147
Article type
Paper

Mendeleev Commun., 2000,10, 78-80

Permissions

Request permissions

The differing reactivity of the bromo and nitro groups in 4-bromo-5-nitrophthalonitrile towards nucleophilic attack

I. G. Abramov, M. V. Dorogov, S. A. Ivanovskii, A. V. Smirnov and M. B. Abramova, Mendeleev Commun., 2000, 10, 78 DOI: 10.1070/MC2000v010n02ABEH001147

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