Issue 15, 1971

Intermediates in aromatic nucleophilic substitution reactions: Meisenheimer complexes from 1-chloro-2,6-dinitro-4-X-benzenes

Abstract

The coloured intermediates initially produced on the addition of sodium methoxide to 1-chloro-2,6-dinitro-4-X-benzenes in dimethyl sulphoxide are shown to result from base addition at a ring carbon carrying hydrogen rather than at the chloro-substituted position.

Article information

Article type
Paper

J. Chem. Soc. D, 1971, 834b-835

Intermediates in aromatic nucleophilic substitution reactions: Meisenheimer complexes from 1-chloro-2,6-dinitro-4-X-benzenes

M. R. Crampton, M. A. El Ghariani and H. A. Khan, J. Chem. Soc. D, 1971, 834b DOI: 10.1039/C2971000834B

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