Issue 2, 1984
From the journal:

Journal of the Chemical Society, Perkin Transactions 2

Electrophilic ipso-substitutions. Part 3. Reactions of 3-substituted indoles,4-substituted N,N-dimethylanilines, and 1- and 3-substituted indolizines with nitrous acid

Martino Colonna,   Lucedio Greci  and  Marino Poloni  

Abstract

Reactions of 3-substituted indoles, N,N-dimethylanilines, and 1- and 3-substituted indolizines with nitrous acid yield products of ipso-substitutions, essentially the corresponding nitro-derivatives. An electron transfer process is proposed for the initial step, on the basis of reaction products, e.s.r. evidence, and substrate oxidation potentials.

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Article information

DOI
https://doi.org/10.1039/P29840000165
Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1984, 165-169

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Electrophilic ipso-substitutions. Part 3. Reactions of 3-substituted indoles,4-substituted N,N-dimethylanilines, and 1- and 3-substituted indolizines with nitrous acid

M. Colonna, L. Greci and M. Poloni, J. Chem. Soc., Perkin Trans. 2, 1984, 165 DOI: 10.1039/P29840000165

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