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Issue 0, 1974
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Stable free radicals. Part II. Some substituted pyridinyls

Abstract

Cyano and methoxycarbonyl substituents at the 2- and 6-positions, unlike methyl groups, strongly stabilize pyridinyl radicals, particularly if the 4-position is blocked. The structure–stability relationships in this series afford further evidence for the zwitterionic stabilization of radicals.

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Article type: Paper
DOI: 10.1039/P19740001427
Citation: J. Chem. Soc., Perkin Trans. 1, 1974,0, 1427-1432
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    Stable free radicals. Part II. Some substituted pyridinyls

    A. R. Katritzky and F. Soti, J. Chem. Soc., Perkin Trans. 1, 1974, 0, 1427
    DOI: 10.1039/P19740001427

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