Nucleophilic character of the alkyl radicals. 19. 1a Absolute rate constants in the homolytic alkylation of protonated heteroaromatic bases by n-butyl and tert-butyl …
A Citterio, F Minisci, V Franchi
Index: Citterio, Attilio; Minisci, Francesco; Franchi, Valeria Journal of Organic Chemistry, 1980 , vol. 45, # 23 p. 4752 - 4757
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Citation Number: 43
Abstract
The rate constants for the homolytic alkylation of protonated heteroaromatic bases (quinoline, pyridine, and 4-cyano-, 4-acetyl-, 4-methyl-, and 4-methoxypyridine) by n-butyl and tert-butyl radicals were measured at 57 “C by competition of the aromatic addition with the alkyl radical oxidation by Cu2+ salts (for which the rates are known). With the more activated substrates (quinoline and 4-cyano-and 4-acetylpyridine) the tert-butyl radical is ...
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