103594-23-6Relevant articles and documents
Experimental evidence for the formation of cationic intermediates during iodine(iii)-mediated oxidative dearomatization of phenols
Tang, Ting,Harned, Andrew M.
, p. 6871 - 6874 (2018/10/02)
Iodine(iii)-based oxidants are commonly used reagents for the oxidative dearomatization of phenols. Having a better understanding of the mechanism through which these reactions proceed is important for designing new iodine(iii)-based reagents, catalysts, and reactions. We have performed a Hammett analysis of the oxidative dearomatization of substituted 4-phenylphenols. This study confirms that iodine(iii)-mediated oxidative dearomatizations likely proceed through cationic phenoxenium ions and not the direct addition of a nucleophile to an iodine-bound phenol intermediate.
ANODIC OXIDATION STUDIES OF OXYGENATED BIPHENYLS. CONVENIENT SYNTHETIC ROUTES TO CERTAIN FUNCTIONALIZED BIPHENYLS
DeSchepper, Richard E.,Swenton, John S.
, p. 4831 - 4834 (2007/10/02)
The anodic oxidation of oxygenated biphenyls produces phenyl-substituted p-quinol ether ketals in good-to-excellent yield.These compounds are useful substrates for preparation of more highly functionalized biphenyls.
