Nickel-catalyzed and benzoic acid-promoted direct sulfenylation of unactivated arenes
Chemical Communications2015Vol. 51(17), pp. 3582–3585
Citations Over TimeTop 10% of 2015 papers
Abstract
A nickel-catalyzed and benzoic acid-promoted direct sulfenylation of unactivated arenes using removable 2-(pyridine-2-yl)-isopropylamine as a directing group is described. This strategy provides an efficient access to valuable aryl sulfides with ample substrate scope and a high degree of functional group tolerance.
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