Synthesis of di(hetero)aryl sulfides by defluorinative sulfenylation of polyfluoroalkyl ketones with sodium sulfinates or arylsulfonyl chlorides?
Chemical Communications Pub Date: 2020-06-22 DOI: 10.1039/D0CC03303K
Abstract
A facile incorporation of a privileged sulfide, a naphthofuran framework, and a perfluoroalkyl moiety in one molecule was successfully accomplished through tandem defluorinative sulfenylation of α-perfluoroalkyl ketones with a sulfur source. The reaction presumably proceeds via a sequence involving defluorination, reductive sulfenylation, autoaromatization, and annulation, accompanied by the simultaneous cleavage of four C(sp3)–F bonds and the formation of new C–S and C–O bonds.
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Journal Name：Chemical Communications
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CAS no.: 89640-58-4
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