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Merck

Nickel-catalyzed synthesis of diarylsulfides and sulfones via C-H bond functionalization of arylamides.

Organic & biomolecular chemistry (2015-05-27)
Vutukuri Prakash Reddy, Renhua Qiu, Takanori Iwasaki, Nobuaki Kambe
RESUMEN

The direct sulfenylation and sulfonylation of (sp(2))C-H bonds of benzamide derivatives were achieved using a Ni catalyst with the aid of an 8-aminoquinoline moiety as a bidentate directing group. These protocols represent a convenient route for the formation of valuable diaryl sulfides and sulfones in moderate to excellent yields.

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Sigma-Aldrich
8-Aminoquinoline, 98%
Sigma-Aldrich
Benzoyl chloride, 99%
Sigma-Aldrich
Benzoyl chloride, ReagentPlus®, ≥99%
Sigma-Aldrich
Benzoyl chloride, SAJ first grade, ≥98.0%