Cp*CoIII -catalyzed directed C-H trifluoromethylthiolation of 2-phenylpyridines and 6-arylpurines

Chemical Communications : Chem Comm
Misaki YoshidaShigeki Matsunaga

Abstract

Cp*CoIII-catalyzed directed C-H trifluoromethylthiolation using N-trifluoromethylthiodibenzenesulfonimide as an electrophilic SCF3 source is described. 6-Arylpurines, an important structural motif in medicinal chemistry, and 2-phenylpyridines selectively afforded mono-trifluoromethylthiolated products in moderate to good yields using an inexpensive first-row transition metal catalyst.

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Nov 21, 2019·Organic & Biomolecular Chemistry·Alessio BaccaliniDebabrata Maiti
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Jul 25, 2019·The Journal of Organic Chemistry·Yi JiangZhen Wang

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