Copper-mediated chemoselective trifluoromethylation at the benzylic position by the use of shelf-stable electrophilic trifluoromethylating reagents 3 in good to high yields under mild conditions is described for the first time. The generality of this trifluoromethylation for a wide variety of benzyl bromides facilitates the rapid creation of structural diversity of medicinal candidates in drug discovery.
Org. Lett., 2011, 13 (14), pp 3596–3599
DOI: 10.1021/ol201205t
https://pubs.acs.org/doi/abs/10.1021/ol201205t
标签: 三氟甲基
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