@article{oai:nagoya.repo.nii.ac.jp:00024636,
 author = {Yamamoto, Yoshihiko and Ohkubo, Erina and Shibuya, Masatoshi},
 issue = {10},
 journal = {ADVANCED SYNTHESIS & CATALYSIS},
 month = {May},
 note = {The copper-catalyzed hydroarylation of (trifluoromethyl)alkynes with (o-nitrophenyl)boronic acids selectively afforded trisubstituted (trifluoromethyl)alkenes bearing an o-nitrophenyl group. The obtained hydroarylation products were converted into 3-aryl-2-(trifluoromethyl)indoles in high yields via molybdenum-catalyzed Cadogan cyclization. Similarly, the hydroarylation product prepared from (o-nitrophenyl)(trifluoromethyl)alkyne and (p-anisyl)boronic acid also underwent Cadogan cyclization, albeit with a longer reaction time, affording the desired indole product in a high yield.},
 pages = {1747--1751},
 title = {Synthesis of 3-Aryl-2-(trifluoromethyl)indoles via Copper-Catalyzed Hydroarylation and Subsequent Cadogan Cyclization},
 volume = {359},
 year = {2017}
}