A. Ikeda, M. Omote, K. Kusumoto, M. Komori, A. Tarui, K. Sato and A. Ando
Org. Biomol. Chem., 2016,14, 2127-2133
DOI:
10.1039/C5OB02558C,
Paper
The addition of InBr3 to the oxidative Sonogashira cross-coupling reaction of 2-ethynylaniline with (E)-trimethyl(3,3,3-trifluoroprop-1-enyl)silane led to a dramatic increase in the reactivity to afford the corresponding 1,3-enynes bearing a trifluoromethyl group on their terminal sp2 carbon. The subsequent cyclization of these 1,3-enynes under palladium catalysis provides access to the corresponding indoles bearing a 3,3,3-trifluoroprop-1-enyl group at their 2-position.