A copper-catalyzed tandem radical cyclization of 1-(3-phenylprop-2-yn-1-yl)-1 H -indole with diphenylphosphine oxides was developed. C–P bond formation was achieved coupled with C(sp 2 )–H functionalization. It provided an access to construct the pyrrolo[1,2- a ]indole motif and a series of 2-phosphinoyl-9 H -pyrrolo[1,2- a ]indoles.
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Zhang et al. (2017) studied this question.
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