4.8 Article

Cp*Co(III)-Catalyzed Regioselective Synthesis of Cyclopenta[b]carbazoles via Dual C(sp2)-H Functionalization of 1-(Pyridin-2-yl)-indoles with Diynes

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ORGANIC LETTERS
卷 20, 期 24, 页码 7884-7887

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AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.8b03438

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  1. National Natural Science Foundation of China [21672108]
  2. Natural Science Foundation of Tianjin [16JCZDJC31700]

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Cp*Co(III)-catalyzed synthesis of cyclopenta [b-carbazoles from 1-(pyridin-2-yl)-indoles and diynes is developed. This reaction involves dual C-H activation of indoles and domino cyclizations with diynes and has excellent regioselectivity, high efficiency, a broad substrate scope, and tolerance for various functional groups. A series of cyclopenta[b]carbazole molecular scaffolds are obtained in good to excellent yields.

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