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首页> 外文期刊>ACS catalysis >From Indoles to Carbazoles: Tandem Cp~*Rh(III)-Catalyzed C-H Activation/Bronsted Acid-Catalyzed Cyclization Reactions
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From Indoles to Carbazoles: Tandem Cp~*Rh(III)-Catalyzed C-H Activation/Bronsted Acid-Catalyzed Cyclization Reactions

机译:从讽刺到咔唑:串联CP〜* RH(III) - 催化C-H催化/铜架催化环化反应

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摘要

A tandem Cp~*Rh(III)-catalyzed C-H activation/Bronsted acid-catalyzed intramolecular cyclization allows a facile synthesis of carbazoles from readily available indoles. The reaction proceeds under rather mild reaction conditions with the generation of water and N2 as the only byproducts. Broad substrate scope, excellent functional group tolerance, and high yields were observed. The benzannulation of pyroles for the synthesis of indoles is also feasible using the same protocol.
机译:串联CP〜* RH(III) - 催化的C-H抗激活/抗正酸催化的分子内环化允许从容易获得的吲哚进行容易合成咔唑。 反应在相当温和的反应条件下进行,用水和N 2作为唯一的副产物。 宽底物范围,优异的官能团耐受性和高收率。 使用相同的协议,用于合成吲哚的热源的Benzulation也是可行的。

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