4.8 Article

Copper-Catalyzed Oxidative Dearomatization/Spirocyclization of Indole-2-Carboxamides: Synthesis of 2-Spiro-pseudoindoxyls

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ORGANIC LETTERS
卷 18, 期 23, 页码 6124-6127

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AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b03131

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  1. National Natural Science Foundation of China [21272074]
  2. Program for Changjiang Scholars and Innovative Research Team in University (PCSIRT)

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A copper-catalyzed oxidative dearomatization/spirocyclization of indole-2-carboxamides using tert-butyl hydro peroxide (TBHP) as the oxidant has been developed that provides rapid and efficient access to C2-spiro-pseudoindoxyls. Two of the sp(2) C-H bonds are functionalized during the reaction process, and the reaction likely proceeds via the formation of a highly reactive 3H-indol-3-one intermediate followed by aromatic electrophilic substitution with the N-aryl ring of the amide moiety.

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