4.7 Article

Access to [4,3,1]-Bridged Carbocycles via Rhodium(III)-Catalyzed C-H Activation of 2-Arylindoles and Annulation with Quinone Monoacetals

期刊

JOURNAL OF ORGANIC CHEMISTRY
卷 85, 期 6, 页码 4543-4552

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.0c00018

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资金

  1. NSFC [21525208]
  2. China Postdoctoral Science Foundation [2019TQ0192, 2019M653531, 2019M663613]
  3. Fundamental Research Funds for the Central Universities [GK201903028]
  4. SNNU
  5. National Training Program of Innovation and Entrepreneurship for Undergraduates [CX2019106]

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Reported herein is the Rh(III)-catalyzed annulation of N-unprotected 2-arylindoles with quinone monoacetals for the straightforward synthesis of [4,3,1]-bridged carbocycles with exclusive C(3) selectivity. Mechanistic studies, particularly deuterium-labeling experiments, suggest that the coupling likely proceeds via two-fold C-H activation with two-fold migratory insertion into the enone moieties.

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