4.8 Article

Rhodium-Catalyzed Coupling-Cyclization of Alkenyldiazoacetates with o-Alkenyl Arylisocyanides: A General Route to Carbazoles

Journal

ORGANIC LETTERS
Volume 21, Issue 9, Pages 2973-2977

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b00307

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Funding

  1. National Natural Sciences Foundation of China [21871044, 21472017]
  2. Natural Sciences Foundation of Jilin Province [20190201073JC]

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A rhodium-catalyzed coupling-cyclization reaction of alkenyldiazoacetates with o-alkenyl arylisocyanides has been developed. In this reaction, the highly reactive alkenylketenimine intermediates generated by coupling reaction of alkenyldiazoacetates with o-alkenyl arylisocyanides undergo intramolecular [4 + 2] cycloaddition and provide a novel, highly efficient method for the one-step synthesis of carbazoles by formation of three new bonds and two rings from readily available acyclic starting materials.

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