4.8 Article

Phosphine-Catalyzed Divergent [4+3] Domino Annulations of CF3-Containing Imines with MBH Carbonates: Construction of Perfluoroalkylated Benzazepines

Journal

ORGANIC LETTERS
Volume 21, Issue 17, Pages 7060-7064

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b02626

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Funding

  1. National Natural Science Foundation of China [21672109, 21871148, 21472097]
  2. Natural Science Foundation of Tianjin [15JCYBJC20000]

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Phosphine-catalyzed divergent [4+3] domino annulations of fluorinated imidoyl chlorides with MBH carbonates were developed. Two classes of perfluoroalkylated benzazepines were obtained in moderate to good yields via an interesting dearomatization/rearomatization sequence. Remarkably, the fluorinated imidoyl chlorides could be utilized for the first time as a new four-atom building block in phosphine catalysis. Moreover, the proposed mechanism is supported by capturing the intermediate.

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