4.7 Article

Synthesis of Trifluoromethyl- and Ester Group-Substituted α-Carbolines via Iron-Catalyzed Tandem Cyclization Reaction

期刊

JOURNAL OF ORGANIC CHEMISTRY
卷 85, 期 6, 页码 4354-4364

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.0c00048

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资金

  1. Natural Science Foundation of China [21402068, 21502075, 21762018]
  2. Natural Science Foundation of Jiangxi Province [20192BCBL23009]
  3. Open Project Program of Key Laboratory of Functional Small Organic Molecule, Ministry of Education, Jiangxi Normal University [KLFS-KF-201406]

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An efficient approach to prepare trifluoromethyl-alpha-carbolines and ester group-substituted alpha-carbolines via the tandem cyclization reaction of 2-(2-aminophenyl)acetonitriles and trifluoromethyl 1,3-diones or beta,gamma-unsaturated alpha-ketoesters was reported. The transformation proceeded smoothly in the presence of catalytic environmental-benign iron salts, which are used to prepare the desired products in moderate to good yields.

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