4.8 Article

An Oxidant-Free Strategy for Indole Synthesis via Intramolecular C-C Bond Construction under Visible Light Irradiation: Cross-Coupling Hydrogen Evolution Reaction

期刊

ACS CATALYSIS
卷 6, 期 7, 页码 4635-4639

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.6b00917

关键词

C-H functionalization; indoles; radical addition; cross-coupling hydrogen evolution; photochemistry

资金

  1. Ministry of Science and Technology of China [2013CB834804, 2014CB239402, 2013CB834505]
  2. National Natural Science Foundation of China [21390404, 91427303, 21402217]
  3. Key Research Programme of the Chinese Academy of Sciences [XDB17030201]
  4. Chinese Academy of Sciences

向作者/读者索取更多资源

We describe here an oxidant-free strategy to synthesize indoles, i.e., under visible-light irradiation (lambda = 450 nm), catalytic amounts of an iridium(III) photosensitizer and cobaloxime catalyst transform various N-aryl enamines exclusively into indoles. Our methodology affords indoles in good to excellent yields under mild reaction conditions and produces H-2 as the only byproduct. Spectroscopic and electrochemical studies verify that the designed system proceeds via visible-light-catalyzed oxidation of N-aryl enamines, followed by intramolecular radical addition to yield the indoles smoothly under ambient conditions.

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