4.7 Article

Substrate-Controlled Regioselective Arylations of 2-Indolylmethanols with Indoles: Synthesis of Bis(indolyl)methane and 3,3'-Bisindole Derivatives

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JOURNAL OF ORGANIC CHEMISTRY
卷 82, 期 5, 页码 2462-2471

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AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.6b02850

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资金

  1. National Natural Science Foundation of China [21372002, 21232007]
  2. PAPD
  3. TAPP
  4. Natural Science Foundation of Jiangsu Province [BK20160003]

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A substrate-controlled regioselective arylation of 2-indolylmethanols with indoles has been established, which efficiently afforded bis(indolyl)methane and 3,3'-bisindole derivatives in high yields and with a broad substrate scope (up to 98% yield, 36 examples). This approach will not only provide an important strategy for the diversified synthesis of bis(indolyl)methane and 3,3'-bisindole derivatives but also serve as a good example for substrate-controlled regioselective reactions.

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