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

Ying-Ying HeXiao-Xue SunGuo-Hao LiGuang-Jian MeiFeng Shi
Published in: The Journal of organic chemistry (2017)
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.
Keyphrases
  • anaerobic digestion
  • ionic liquid
  • structural basis
  • carbon dioxide
  • structure activity relationship
  • amino acid
  • crystal structure