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Catalyst-Controlled Diastereoselective Synthesis of Bridged [3.3.1] Bis(Indolyl)-Oxanes and Oxepanes via Desymmetrization of Bis(Indolyl)-Cyclohexadienones.

Abhishek Kumar MishraAnil ChauhanSantosh KumarRuchir KantRavindra Kumar
Published in: Organic letters (2023)
A catalyst-controlled divergent synthesis of bridged [3.3.1] bis(indolyl)-oxanes and cis -[6.7] fused bis(indolyl) oxepanes via diastereoselective desymmetrization of bis(indolyl)-cyclohexadienones is presented for the first time. The reaction is highly atom- and step-economic, furnishing sp 3 -rich functionalized bis(indolyl) derivatives in good to excellent yields with wide substrate scope. The reaction proceeds through Friedel-Crafts alkylation followed by catalyst-controlled selective C-C bond formation/rearrangement. Gram scale synthesis and synthetic utility to generate bis(indolyl) alkaloid-like molecular diversity were also illustrated.
Keyphrases
  • ionic liquid
  • room temperature
  • highly efficient
  • reduced graphene oxide
  • tandem mass spectrometry
  • simultaneous determination