Biomimetic Synthesis of Moschamine-Related Indole Alkaloids via Iron-Catalyzed Selectively Oxidative Radical Coupling

Org Lett. 2016 Mar 18;18(6):1474-7. doi: 10.1021/acs.orglett.6b00417. Epub 2016 Mar 7.

Abstract

An iron-catalyzed oxidative radical coupling reaction was developed to selectively construct indolofuran or bisphenolic indole cores, which exist in two types of moschamine-related indole alkaloids. Both (+)-decursivine and 4,4″-bis(N-feruloyl)serotonin were biomimetically synthesized by using coupling reactions. The proposed reassignment of the structure of montamine as 4,4″-bis(N-feruloyl)serotonin was excluded.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomimetics
  • Catalysis
  • Indole Alkaloids / chemical synthesis*
  • Indole Alkaloids / chemistry
  • Iron / chemistry*
  • Molecular Structure
  • Oxidative Coupling
  • Serotonin / analogs & derivatives
  • Stereoisomerism

Substances

  • 4,4'-bis(N-feruloyl)serotonin
  • Indole Alkaloids
  • decursivine
  • Serotonin
  • Iron