Rhodium(III)-Catalyzed C-H Alkenylation: Access to Maleimide-Decorated Tryptophan and Tryptophan-Containing Peptides

Org Lett. 2020 Feb 21;22(4):1535-1541. doi: 10.1021/acs.orglett.0c00086. Epub 2020 Feb 3.

Abstract

Maleimide is widely applied in many fields, especially in antibody-drug conjugations and peptide drugs. Herein, we develop a strategy for the C-H alkenylation of tryptophan and tryptophan-containing peptides, providing a synthetic route of decorating maleimide on peptides. The method has a high tolerance of functional groups and protecting groups. Furthermore, this method was applied to prepare peptide conjugation with molecules such as drugs and fluorescence probes. Moreover, macrocyclic peptides were obtained via this reaction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkenes / chemistry*
  • Catalysis
  • Maleimides / chemical synthesis*
  • Maleimides / chemistry
  • Molecular Structure
  • Peptides / chemical synthesis*
  • Peptides / chemistry
  • Rhodium / chemistry*
  • Tryptophan / chemical synthesis*
  • Tryptophan / chemistry

Substances

  • Alkenes
  • Maleimides
  • Peptides
  • maleimide
  • Tryptophan
  • Rhodium