Total Synthesis of Seongsanamide B

Org Lett. 2020 Jun 5;22(11):4557-4561. doi: 10.1021/acs.orglett.0c01642. Epub 2020 May 28.

Abstract

The first total synthesis of the bicyclic depsipeptide natural product seongsanamide B is described. The successful approach employed solid-phase peptide synthesis of a core heptapeptide, incorporating on-resin esterification, followed by solution-phase macrolactamization and a late stage intramolecular Evans-Chan-Lam coupling to generate the biaryl ether of the isodityrosine unit.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Products / chemical synthesis*
  • Biological Products / chemistry
  • Molecular Conformation

Substances

  • Biological Products