Total synthesis of mycocyclosin

Org Lett. 2012 May 4;14(9):2402-5. doi: 10.1021/ol300831t. Epub 2012 Apr 20.

Abstract

The first total synthesis of mycocyclosin, a diketopiperazine natural product isolated from M. tuberculosis, is described. While direct oxidative coupling of tyrosine phenolic groups was unsuccessful, construction of the highly strained bicyclic framework was successfully accomplished through an intramolecular Miyaura-Suzuki cross-coupling to generate the biaryl linkage.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Products / chemical synthesis*
  • Biological Products / chemistry
  • Diketopiperazines / chemical synthesis*
  • Diketopiperazines / chemistry
  • Molecular Structure
  • Mycobacterium tuberculosis / chemistry*

Substances

  • Biological Products
  • Diketopiperazines
  • mycocyclosin