Total synthesis of aeruginosin 98B

J Am Chem Soc. 2012 Nov 21;134(46):18944-7. doi: 10.1021/ja309947n. Epub 2012 Nov 12.

Abstract

The first total synthesis of aeruginosin 98B was accomplished. The key step is a highly diastereoselective Pd-catalyzed intramolecular asymmetric allylic alkylation reaction of a diastereomeric mixture of allylic carbonates that is enabled by the use of racemic phosphine ligand L1.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkylation
  • Catalysis
  • Oligopeptides / chemical synthesis*
  • Palladium / chemistry

Substances

  • Oligopeptides
  • aeruginosin 98-B
  • Palladium