Total synthesis of a 20-deoxybryostatin

Chem Commun (Camb). 2011 Jul 7;47(25):7200-2. doi: 10.1039/c1cc12332g. Epub 2011 May 26.

Abstract

The 20-deoxybryostatin 40 has been prepared using a modified Julia olefination to form the 16,17-double-bond, followed by macrolactonisation, selective deprotection and oxidation. This is the first total synthesis of a 20-deoxybryostatin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bryostatins / chemical synthesis*
  • Bryostatins / chemistry
  • Ethers
  • Oxidation-Reduction
  • Substrate Specificity

Substances

  • 20-deoxybryostatin
  • Bryostatins
  • Ethers