A synthesis of all stereoisomers of tenuecyclamide A employing a fluorous-Fmoc strategy

J Org Chem. 2013 Oct 18;78(20):10264-72. doi: 10.1021/jo401647k. Epub 2013 Oct 9.

Abstract

A concise liquid-phase combinatorial synthesis of all stereoisomers of Tenuecyclamide A was achieved using a mixture of D-/L-alanine with each stereoisomer encoded by a different f-Fmoc tag. The synthetic strategy using f-Fmoc reagents as the protecting group for amino acids has been demonstrated to be a useful method for diverse polypeptide analogue synthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine / chemistry*
  • Peptides / chemical synthesis*
  • Peptides / chemistry
  • Peptides, Cyclic / chemical synthesis*
  • Peptides, Cyclic / chemistry
  • Stereoisomerism
  • Thiazoles / chemical synthesis*
  • Thiazoles / chemistry

Substances

  • Peptides
  • Peptides, Cyclic
  • Thiazoles
  • tenuecyclamide A
  • Alanine