Stereoselective synthesis and rearrangement-fragmentation of arylidene N-alkoxydiketopiperazines

Org Biomol Chem. 2011 Nov 7;9(21):7476-81. doi: 10.1039/c1ob05722g. Epub 2011 Sep 15.

Abstract

A stereoselective synthesis of arylidene N-alkoxydiketopiperazines via oxime-ether formation and intramolecular acylation is described, followed by an acid-catalysed rearrangement-fragmentation to give novel diketopiperazine hemiaminal derivatives with useful bioactivity against certain tumour cell lines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Crystallography, X-Ray
  • Diketopiperazines / chemical synthesis*
  • Diketopiperazines / chemistry*
  • Models, Molecular
  • Molecular Conformation
  • Stereoisomerism

Substances

  • Diketopiperazines