Synthesis of type II beta-turn surrogate dipeptides based on syn-alpha-amino-alpha,beta-dialkyl-beta-lactams

Org Lett. 2004 Nov 25;6(24):4443-6. doi: 10.1021/ol048348c.

Abstract

The achiral bis(trimethylsilyl)methyl group acts as an efficient stereochemical determinant of the alpha-alkylation reaction in beta-branched alpha-phenyloxazolidinyl- or alpha-diphenyloxazolidinyl-beta-lactams and provides the first stereocontrolled access to syn-alpha-amino-alpha,beta-dialkyl(aryl)-beta-lactams. These products are readily transformed into type II beta-turn mimetic surrogates 2B. [reaction: see text]

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkylation
  • Dipeptides / chemical synthesis*
  • Dipeptides / chemistry
  • Protein Structure, Secondary
  • Stereoisomerism
  • beta-Lactams / chemical synthesis*
  • beta-Lactams / chemistry

Substances

  • Dipeptides
  • beta-Lactams