Via Ugi reactions to conformationally fixed cyclic peptides

Chem Commun (Camb). 2003 Mar 7:(5):596-7.

Abstract

A simple approach to several cyclopeptidmimetics containing an N-alkylated amino acid was found via a multicomponent reaction followed by a ring-closing metathesis starting from readily available precursors. The combinatorial technique has the advantage that different polar, hydrophilic or hydrophobic moieties can be placed at any position in the cycles and unnatural amino acids can also be incorporated.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkylation
  • Amino Acids / chemistry
  • Crystallography, X-Ray
  • Cyclization
  • Peptides, Cyclic / chemistry*
  • Protein Conformation*
  • Structure-Activity Relationship

Substances

  • Amino Acids
  • Peptides, Cyclic