Mimics of L-rhamnose: Analogues of rhamnopyranose containing a constituent alpha-amino acid at the anomeric position. A rhamnopyranose analogue of hydantocidin

  • Estevez, JC
  • Smith, MD
  • Wormald, MR
  • Besra, GS
  • Brennan, PJ
  • Nash, RJ
  • Fleet, GWJ
Publication date
February 1996
Publisher
Elsevier BV
Journal
Tetrahedron Asymmetry

Abstract

Ionic brominative oxidation of 2-amino derivatives of protected heptonolactones derived from L-rhamnose provides a key bicyclic intermediate for the synthesis of analogues of L-rhamnopyranose with spirohydantoins and spirodiketopiperazines at the anomeric position; the same intermediate can be used for the synthesis of novel glycopeptides containing a constituent rhamnopyranose amino acid. such materials may allow an approach to new studies of diseases induced by mycobacteria, such as tuberculosis and leprosy

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