A new synthetic access to bicyclic polyhydroxylated alkaloid analogues from pyranosides

Org Biomol Chem. 2010 Jun 7;8(11):2639-49. doi: 10.1039/b923180c. Epub 2010 Apr 7.

Abstract

A facile, versatile and stereoselective synthesis of bicyclic polyhydroxylated alkaloids as castanospermine analogues is described. The synthetic route started from methyl pyranosides. The key steps involved a high-yielding expeditious one-pot tandem reaction from alkenes to N-substituted delta-lactams. The delta-lactams were stereoselectively vinylated to give the dienes, which were followed by the ring-closing metathesis to produce the cyclized products. The functional group transformations of the resulting bicyclic compounds furnished diverse polyhydroxylated alkaloids in good yields.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaloids / chemical synthesis
  • Alkaloids / chemistry*
  • Bridged Bicyclo Compounds / chemistry*
  • Glycosides / chemistry*
  • Hydroxylation
  • Polymers / chemical synthesis*
  • Polymers / chemistry
  • Pyrans / chemistry*
  • Stereoisomerism

Substances

  • Alkaloids
  • Bridged Bicyclo Compounds
  • Glycosides
  • Polymers
  • Pyrans