Synthesis of stereochemically and skeletally diverse fused ring systems from functionalized C-glycosides

J Org Chem. 2013 Jun 7;78(11):5160-71. doi: 10.1021/jo4000916. Epub 2013 May 21.

Abstract

A diversity-oriented synthesis (DOS) strategy was developed for the synthesis of stereochemically diverse fused-ring systems containing a pyran moiety. Each scaffold contains an amine and methyl ester for further diversification via amine capping and amide coupling. Scaffold diversity was evaluated in comparison to previously prepared scaffolds by a shape-based principal moments of inertia (PMI) analysis.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Glycosides / chemical synthesis*
  • Glycosides / chemistry
  • Molecular Conformation
  • Pyrans / chemistry
  • Stereoisomerism

Substances

  • Glycosides
  • Pyrans