Skeletal diversity from carbohydrates: use of mannose for the diversity-oriented synthesis of polyhydroxylated compounds

J Org Chem. 2015 Feb 20;80(4):2182-91. doi: 10.1021/jo502701c. Epub 2015 Feb 11.

Abstract

The application of d-mannose as a multipurpose building block from the chiral pool enabled the diversity-oriented synthesis of an array of cyclic and bicyclic scaffolds with polyhydroxylated appendages with the aim to expand the skeletal diversity in the panorama of glycopeptidomimetic compounds.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Hydroxylation
  • Mannose / chemistry*
  • Molecular Conformation
  • Peptidomimetics / chemical synthesis*
  • Peptidomimetics / chemistry

Substances

  • Peptidomimetics
  • Mannose