Stereocontrolled access to carba-C-disaccharides via functionalized dienylsilanes

  • Angelaud R
  • Landais Y
  • Parra-Rapado L
  • 3


    Mendeley users who have this article in their library.
  • 42


    Citations of this article.


We report here the total synthesis of a class of C1 → C6 Carba-C-disaccharide, formed by the association between a 2-deoxyglucose as the sugar unit and a pseudo-pyranose or a pseudo-furanose as the carba-sugar moiety. The carba-sugar fragments were assembled from the corresponding dienylsilanes through a dihydroxylation-cyclopropanation sequence.

Get free article suggestions today

Mendeley saves you time finding and organizing research

Sign up here
Already have an account ?Sign in

Find this document


  • Rémy Angelaud

  • Yannick Landais

  • Liliana Parra-Rapado

Cite this document

Choose a citation style from the tabs below

Save time finding and organizing research with Mendeley

Sign up for free