Stereocontrolled access to carba-C-disaccharides via functionalized dienylsilanes

42Citations
Citations of this article
4Readers
Mendeley users who have this article in their library.
Get full text

Abstract

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.

Cite

CITATION STYLE

APA

Angelaud, R., Landais, Y., & Parra-Rapado, L. (1997). Stereocontrolled access to carba-C-disaccharides via functionalized dienylsilanes. Tetrahedron Letters, 38(51), 8845–8848. https://doi.org/10.1016/S0040-4039(97)10389-6

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free