Cookies on this website
We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we'll assume that you are happy to receive all cookies and you won't see this message again. Click 'Find out more' for information on how to change your cookie settings.

The discovery of novel conditions for highly beta-stereoselective (>9 : 1) mannosylation of OH-2 of mannosides using a straightforward perbenzylthioglycoside donor has allowed ready assembly of beta-mannosyl oligosaccharides including the repeating trisaccharide motif of the O5 antigen of pathogen Klebsiella pneumoniae.

Original publication

DOI

10.1039/b803999m

Type

Journal article

Journal

Org Biomol Chem

Publication Date

07/08/2008

Volume

6

Pages

2692 - 2696

Keywords

Carbohydrate Conformation, Hydroxides, Mannosides, Molecular Structure, Oligosaccharides, Stereoisomerism, Thioglycosides