On the Reactivity and Selectivity of Galacturonic Acid Lactones

Exploring and Exploiting the Reactivity of Glucuronic Acid Donors

(2011) Ana-Rae de Jong et al.   JOURNAL OF ORGANIC CHEMISTRY

Galacturonic Acid Lactones in the Synthesis of All Trisaccharide Repeating Units of the Zwitterionic Polysaccharide Sp1

(2011) Alphert E. Christina et al.   JOURNAL OF ORGANIC CHEMISTRY

Mannopyranosyl Uronic Acid Donor Reactivity

(2011) Marthe T. C. Walvoort et al.   ORGANIC LETTERS

A potential glucuronate glycosyl donor with 2-O-acyl-6,3-lactone structure: efficient synthesis of glycosaminoglycan disaccharides

(2011) Takayuki Furukawa et al.   TETRAHEDRON LETTERS

Synthesis of Monomeric and Dimeric Repeating Units of the Zwitterionic Type 1 Capsular Polysaccharide fromStreptococcus pneumoniae

(2010) Xiangyang Wu et al.   CHEMISTRY-A EUROPEAN JOURNAL

Glycosyl donors in “unusual” conformations – influence on reactivity and selectivity

(2010) Christian M. Pedersen et al.   COMPTES RENDUS CHIMIE

A stable, commercially available sulfenyl chloride for the activation of thioglycosides in conjunction with silver trifluoromethanesulfonate

(2008) David Crich et al.   CARBOHYDRATE RESEARCH

Conformationally armed glycosyl donors: reactivity quantification, new donors and one pot reactions

(2008) Christian Marcus Pedersen et al.   CHEMICAL COMMUNICATIONS