77875-54-8

Upstream product

• 18039-26-4 2,3,4-tri-O-benzyl-D-xylopyranose 
• 20787-16-0 2,3,4-tri-O-benzyl-α-D-xylopyranose 
• 121916-92-5 2,3,4-tri-O-benzyl-α-D-xylopyranosyl chloride 

Downstream Products

• 77875-55-9 (2,3,4-tri-O-benzyl-β-L-arabinopyranosyl)-2,3,4-tri-O-benzyl-β-L-arabinopyranoside 

Relevant academic research and scientific papers

Synthesis and glycosylation shift of 1,1'-disaccharides

Nineteen kinds of nonreducing 1,1'-disaccharides have synthesized by modified Koenigs-Knorr method, and characterized by NMR. The glycosylation shift of each anomeric carbon has been estimated.

Molecular sieves promote stereocontrolled αα-disaccharide formation via direct dimerization of free sugars

Some commercial molecular sieves promote direct dimerization of free pyranose and furanose sugars stereoselectively into the corresponding α,α-disaccharides.

TMS triflate induced synthesis of 1,1'-disaccharides from 1-hydroxy sugars

A variety of 1,1'-disaccharides have been prepared by TMS triflate induced coupling of 1-hydroxy sugars in reasonable yield.

Mecanisme de la reaction de glycosylation par reversion acide en presence d'anhydride trifluoromethane sulfonique comme agent de condensation

The acid-catalysed mechanism of the reaction using trifluoromethanesulfonic anhydride to synthesize symmetrical 1,1'-glycosyl-clycosides such as trehalose and galacto, manno, arabino, xylo etc. analogues has been elucidated.The authors were able to prove