153094-00-9

Upstream product

• 99049-67-9 tert-Butyldimethylsilyl-2-azido-2-desoxy-β-D-glucopyranosid 
• 100-39-0 benzyl bromide 
• 138923-10-1 2-azido-4,6-O-benzylidene-2-deoxyl-1-O-tert-butyldimethylsilyl-β-D-glucopyranoside 
• 1125-88-8 benzaldehyde dimethyl acetal 

Downstream Products

• 136505-41-4 tert-butyldimethylsilyl O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1<*>3)-2-azido-6-O-benzyl-2-deoxy-β-D-glucopyranoside 
• 153094-02-1 tert-butyldimethylsilyl O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1<*>4)-2-azido-6-O-benzyl-2-deoxy-β-D-glucopyranoside 
• 144674-59-9 tert-butyldimethylsilyl O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->4)-<(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->3)>-2-azido-6-O-benzyl-2-deoxy-β-D-glucopyranoside 

Relevant academic research and scientific papers

Glycosyl Imidates, 65. Efficient Synthesis of the Lewis Antigen X (Lex) Family

tert-Butyldimethylsilyl 2-azido-4,6-O-benzylideneglucopyranoside 5 proved to be a versatile starting material for the synthesis of the Lex antigen family. 3-O-Fucosylation of 5, ensuing reductive benzylidene ring cleavage, and then 4-O-galactos

AN EFFICIENT SYNTHESIS OF THE LEWIS A (Lea) ANTIGEN PENTASACCHARIDE MOIETY

Starting material for the synthesis of Lewis A pentasaccharide (1) was azidoglucose derivative 2 which was readily transformed into the 3,4-O-unprotected derivative 3 of the 3-O-unprotected derivative 5, respectively.Reaction of 3 and O-galactosyltrichlor