71071-83-5

Upstream product

• 98-88-4 benzoyl chloride 
• 14687-15-1 methyl L-fucopyranoside 
• 73-34-7 6-deoxy-L-galactose 
• 1128-40-1 methyl β-L-fucopyranoside 
• 59981-27-0 methyl 2-O-methyl-α-D-fucopyranoside 
• 74135-23-2 methyl 3,4-O-isopropylidene-2-O-methyl-α-D-fucopyranoside 
• 4137-35-3 methyl 2,3-bis-O-benzoyl-α-D-galactopyranoside 

Downstream Products

• 117124-67-1 C₅₅H₅₆O₁₂ 
• 132867-66-4 methyl 2,3-di-O-benzoyl-6-deoxy-4-O-trifluormethanesulfonyl-α-L-galactopyranoside 
• 132867-67-5 methyl 2,3-di-O-benzoyl-4,6-dideoxy-4-iodo-α-L-glucopyranoside 
• 152646-58-7 methyl 2,3-di-O-benzoyl-4-oxo-β-L-fucopyranoside 
• 132867-68-6 methyl 2,3-di-O-benzoyl-6-deoxy-4-<(methylthio)thiocarbonyl>-α-L-galactopyranoside 
• 172949-31-4 Methyl O-<2,3-di-O-benzoyl-6-O-(4-methoxybenzyl)-β-D-glucopyranosyl>-(1->4)-2,3-di-O-benzoyl-α-L-fucopyranoside 
• 152646-59-8 methyl 2,3-di-O-benzoyl-4-(prop-2'-en-1'-yl)-6-deoxy-β-L-glucopyranoside 
• 163106-69-2 methyl 2,3-di-O-benzoyl-4-(3'-bromo-2'-oxo-prop-1'-yl)-6-deoxy-β-L-glucopyranoside 
• 152646-57-6 methyl 2,3-di-O-benzoyl-4-(3'-dimethylphosphono-2'-oxo-propan-1-yl)-6-deoxy-β-L-galactopyranoside 
• 152646-63-4 methyl 2,3-di-O-benzoyl-4-(3'-diisopropoxyphosphono-2'-oxo-prop-1'-yl)-6-deoxy-β-L-glucopyranoside 
• 152957-11-4 methyl 5-acetamido-2-<5''-(methyl 2',3'-di-O-benzoyl-6'-deoxy-β-L-galactopyranoside-4'-yl)-4''-oxo-pent-1''-yl>-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulosonate 

Relevant academic research and scientific papers

Synthesis and Structural Characteristics of all Mono- And Difluorinated 4,6-Dideoxy- d - Xylo-hexopyranoses

Protein-carbohydrate interactions are implicated in many biochemical/biological processes that are fundamental to life and to human health. Fluorinated carbohydrate analogues play an important role in the study of these interactions and find application a

Catalytic Activation of Cis-Vicinal Diols by Boronic Acids: Site-Selective Acylation of Carbohydrates

Site-selective acylation of unprotected carbohydrates by using stable, storable, and easily handled imidazole-containing organoboronic acid catalysts is described. This catalytic process with low catalyst loading enables the introduction of a wide variety of acyl functional groups into the equatorial position of cis-vicinal diols in unprotected hexapyranosides with excellent site selectivity. This is the first example that uses a Lewis base-containing boronic acid to enhance the nucleophilicity of hydroxy groups.

SYNTHESIS OF TETRASACCHARIDE REPEATING UNIT OF THE K-ANTIGEN FROM KLEBSIELLA TYPE-16

Starting from L-fucose, D-glucose and lactose, methyl O--(1->4)-2,3-di-O-benzoyl-α-L-fucopyranoside and methyl O-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)-(1->4)-O-(2,3,6-tri-O-benzyl-α

Stereochemical studies on Esperamicins: Determination of the absolute configuration of hydroxyamino sugar fragment

The β-D-gluco-hexopyranose configuration has been assigned for the hydroxyamino sugar fragment or esperamicin A. This determination concluded our study on the absolute configuration of the carbohydrate portion of esperamicins.

Synthesis of 4-deoxy and 4-deoxy-4-halogeno derivatives of L-fucose as potential enzyme inhibitors

Methyl-2,3-di-O-benzoyl-6-deoxy-α-L-galactopyranoside (2) was converted into the 4-deoxy-4-iodo-α-L-gluco derivative 4 by triflate-mediated inversion.Catalytic reduction of 4 gave methyl 2,3-di-O-benzoyl-4,6-dideoxy-α-L-xylo-hexopyranoside (6) and subsequ