174172-99-7

Upstream product

• 100-39-0 benzyl bromide 
• 20701-61-5 ethyl 4,6-O-benzylidene-1-thio-β-D-glucopyranoside 

Downstream Products

• 241471-10-3 ethyl 2-O-benzyl-4,6-O-benzylidene-6-O-(3-bromomethylbenzyl)-1-thio-β-D-glucopyranoside 
• 522632-95-7 ethyl 2-O-benzyl-4,6-O-benzylidene-3-O-(3-bromobenzyl)-1-thio-β-D-glucopyranoside 
• 1233488-82-8 methyl 2-O-benzyl-3, 4, 6-tri-O-benzoyl-D-glucopyranosyl-α-(1→6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside 
• 1309360-93-7 CF₃O₃S^(1-)*C₃₇H₃₇O₈S⁽¹⁺⁾ 
• 1309360-98-2 C₃₇H₃₇O₈S⁽¹⁺⁾*ClO₄^(1-) 
• 1309361-02-1 CF₃O₃S^(1-)*C₃₇H₃₇O₈S₂⁽¹⁺⁾ 
• 1309360-94-8 C₃₅H₂₉⁽²⁾H₃O₉ 
• 1309360-95-9 C₃₅H₃₂O₉ 

Relevant academic research and scientific papers

Direct synthesis of diastereomerically pure glycosyl sulfonium salts

It is reported that stable glycosyl sulfonium salts can be generated via direct anomeric S-methylation of ethylthioglycosides. Mechanistically, this pathway represents the first step in the activation of thioglycosides for glycosidation; however, it can f

Influence of the O3 protecting group on stereoselectivity in the preparation of C-mannopyranosides with 4,6-O-benzylidene protected donors

α-C-Glucopyranosides and mannopyranosides are obtained in 65-85% yields from 4,6-O-benzylidene-protected glucosyl and mannosyl thioglycosides bearing ester functionality at the 3-O-position by a coupling reaction with C-nucleophiles on activation with dip

PARTIAL SUBSTITUTION OF THIOGLYCOSIDES BY PHASE TRANSFER CATALYZED BENZOYLATION AND BENZYLATION

Partial substitution by phase transfer catalysis giving monobenzoylated and monobenzylated products from 2,3- and from 4,6-diols in ethyl 1-thio-D-hexopyranosides with the β-gluco, β-galacto- and α-manno-configurations are described.Two disaccharide thiog