677766-64-2

Upstream product

• 108869-64-3 3,4,6-tri-O-benzyl-2-O-acetyl-α-D-glucosyl trichloroimidate 
• 75-08-1 ethanethiol 
• 108-24-7 acetic anhydride 

Downstream Products

• 55659-53-5 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-glucopyranosyl bromide 
• 677766-78-8 7-benzyloxy-3-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-glucopyranosyl)-2-[(4-benzyloxy-3-hydroxy)phenyl]-5-hydroxy-4H-1-benzopyran-4-one 
• 677766-61-9 5,7-bis(benzyloxy)-3-(3,4,6-tri-O-benzyl-β-D-glucopyranosyl)-2-[3,4-bis(benzyloxy)phenyl]-5-hydroxy-4H-1-benzopyran-4-one 
• 677766-79-9 5,7-bis(benzyloxy)-3-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-glucopyranosyl)-2-[3,4-bis(benzyloxy)phenyl]-5-hydroxy-4H-1-benzopyran-4-one 

Relevant academic research and scientific papers

Investigation of α-Thioglycoside Donors: Reactivity Studies toward Configuration-Controlled Orthogonal Activation in One-Pot Systems

The influence of anomeric configuration upon thioglycoside donors remains relatively unexplored. Utilizing methodology developed for the stereoselective and high-yielding synthesis of α-glycosyl thiols, a series of α-thioglycosides were synthesized, and their reactivity was compared to that of their β-counterparts. The highly selective activation observed for anomeric pairs containing a 2-O-acyl moiety and additional findings are reported. Application of a pair of superarmed thioglycosides to a one-pot oligosaccharide system is also described, in which selectivity is a result of configuration-based orthogonal activation.

Total Synthesis of Quercetin 3-Sophorotrioside

5,7-Dihydroxy-3-[β-D-glucopyranosyl-(1→2)-β -D-glucopyranosyl-(1→2)-β-D-glucopyranosyl]-2-(3,4-dihydroxyphenyl) -4H-1-benzopyran-4-one (quercetin 3-sophorotrioside), a flavonol triglycoside, isolated from Pisum sativum shoots and showing protective effect