679812-46-5

Upstream product

• 679812-45-4 phenyl 2-O-acetyl-3,4-di-O-benzoyl-α-L-rhamnopyranosyl-(1->3)-2-O-acetyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside 
• 73-34-7 L-rhamnose 
• 685136-14-5 phenyl 2-O-acetyl-3,4-di-O-benzoyl-α-L-rhamnopyranosyl-(1->3)-4,6-O-benzylidene-1-thio-β-D-glucopyranoside 
• 685136-13-4 allyl 2-O-acetyl-3,4-di-O-benzoyl-α-L-rhamnopyranoside 
• 224622-44-0 allyl 2-O-acetyl-3,4-di-O-benzoyl-α-L-rhamnopyranosyl trichloroacetimidate 
• 224622-41-7 3,4-di-O-benzoyl-2-O-acetyl-α-L-rhamnopyranose 
• 201056-61-3 phenyl 2-O-acetyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside 
• 152983-23-8 phenyl 2,3-di-O-acetyl-4,6-di-O-benzylidene-1-thio-β-D-glucopyranoside 
• 98-88-4 benzoyl chloride 
• 71676-30-7 (2R,4aR,6S,7R,8R,8aS)-2-Phenyl-6-phenylsulfanyl-hexahydro-pyrano[3,2-d][1,3]dioxine-7,8-diol 

Relevant academic research and scientific papers

Synthesis of Trisaccharide of Incanoside from Caryopteris incana

Trisaccharide phenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl-(1 → 2)-3,4-di-O-benzoyl-α-L-rhamnopyranosyl-(1 → 3)-2-O-acetyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside, the sugar core of incanosides from Caryopteris incana (THUNB.), was syn

An Efficient and Regioselective Deprotection Method for Acetylated Glycosides

A new regioselective 2-O-deacetylation methodology of acetylated glycosides using 85% hydrazine hydrate in THF is described. Using this method, acetylated 1-thio-glycoside could also be selectively deprotected to give 3-O-deprotected compound.