16790-34-4

Upstream product

• 67-56-1 methanol 
• 87733-76-4 mukurozisaponin Y₁ 

Downstream Products

• 84730-54-1 methyl per-O-acetyl-6,6'-di-O-trityl-β-sophoroside 
• 76707-65-8 methyl 3,4,6-tri-O-benzoyl-2-O-(2,3,6-tri-O-benzoyl-β-D-glucopyranosyl)-β-D-glucopyranoside 
• 76724-80-6 methyl 4,5-di-O-benzoyl-2-O-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-β-D-glucopyranoside 
• 76724-79-3 methyl 3,4,6-tri-O-benzoyl-2-O-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-β-D-glucopyranoside 
• 84730-68-7 methyl 3,2',3'-tri-O-acetyl-4,6:4',6'-di-O-benzylidene-β-sophoroside 
• 84730-69-8 methyl 3,2',3'-tri-O-acetyl-4,4'-di-O-benzoyl-6,6'-dibromo-6,6'-dideoxy-β-sophoroside 
• 84730-67-6 methyl 4,6:4',6'-di-O-benzylidene-β-sophoroside 

Relevant academic research and scientific papers

SELECTIVE CLEAVAGE OF ESTER TYPE GLYCOSIDE-LINKAGES AND ITS APPLICATION TO STRUCTURE DETERMINATION OF NATURAL OLIGOGLYCOSIDES

On treatment with anhydrous LiI, 2,6-lutidine and anhydrous methanol, an ester type glycosyl linkage of acidic tri- and di-terpenes was selectively cleaved without decomposition of a reducing terminal of the resulting sugar moiety to give an anomeric mixture of methyl glycosides along with an aglycone or a pro-aglycone in quantitative yield.In this reaction, no hydrolysis of any other glycoside linkages took place.