100662-33-7

Upstream product

• 85207-15-4 allyl 2,3:4,6-di-O-isopropylidene-α-D-mannopyranoside 
• 41308-76-3 allyl α-D-mannopyranoside 
• 530-26-7 D-Mannose 
• 85207-16-5 allyl 2,3-O-isopropylidene-α-D-mannopyranoside 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 100639-33-6 propyl 4-O-(3,6-di-O-methyl-β-D-glucopyranosyl)-2,3-di-O-methyl-α-D-rhamnopyranoside 
• 100639-31-4 allyl 4-O-(2,4-di-O-benzyl-3,6-di-O-methyl-β-D-glucopyranosyl)-α-D-rhamnopyranoside 
• 100639-30-3 allyl 4-O-(2,4-di-O-benzyl-3,6-di-O-methyl-β-D-glucopyranosyl)-2,3-O-isopropylidene-α-D-rhamnopyranoside 
• 100639-27-8 allyl 4-O-benzyl-α-D-rhamnopyranoside 
• 89821-77-2 (3aS,4S,6R,7R,7aS)-4-Allyloxy-7-benzyloxy-2,2,6-trimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran 
• 100639-32-5 allyl 4-O-(2,4-di-O-benzyl-3,6-di-O-methyl-β-D-glucopyranosyl)-2,3-di-O-methyl-α-D-rhamnopyranoside 

Relevant academic research and scientific papers

SYNTHESIS OF PROPYL 4-O-(3,6-DI-O-METHYL-β-D-GLUCOPYRANOSYL)-2,3-DI-O-METHYL-α-D-RHAMNOPYRANOSIDE

Partial hydrolysis of allyl 2,3:4,6-di-O-isopropylidene-α-D-mannopyranoside gave allyl 2,3-O-isopropylidene-α-D-mannopyranoside which was converted into allyl 2,3-O-isopropylidene-α-D-rhamnopyranoside by reduction of the 6-O-tosyl derivative with lithium