384371-52-2

Upstream product

• 98-88-4 benzoyl chloride 
• 384371-51-1 C₃₅H₃₆O₁₂ 
• 384371-50-0 Allyl 2',3',5'-tri-O-benzoyl-α-L-arabinofuranosyl-(1->4)-2,3-O-isopropylidene-α-L-rhamnopyranoside 
• 251451-05-5 2,3,5-tri-O-benzoyl-α-L-arabinofuranosyl 2,2,2-trichloroacetimidate 
• 100639-25-6 allyl 2,3-O-isopropylidene-α-L-rhamnopyranoside 

Downstream Products

• 384371-55-5 2^D,3^D,5^D-Tri-O-benzoyl-α-L-arabinofuranosyl-(1->4)-[2^C,3^C,4^C,6^C-tetra-O-acetyl-β-D-glucopyranosyl-(1->3)]-2^B-O-benzoyl-α-L-rhamnopyranosyl 2,2,2-trichloroacetimidate 
• 516516-81-7 C₅₃H₅₄O₂₂ 
• 384371-53-3 Allyl 2^D,3^D,5^D-tri-O-benzoyl-α-L-arabinofuranosyl-(1->4)-[2^C,3^C,4^C,6^C-tetra-O-acetyl-β-D-glucopyranosyl-(1->3)]-2^B-O-benzoyl-α-L-rhamnopyranoside 

Relevant academic research and scientific papers

An effcient synthesis of julibrosides related to neosaponin

A practical method is developed for the synthesis of neosaponin cholest-5(6)-en-3β-yl β-D-glucopyranosyl-(1→3)-[α-L-arabinofuranosyl-(1→4)]- α-L-rhamnopyranosyl-(1→2)-β-D-glucopyranoside. This julibroside mimic shows cytotoxic activity towards P388 (mouse leukaemia) with GI50 = 22.5 μg mL-1.