1245189-96-1

Upstream product

• 475672-25-4 allyl L-rhamnopyranoside 
• 1609449-89-9 C₂₅H₃₀O₆ 
• 108-24-7 acetic anhydride 
• 1609449-62-8 C₂₃H₂₈O₅ 
• 1609449-60-6 C₁₆H₂₂O₅ 

Downstream Products

• 1609449-63-9 C₄₆H₄₄O₇ 
• 1053179-24-0 p-tolyl 2-O-acetyl-3,4-di-O-benzyl-1-thio-α-L-rhamnopyranoside 
• 1431974-55-8 C₄₆H₅₂O₁₁ 
• 1431974-53-6 benzyl (2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl)-(1→4)-2,3-di-O-benzyl-1-deoxy-1-(prop-2-enyl)-β-D-galactopyranuronate 
• 106848-97-9 2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl bromide 
• 1431974-58-1 C₃₂H₃₄O₇ 

Relevant academic research and scientific papers

Total synthesis of the antitumor natural product polycarcin v and evaluation of its DNA binding profile

The convergent total synthesis of polycarcin V, a gilvocarcin-type natural product that shows significant cytotoxicity with selectivity for nonsmall-cell lung cancer, breast cancer, and melanoma cells, has been achieved in 13 steps from 7, 8, and 22; the