954416-26-3

Upstream product

• 954416-38-7 C₃₂H₃₆O₆ 
• 954416-33-2 C₃₅H₄₀O₃Si 
• 954416-34-3 C₃₈H₄₄O₅Si 
• 954416-35-4 C₃₈H₄₆O₅Si 
• 954416-36-5 C₂₂H₂₈O₅ 
• 954416-37-6 C₂₃H₂₈O₄ 
• 954416-29-6 C₂₁H₂₄O₄ 
• 954416-27-4 C₃₄H₄₀O₆ 
• 954416-30-9 (4R)-4-((S)-1-(4-methoxybenzyloxy)allyl)-2,2-dimethyl-1,3-dioxolane 
• 954416-31-0 (2R,3S)-3-(4-methoxybenzyloxy)pent-4-ene-1,2-diol 
• 954416-28-5 C₁₃H₁₈O₃ 
• 18524-19-1 (S)-1-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-prop-2-en-1-ol 
• 118207-36-6 (2R,3S)-1,2-epoxy-3-<(4-methoxybenzyl)oxy>pent-4-ene 
• 71769-39-6 (4R,5R,4'R)-5-Iodomethyl-2,2,2',2'-tetramethyl-[4,4']bi[[1,3]dioxolanyl] 

Downstream Products

• 954416-39-8 (2R,3S,6R,7S)-6,7-di(benzyloxy)-2-methyl-10-oxo-3,6,7,8,9,10-hexahydro-2H-3-oxecinyl (E)-but-2-enoate 
• 188605-15-4 aspinolide B 

Relevant academic research and scientific papers

Stereoselective total synthesis of (-)-aspinolide B from (R)-2,3-O-isopropylideneglyceraldehyde

A stereoselective total synthesis of (-)-aspinolide B by a convergent strategy is reported. Georg Thieme Verlag Stuttgart.

Total synthesis of aspinolide B: a ring-closing metathesis approach

A highly convergent stereoselective total synthesis of aspinolide B, a 10-membered lactone is described. The key step includes a ring-closing metathesis reaction to construct the 10-membered ring and the E-olefinic moiety. d-Mannitol was used as a chiral