358740-38-2

Upstream product

• 358740-34-8 (S)-3-[(7Z,13E,17E)-(2R,10S)-2-(tert-Butyl-diphenyl-silanyloxy)-10-methoxymethoxy-triaconta-7,13,17-trienyl]-5-methyl-5H-furan-2-one 
• 358740-31-5 (3S,6E,10E)-1-tert-butyldiphenylsilyloxy-3-(methoxy)methoxy-tricosa-6,10-dien 
• 358740-32-6 (3S,6E,10E)-1-iodo-3-(methoxy)methoxy-tricosa-6,10-dien 
• 358740-42-8 (3S,6E,10E)-3-(methoxy)methoxy-tricosa-6,10-dien-1-ol 
• 358740-30-4 (3S,6E,10E)-tricosa-6,10-dien-1,3-diol 
• 358740-29-1 (2S,3S,6E,10E)-2,3-epoxytricosa-6,10-dien-1-ol 
• 358740-36-0 (S)-3-[(7Z,13E,17E)-(2R,10S)-2-(tert-Butyl-diphenyl-silanyloxy)-10-hydroxy-triaconta-7,13,17-trienyl]-5-methyl-5H-furan-2-one 

Downstream Products

• 358740-40-6 (S)-3-{(R)-2-(tert-Butyl-diphenyl-silanyloxy)-9-[(2S,5R,2'S,5'R)-5'-((R)-1-hydroxy-tridecyl)-octahydro-[2,2']bifuranyl-5-yl]-nonyl}-5-methyl-5H-furan-2-one 

Relevant academic research and scientific papers

Oxidative polycyclization with rhenium(VII) oxides: Application of the stereoselectivity rules in the total synthesis of rollidecins C and D

Rollidecin C, 1, and rollidecin D, 2, two adjacent bis-THF Annonaceous acetogenins, were synthesized from the partially functionalized 'naked' carbon skeletons 14 and 15, respectively. The retrosynthetic route to the target compounds was guided by the rec