142041-45-0

Upstream product

• 142041-40-5 (3-endo,6-endo)-6-<<(1,1-dimethylethyl)dimethylsilyl>oxy>-3-methyl-2-oxo-7-oxabicyclo<2.2.1>heptane-2-carboxaldehyde 
• 142041-44-9 <(p-Methoxyphenoxy)methyl>triphenylphosphonium chloride 

Downstream Products

• 142041-47-2 (1E,2-endo,3-exo,6-endo)-2-(4,5-dihydro-2-furanyl)-1-<2-(4-methoxyphenoxy)ethenyl>-3-methyl-3-(phenylthio)-7-oxabicyclo<2.2.1>heptane-2,6-diol 
• 142041-48-3 (1E,2-endo,3-exo,6-endo)-6-<<(1,1-dimethylethyl)diphenylsilyl>oxy>-2-(4,5-dihydro-2-furanyl)-1-<2-(4-methoxyphenoxy)ethenyl>-3-methyl-3-(phenylthio)-7-oxabicyclo<2.2.1>heptan-2-ol 
• 142041-49-4 (3α,4β,7β,9α,10α,11aα)-7-<<(1,1-dimethylethyl)diphenylsilyl>oxy>-2,3,3a,4,7,8,9,10,11,11a-decahydro-4-(4-methoxyphenoxy)-10-methyl-10-(phenylthio)-6,9-epoxycyclodecafuran-11-one 
• 142041-49-4 (3aα,4β,7β,9α,10α,11aβ)-7-<<(1,1-dimethylethyl)diphenylsilyl>oxy>-2,3,3a,4,7,8,9,10,11,11a-decahydro-4-(4-methoxyphenoxy)-10-methyl-10-(phenylthio)-6,9-epoxycyclodecafuran-11-one 
• 142041-46-1 (1E,3-exo,6-endo)-6-<<(1,1-dimethylethyl)dimethylsilyl>oxy>-1-<2-(4-methoxyphenoxy)ethenyl>-3-methyl-3-(phenylthio)-7-oxabicyclo<2.2.1>heptan-2-one 
• 142041-47-2 (1Z,2-endo,3-exo,6-endo)-2-(4,5-dihydro-2-furanyl)-1-<2-(4-methoxyphenoxy)ethenyl>-3-methyl-3-(phenylthio)-7-oxabicyclo<2.2.1>heptane-2,6-diol 
• 142041-48-3 (1Z,2-endo,3-exo,6-endo)-6-<<(1,1-dimethylethyl)diphenylsilyl>oxy>-2-(4,5-dihydro-2-furanyl)-1-<2-(4-methoxyphenoxy)ethenyl>-3-methyl-3-(phenylthio)-7-oxabicyclo<2.2.1>heptan-2-ol 
• 142041-49-4 (3aα,4α,7β,9α,10α,11aβ)-7-<<(1,1-dimethylethyl)diphenylsilyl>oxy>-2,3,3a,4,7,8,9,10,11,11a-decahydro-4-(4-methoxyphenoxy)-10-methyl-10-(phenylthio)-6,9-epoxycyclodecafuran-11-one 
• 142041-46-1 (1Z,3-exo,6-endo)-6-<<(1,1-dimethylethyl)dimethylsilyl>oxy>-1-<2-(4-methoxyphenoxy)ethenyl>-3-methyl-3-(phenylthio)-7-oxabicyclo<2.2.1>heptan-2-one 

Relevant academic research and scientific papers

Synthetic Studies on Furanoheliangolides. Stereocontrolled Construction of the Oxygen-Bridged Tricyclic Framework

The heavily functionalized 6,9-epoxycyclodecafuran-11-ones 34 and 37 have been prepared in 13 steps from 4-methyl-2-furan.The key elements of the scheme include a high-pressure Diels-Alder cycloaddition to 1-cyanovinyl acetate, h