107657-41-0

Upstream product

• 59995-47-0 (S)-4-hydroxycyclopent-2-en-1-one 
• 58479-61-1 tert-butylchlorodiphenylsilane 

Downstream Products

• 848750-10-7 3-tert-butoxymethyl-4-(tert-butyl-diphenyl-silanyloxy)-cyclopentanone 
• 219308-83-5 methyl 4-<3α,5α-bis-<(tert-butyldiphenylsilyl)oxy>-2β-<<(3S)-(tert-butyldiphenylsilyl)oxy>-(E,Z)-1,5-undecadien>-1β-cyclopentane>but-2-ene-1-oate 
• 219308-85-7 methyl 4-<3α,5α-bis-<(tert-butyldiphenylsilyl)oxy>-2β-<<(3S)-(tert-butyldiphenylsilyl)oxy>-(E,Z)-1,5-undecadien>-1β-cyclopentane>butanoate 
• 219309-16-7 methyl 2-<3α,5α-bis-<(tert-butyldiphenylsilyl)oxy>-2β-<<(3S)-(tert-butyldiphenylsilyl)oxy>-(E,Z)-1,5-undecadien>-1β-cyclopentane>acetate 
• 219309-18-9 2-<3α,5α-bis-<(tert-butyldiphenylsilyl)oxy>-2β-<<(3S)-(tert-butyldiphenylsilyl)oxy>-(E,Z)-1,5-undecadien>-1β-cyclopentane>ethan-1-ol 
• 219308-81-3 2-<3α,5α-bis-<(tert-butyldiphenylsilyl)oxy>-2β-<<(3S)-(tert-butyldiphenylsilyl)oxy>-(E,Z)-1,5-undecadien>-1β-cyclopentane>ethan-1-al 
• 219308-78-8 methyl 2-<3α,5α-bis-<(tert-butyldiphenylsilyl)oxy>-2β-<(3S)-(E,Z)-1,5-undecadien-3-ol>-1β-cyclopentane>acetate 
• 219308-76-6 methyl 2-<3α,5α-bis-<(tert-butyldiphenylsilyl)oxy>-2β-<(E,Z)-1,5-undecadien-3-one>-1β-cyclopentane>acetate 
• 219308-70-0 (1S,2R,3R,6S,7S,9R)-2,3-dihydroxy-7,9-bis-<(tert-butyldiphenylsilyl)oxy>bicyclo<4.3.0>non-4-one 
• 219308-65-3 (1S,6S,7S,9R)-4,4-dimethoxy-7,9-bis-<(tert-butyldiphenylsilyl)oxy>bicyclo<4.3.0>non-3-en 
• 219308-72-2 methyl 2-<3α,5α-bis-<(tert-butyldiphenylsilyl)oxy>-2β-(carboxaldehyde)-1β-cyclopentane>-acetate 
• 219308-67-5 (1S,6S,7S,9R)-7,9-bis-<(tert-butyldiphenylsilyl)oxy>bicyclo<4.3.0>non-2-en-4-one 
• 219308-63-1 (1S,6S,7S,9S)-4,4-dimethoxy-7-<(tert-butyldiphenylsilyl)oxy>bicyclo<4.3.0>non-3-en-9-ol 
• 848750-12-9 (1R,3S,4R)-3-(tert-butyldiphenylsilyloxy)-4-(tert-butoxymethyl)cyclopentanol 

Relevant academic research and scientific papers

Diels-Alder approach to isoprostanes. Total synthesis of iPF(2α)-V

Isoprostanes (iPs) are a group of natural products formed in vivo by a free-radical oxygenation of arachidonic acid. They are isomeric with prostaglandins; whereas enzymatically produced prostaglandins, such as PGF(2α) have the two side chains in the tran