251292-82-7

Upstream product

• 1745-17-1 methyl hept-6-enoate 
• 251292-80-5 7-{(1R,2R,3R,5S)-5-Acetoxy-3-(tert-butyl-dimethyl-silanyloxy)-2-[(E)-(S)-3-(tert-butyl-diphenyl-silanyloxy)-oct-1-enyl]-cyclopentyl}-heptanoic acid methyl ester 
• 251292-77-0 7-{(1R,2R,3R,5S)-3-(tert-Butyl-dimethyl-silanyloxy)-2-[(E)-(S)-3-(tert-butyl-diphenyl-silanyloxy)-oct-1-enyl]-5-hydroxy-cyclopentyl}-heptanoic acid methyl ester 
• 150686-70-7 (R)-4-((tert-butyldimethylsilyl)oxy)-2-iodocyclopent-2-en-1-one 
• 61305-35-9 (R)-4-((tert-butyldimethylsilyl)oxy)cyclopent-2-enone 
• 41138-69-6 7-{3-[(tert-butyldimethylsilanyl)oxy]-5-oxocyclopent-1-en-1-yl}heptanoic acid methyl ester 
• 251292-81-6 7-{(1R,2R,3R,5S)-5-Acetoxy-2-[(E)-(S)-3-(tert-butyl-diphenyl-silanyloxy)-oct-1-enyl]-3-hydroxy-cyclopentyl}-heptanoic acid methyl ester 

Downstream Products

• 251292-83-8 7-{(1S,5R)-5-[(E)-(S)-3-(tert-Butyl-diphenyl-silanyloxy)-oct-1-enyl]-4-oxo-cyclopent-2-enyl}-heptanoic acid methyl ester 

Relevant academic research and scientific papers

Synthesis and antiviral activity of prostaglandin-J1 methyl ester

A prostagIandin-F, a methyl ester derivative (12) possessing three different protecting groups on the hydroxy units was prepared so as to allow selective removal of the group attached to the 11-OH group. Compound (12) was converted into prostaglandin-J, m