333968-48-2

Upstream product

• 108-24-7 acetic anhydride 
• 333968-44-8 benzyl {4-[3,5-bis(tert-butyldimethylsilyloxy)-2-[3-(tert-butyldimethylsilyloxy)-4-phenoxybutyl]-cyclopentyl]butylamino}acetate 
• 150686-70-7 (R)-4-((tert-butyldimethylsilyl)oxy)-2-iodocyclopent-2-en-1-one 
• 108-95-2 phenol 
• 333968-36-8 2-[4-(benzyloxy)butyl]-1,4-bis(tert-butyldimethylsilyloxy)-3-[3-(tert-butyldimethylsilyloxy)-4-phenoxybutyl]-cyclopentane 
• 333968-41-5 4-{3,5-bis(tert-butyldimethylsilyloxy)-2-[3-(tert-butyldimethylsilyloxy)-4-phenoxybutyl]cyclopentyl}-1-butanol 
• 333968-40-4 2-[4-(benzyloxy)butyl]-4-(tert-butyldimethylsilyloxy)-3-[3-(tert-butyldimethylsilyloxy)-4-phenoxybutyl]-cyclopentan-1-one 
• 333968-43-7 4-{3,5-bis(tert-butyldimethylsilyloxy)-2-[3-(tert-butyldimethylsilyloxy)-4-phenoxybutyl]cyclopentyl}butanal 
• 333968-39-1 (4R)-2-[4-(benzyloxy)butyl]-4-(tert-butyldimethylsilyloxy)-2-cyclopenten-1-one 
• 333968-37-9 (R)-2-(tert-butyldimethylsilyloxy)-4-iodo-1-phenoxybutane 
• 333968-38-0 (R)-4-Bromo-1-phenoxy-butan-2-ol 

Relevant academic research and scientific papers

An efficient synthesis of 3-hetero-13,14-dihydro prostaglandin F1α analogues

Matrix presented A new class of 3-hetero-13,14-dihydro prostaglandin F1α analogues was synthesized from a common intermediate. The latter was constructed via a two-step, three-component process. The lower chain, containing the 15-(phenoxymethyl