65657-41-2

Upstream product

• 148760-87-6 1-acetyloxy-1-(3-butenyl)cyclohexane 
• 1773-40-6 1-but-3-enyl-cyclohexanol 
• 65657-40-1 3-(1-acetyloxycyclohexyl)-1-propanol 
• 65657-39-8 1-(1-Acetyloxycyclohexyl)-3-benzyloxy-1-propyne 

Downstream Products

• 148760-95-6 ethyl (E)-5-(1-acetyloxycyclohexyl)-2-pentenoate 
• 65715-88-0 methyl 7-{2-[2-(1-acetyloxycyclohexyl)ethyl]-4-oxo-3-thiazolidinyl}heptanoate 

Relevant academic research and scientific papers

A tandem ester cleavage-Michael addition reaction for the synthesis of oxygen heterocycles

A tandem ester cleavage-Michael addition sequence has been developed for the preparation of five- and six-ring oxygen heterocycles bearing an acetic acid residue at C-2. Treatment of ethyl 6- or 7-acetyloxy-2-alkenoates with ethanolic sodium ethoxide affo

Certain thiazolidine compounds

This invention relates to novel 8-aza-9-oxo-11-thia-, -11-oxothia-, and -11-dioxothia-prostanoic acid compounds, salts, and derivatives thereof and also to processes for the preparation of such compounds. These compounds have prostaglandin-like biological activity and are particularly useful as renal vasodilators, for the treatment of certain autoimmune diseases, and in preventing thrombus formation.