259733-32-9

Upstream product

• 65253-04-5 (-)-8-phenylmenthol 
• 259733-12-5 ethyl (E)-2-methyl-2-tridecen-7-ynoate 
• 85944-93-0 undec-5-yn-1-al 
• 69222-09-9 undec-5-yn-1-ol 

Downstream Products

• 259733-33-0 (1R,2S,5R)-2-(1-methyl-1-phenylethyl)-5-methylcyclohexyl (E)-3-methyl-2-nonen-7-ynoate 
• 259733-37-4 (1R,2S,5R)-2-(1-methyl-1-phenylethyl)-5-methylcyclohexyl [(RS)-2-(1-(E)-hexylidene)cyclopent-1-yl]acetate 

Relevant academic research and scientific papers

Asymmetric synthesis of bicyclic ketones having an angular substituent via Ti(II) alkoxide-mediated tandem cyclization of trisubstituted olefinic substrates

(Formula Presentation) Angularly substituted, optically active bicyclic ketones of up to 94% ee were prepared by the Ti(II) alkoxide-mediated tandem cyclization of open-chain substrates, that is, 8-phenylmenthyl enynoates having a trisubstituted double bond.