175662-37-0

Upstream product

• 807377-39-5 4-methyl-4-(4-methoxyphenyl)cyclopent-2-en-1-ol 
• 108454-55-3 3-(4-methoxyphenyl)-2-butenoic acid ethyl ester 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 149520-42-3 3-(4-methoxyphenyl)-but-2-en-1-ol 
• 171083-71-9 4-(4-Methoxy-phenyl)-4-methyl-hex-5-en-2-one 
• 807377-18-0 5-methyl-5-(4-methoxyphenyl)hepta-1,6-dien-3-ol 
• 174229-47-1 3-(4-methoxyphenyl)-3-methylpent-4-enal 
• 175662-33-6 2-(4-Methoxy-phenyl)-2-methyl-4-oxo-pentanal 

Downstream Products

• 807377-62-4 4-(4-methoxyphenyl)-4,5,5-trimethylcyclopent-2-enone 

Relevant academic research and scientific papers

Total synthesis of (±)-infuscol A and (±)-cuprenenol

Total synthesis of the nonaromatic cuparenoid sesquiterpenes (±)-infuscol A and cuprenenol, and (±)-infuscol B and neocuprenenol isolated from the Japanese liverwort Jungermannia infusca has been accomplished. Two ring-closing metathesis reaction based st

A simple strategy for spirocyclopentannulation of cyclic ketones. Formal total synthesis of (±)-acorone

A general and simple methodology for spirocyclopentannulation of cyclic ketones (or 4,4-disubstituted cyclopentenones from acyclic ketones) and its application in the synthesis of the spirodienone 7 via a prochiral precursor constituting a formal total synthesis of (±)-acorone (6), are described.