110939-39-4

Upstream product

• 768-60-5 4-methoxyphenylacetylen 
• 60512-57-4 1-(2,2-dibromovinyl)-4-methoxybenzene 
• 2408-37-9 2,2,6-trimethylcyclohexan-1-one 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 109558-42-1 2,2,6-trimethyl-1-[2-(4-methoxyphenyl)ethyl]cyclohexanol 
• 80994-24-7 1-(p-methoxyphenylethyl)-2,6,6-trimethylcyclohex-1-ene 
• 80994-30-5 1-(p-methoxyphenylethenyl)-2,6,6-trimethylcyclohex-1-ene 
• 80994-29-2 1-(p-methoxyphenylethynyl)-2,6,6-trimethylcyclohex-1-ene 
• 80994-23-6 trans-1-(p-methoxyphenylethyl)-2,2,6-trimethylcyclohexanol 

Relevant academic research and scientific papers

Synthesis of dl-standishinal and its related compounds for the studies on structure-activity relationship of inhibitory activity against aromatase

dl-Standishinal (1), an aromatase inhibitor isolated from Thuja standishii, was synthesized in 15 steps from p-formylanisole via aldol reaction of 12-hydroxy-6,7-secoabieta-8,11,13-trien-6,7-dial (2). In the present study, we found that the aldol condensa

Diterpene Synthesis. Part 2. Acid-catalysed Cyclisation of p-Methoxyphenylethyltrimethylcyclohexanols

The acid-catalysed reactions of two phenylethylcyclohexanols, precursors to tricyclic diterpenoids, are reported.The reaction produced both a bicyclic alkene and a tricyclic molecule; the former was converted into the latter in protic media.Conditions for