39863-58-6

Upstream product

• 88-69-7 2-(1-methylethyl)phenol 
• 24591-33-1 4-bromo-2-isopropylanisole 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 39863-70-2 2-(3-isopropyl-4-methoxyphenyl)ethan-1-ol 

Downstream Products

• 130487-69-3 ethyl 3-(3-isopropyl-4-methoxyphenethyl)-2-methyl-4-oxocyclohex-2-ene-1-carboxylate 
• 100172-08-5 8-(4-Methoxy-3-isopropyl-phenyl)-5-oxo-octansaeure-methylester 
• 130487-63-7 trans-<2-(3-isopropyl-4-methoxyphenethyl)-3,3-dimethylcyclohexyl>methanol 
• 130487-63-7 cis-<2-(3-isopropyl-4-methoxyphenethyl)-3,3-dimethylcyclohexyl>methanol 
• 130487-60-4 2-(3-isopropyl-4-methoxyphenethyl)-3-methylcyclohex-2-en-1-one 
• 139126-46-8 2-(3-isopropyl-4-methoxyphenethyl)-3,3-dimethylcyclohexanone 
• 130487-62-6 2-(3-isopropyl-4-methoxyphenethyl)-3,3-dimethyl-1-methylenecyclohexane 
• 128291-67-8 3-(3-isopropyl-4-methoxyphenyl)propionitrile 

Relevant academic research and scientific papers

Total synthesis of (±)-Scrodentoid A

An efficient total synthesis of scrodentoid A was accomplished starting from a Hagemann's ester and a substituted (2-bromoethyl)benzene. Key reactions in this synthesis include C-alkylation of the Hagemann's ester, 6-endo-Trig cationic cyclization of an enone and Lewis acid promoted isomerization of a cis-fused ketone.