134435-47-5

Upstream product

• 702-23-8 2-(4-Methoxyphenyl)ethanol 
• 917-64-6 methyl magnesium iodide 
• 134435-46-4 3-acetyl-4-methoxyphenylethyl acetate 

Downstream Products

• 39863-70-2 2-(3-isopropyl-4-methoxyphenyl)ethan-1-ol 
• 187161-50-8 1-isopropyl-4-methoxyphenylethyl iodide 
• 134435-49-7 1-isopropyl-4-methoxyphenylethyl acetate 
• 187161-51-9 3-Isopropoxy-6-[2-(3-isopropyl-4-methoxy-phenyl)-ethyl]-5,5-dimethyl-cyclohex-2-enone 
• 61494-73-3 12-hydroxy-abieta-8,11,13-trien-3,7-dione 
• 31816-29-2 4-Methoxy-3-isopropylbenzyl alcohol 
• 24591-33-1 4-bromo-2-isopropylanisole 
• 2944-47-0 o-isopropylanisole 
• 134435-48-6 3-(1-methylethenyl)-4-methoxyphenylethyl acetate 

Relevant academic research and scientific papers

Synthesis of 12-O-methyl-2a-methoxyferruginol

A rapid synthesis of 12-O-methyl-2-methoxyferruginol (1) shows it not to be identical with the natural product ascribed this structure.

Synthesis of aromatic diterpenes synthesis of 12-hydroxy-abieta-8,11,13-trien-3,7-dione

Model studies involving cationic cyclisation of suitable dienes have provided a synthesis of the title compound. Preparation of the dienes from available aromatic starting materials and the modification of the cyclised products are described.