134435-48-6

Upstream product

• 134435-46-4 3-acetyl-4-methoxyphenylethyl acetate 
• 134435-47-5 3-(1-hydroxy-1-methylethyl)-4-methoxyphenylethanol 
• 64-19-7 acetic acid 
• 702-23-8 2-(4-Methoxyphenyl)ethanol 

Downstream Products

• 187161-50-8 1-isopropyl-4-methoxyphenylethyl iodide 
• 187161-51-9 3-Isopropoxy-6-[2-(3-isopropyl-4-methoxy-phenyl)-ethyl]-5,5-dimethyl-cyclohex-2-enone 
• 2944-47-0 o-isopropylanisole 
• 24591-33-1 4-bromo-2-isopropylanisole 
• 31816-29-2 4-Methoxy-3-isopropylbenzyl alcohol 
• 31825-29-3 3‐isopropyl‐4‐methoxybenzaldehyde 
• 31859-25-3 4-Methoxy-3-isopropylphenylacetonitrile 
• 64929-62-0 3-isopropyl-4-methoxybenzyl bromide 
• 134435-50-0 (3-Isopropyl-4-methoxy-phenyl)-acetaldehyde 
• 134435-51-1 (E)-2-(3-Isopropyl-4-methoxy-phenyl)-5,9-dimethyl-deca-4,8-dienenitrile 
• 61494-73-3 12-hydroxy-abieta-8,11,13-trien-3,7-dione 
• 134435-54-4 7-Isopropyl-6-methoxy-1,1,4a-trimethyl-2-phenylsulfanyl-4,4a,10,10a-tetrahydro-1H-phenanthren-9-one 
• 134435-53-3 7-Isopropyl-6-methoxy-1,1,4a-trimethyl-2-phenylsulfanyl-2,3,4,4a,10,10a-hexahydro-1H-phenanthren-9-one 
• 134435-55-5 2-Benzenesulfinyl-7-isopropyl-6-methoxy-1,1,4a-trimethyl-2,3,4,4a,10,10a-hexahydro-1H-phenanthren-9-one 

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.