64929-62-0

Upstream product

• 2944-47-0 o-isopropylanisole 
• 24591-33-1 4-bromo-2-isopropylanisole 
• 31825-29-3 3‐isopropyl‐4‐methoxybenzaldehyde 
• 88-69-7 2-(1-methylethyl)phenol 
• 134435-48-6 3-(1-methylethenyl)-4-methoxyphenylethyl acetate 
• 134435-50-0 (3-Isopropyl-4-methoxy-phenyl)-acetaldehyde 
• 39863-70-2 2-(3-isopropyl-4-methoxyphenyl)ethan-1-ol 
• 31816-29-2 4-Methoxy-3-isopropylbenzyl alcohol 

Downstream Products

• 31859-25-3 4-Methoxy-3-isopropylphenylacetonitrile 
• 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 
• 134435-52-2 7-cyano-3-phenylthio-12-methoxyabieta-8,11,13-triene 
• 514-62-5 ferruginol 
• 64158-72-1 2-Isopropyl-1-methoxy-4-[2-(2,6,6-trimethyl-cyclohex-1-enyl)-ethyl]-benzene 
• 134435-52-2 7-Cyano-3-phenylthio-12-methoxyabieta-8,11,13-triene 
• 134435-55-5 7-Keto-3-phenylsulfinyl-12-methoxyabieta-8,11,13-triene 
• 134435-53-3 7-Oxo-3-phenylthio-12-methoxyabieta-8,11,13-triene 
• 134435-54-4 7-Keto-3-phenylthio-12-methoxyabieta-2,8,11,13-tetraene 
• 61494-73-3 3,7-Diketo-12-hydroxyabieta-8,11,13-triene 

Relevant academic research and scientific papers

Syntheses and evaluation of multicaulin and miltirone-like compounds as antituberculosis agents

Four multicaulin and miltirone-like phenanthrene derivatives were synthesised and evaluated as antituberculosis agents. The crucial step of the synthesis was Pschorr coupling of 4-(3-isopropyl-4-methoxyphenyl)-2-(2-aminophenyl)ethane (13) to give 2-isopro

Approach to the synthesis of candelabrone and synthesis of 3,7-diketo-12-hydroxyabieta-8,11,13-triene

An approach to the synthesis of aromatic diterpenes was tested for its generality.Phenylacetonitriles with increasing substitution on the aromatic ring were prepared and alkylated with geranyl bromide and the resulting dienes subjected to cationic cycliza

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.