71841-61-7

Upstream product

• 35633-35-3 2-methoxy-4-methylacetophenone 
• 1257259-82-7 ethyl 5-(2-methoxy-4-methylphenyl)hex-4-enoate 
• 1257259-78-1 2-(2-methoxy-4-methylphenyl)but-3-en-2-ol 

Downstream Products

• 17194-58-0 2-(1,5-dimethyl-4-hexenyl)-5-methylphenol 
• 66879-51-4 2-methoxy-4-methyl-1-(6-methylhept-5-en-2-yl)benzene 
• 122427-58-1 4-(2'-methoxy-4'-methylphenyl)-n-pentyldimethylcarbinol 

Relevant academic research and scientific papers

Syntheses of (±)-curcuphenol, (±)-curcudiol and (±)-curcuhydroquinone: A Johnson-Claisen rearrangement approach

The synthesis of (±)-curcuphenol 1, (±)-curcudiol 2, (±)-curcuhydroquinone 3 and (±)-curcuquinone 4 had been achieved, in which the Johnson-Claisen rearrangement was used as key step.

Synthesis of bisabolane sesquiterpenes: A Johnson-Claisen rearrangement approach

Several bisabolane sesquiterpenes, (±)-curcumene, (±)-curcuphenol, (±)-curcudiol and (±)-curcuhydroquinone, have been synthesized in racemic form and fully characterized. The salient characteristic of our approach is that a Johnson-Claisen arrangement was