678149-56-9

Upstream product

• 323195-85-3 Ethyl (2E)-3-(2,5-dimethoxy-4-methylphenyl)but-2-enoate 
• 678149-54-7 3-(2,5-dimethoxy-4-methylphenyl)but-2-enol 
• 13720-58-6 1-(2,5-Dimethoxy-4-methyl-phenyl)-ethanone 
• 678149-61-6 3-methyl-3-(2,5-dimethoxy-4-methylphenyl)-pent-4-enol 
• 109-92-2 ethyl vinyl ether 

Downstream Products

• 678149-55-8 5-methyl-5-(2,5-dimethoxy-4-methylphenyl)hepta-1,6-dien-3-ol 
• 678149-58-1 4-methyl-4-(2,5-dimethoxy-4-methylphenyl)cyclopent-2-enone 

Relevant academic research and scientific papers

Total synthesis of enokipodins A-D and cuparene-1 ,4-diol

A Claisen rearrangement and RCM reaction based sequence has been developed for total synthesis of the antifungal sesquiterpenes enokipodins A-D and cuparene-1 ,4-diol starting from 2,5-dimethoxy-4-methythydroquinone. Copyright

The First Total Synthesis of the Antimicrobial Sesquiterpenes (±)-Enokipodins A and B

Efficient first total synthesis of antimicrobial sesquiterpenes enokipodins A and B (1 and 2, respectively) and formal total synthesis of cuparene-1,4-diol (5) and cuparene-1,4-quinone (7) have been accomplished starting from 2,5-dimethoxy-4-methyl-acetop