858128-75-3

Upstream product

• 676608-43-8 methyl 2-(2-methoxy-5-methylphenyl)pent-4-enoate 
• 676608-51-8 methyl (2-methoxy-5-methylphenyl)acetate 
• 556-82-1 3-methyl-2-buten-1-ol 
• 858128-73-1 3-methylbut-2-enyl 2-(2-methoxy-5-methylphenyl)pent-4-enoate 
• 75-77-4 chloro-trimethyl-silane 

Downstream Products

• 815620-64-5 [1-(2'-methoxy-5'-methylphenyl)-2,2-dimethylcyclopentyl]-methanol 
• 603985-16-6 methyl 1-(2-methoxy-5-methylphenyl)-2,2-dimethylcyclopentane-carboxylate 
• 603985-12-2 1-(2-methoxy-5-methyl-phenyl)-2,2-dimethyl-cyclopentanecarbaldehyde 
• 220106-58-1 1-methoxy-4-methyl-2-(1,2,2-trimethylcyclopentyl)-benzene 
• 858128-76-4 methyl 2-allyl-3,3-dimethyl-2-(2-methoxy-5-methylphenyl)pent-4-enoate 
• 858128-77-5 methyl 2,2-dimethyl-1-(2-methoxy-5-methylphenyl)cyclopent-3-enecarboxylate 

Relevant academic research and scientific papers

Formal total synthesis of (±)-herbertene-1,13-diol and (±)-α-herbertenol via Ireland ester Claisen rearrangement and RCM reaction sequence

A combination of Ireland ester Claisen rearrangement and ring-closing metathesis (RCM) reactions has been employed for efficient formal total syntheses of herbertene-1,13-diol and α-herbertenol, sesquiterpenes containing two vicinal quaternary carbon atom