369362-38-9

Upstream product

• 433732-71-9 3-(2,3-dimethoxy-5-methyl-phenyl)-3-methyl-pent-4-enal 
• 369362-35-6 2-(2,3-dimethoxy-5-methyl-phenyl)-2-methyl-pent-4-enoic acid methyl ester 
• 369362-36-7 2-(2,3-dimethoxy-5-methyl-phenyl)-2-methyl-pent-4-enal 
• 96202-91-4 (2,3-dimethoxy-5-methyl-phenyl)-acetic acid methyl ester 
• 369362-34-5 2-(2,3-dimethoxy-5-methyl-phenyl)-propionic acid methyl ester 
• 93-51-6 2-Methoxy-4-methylphenol 
• 433732-68-4 (E)-3-(2,3-Dimethoxy-5-methyl-phenyl)-but-2-en-1-ol 
• 433732-77-5 4-(2,3-dimethoxy-5-methyl-phenyl)-4-methyl-cyclopent-2-enol 
• 369362-37-8 2-(2,3-dimethoxy-5-methyl-phenyl)-2-methyl-4-oxo-pentanal 
• 433732-66-2 (E)-3-(2,3-Dimethoxy-5-methyl-phenyl)-but-2-enoic acid ethyl ester 
• 121-33-5 vanillin 
• 369362-33-4 (2,3-dimethoxy-5-methyl-phenyl)-acetaldehyde 
• 201359-55-9 1-(allyloxy)-2-methoxy-4-methylbenzene 
• 369362-32-3 1-allyl-2,3-dimethoxy-5-methyl-benzene 

Relevant academic research and scientific papers

A ring closing metathesis-based approach to (±)-herbertene, (±)-α-herbertenol, (±)-β-herbertenol and (±)-herbertenediol

An efficient methodology for the synthesis of the aromatic sesquiterpenes (±)-herbertene, (±)-α-herbertenol, (±)-β-herbertenol (±)-herbertenediol and (±)-α-cuparenone, employing a combination of Claisen rearrangement and ring closing metathesis reactions,

Formal total synthesis of (±)-herbertenediol and (±)-mastigophorenes A and B

A simple and straightforward formal total synthesis of the sesquiterpene herbertenediol and its dimers mastigophorenes A and B, starting from vanillin, is described.