401895-10-1

Upstream product

• 149520-42-3 3-(4-methoxyphenyl)-but-2-en-1-ol 
• 1712-69-2 1-isopropenyl-4-methoxybenzene 
• 75749-89-2 1-Methoxy-4-(1-methyl-cyclobut-2-enyl)-benzene 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 401895-09-8 C₂₆H₃₂O₂ 
• 401895-11-2 C₁₉H₂₂N₂O₃S 
• 401895-13-4 toluene-4-sulfonic acid 3-(4-methoxy-phenyl)-3-methyl-cyclobutyl ester 
• 401895-12-3 3-(4-methoxy-phenyl)-3-methyl-cyclobutanol 
• 460323-49-3 2-(4-methoxy-phenyl)-2-methyl-5-methylene-cyclopentanol 
• 460323-47-1 1-(1,3-dimethyl-cyclopent-2-enyl)-4-methoxy-benzene 
• 460323-46-0 (E)-5-(4-Methoxy-phenyl)-hex-3-en-2-one 
• 34399-55-8 5-(4-methoxy-phenyl)-hexan-2-one 
• 50415-73-1 methyl 2-(4-methoxyphenyl)propionate 
• 23786-14-3 4-methoxy-phenyl acetic acid methyl ester 

Downstream Products

• 223691-88-1 1-(1,5-dimethyl-1-vinyl-hex-4-enyl)-4-methoxy-benzene 
• 349473-22-9 4-(5,7-dimethylocta-1,6-dien-4-yl)phenol 
• 223691-84-7 4-(4-methoxyphenyl)-4-methyl-hex-5-en-1-al 

Relevant academic research and scientific papers

Synthesis of sporochnol A, a marine fish deterrent

A synthesis of the methyl ether of the fish-deterrent sporochnol A is described. The route involves the application of Claisen ortho-ester rearrangement to generate the key quaternary carbon. Copyright Taylor & Francis, Inc.

Total synthesis of sporochnols, fish deterrents from a marine alga

Sporochnols, fish deterrents from a marine alga, were synthesized, using intramolecular C-H insertion of alkylidenecarbene as a key step to construct the chiral quaternary center.

Employment of a cyclobutene ring-opening metathesis reaction towards a concise synthesis of (±)-sporochnol A

A concise formal synthesis of (±)-sporochnol A 1, a naturally occurring feeding deterrent towards herbivorous fish, is described. The target compound was prepared by the employment of a Ru-catalysed cyclobutene ring-opening metathesis reaction with gaseou