862982-78-3

Upstream product

• 149520-42-3 3-(4-methoxyphenyl)-but-2-en-1-ol 
• 132533-07-4 (E)-3-(4-methoxyphenyl)but-2-ene-1-ol 
• 108454-55-3 3-(4-methoxyphenyl)-2-butenoic acid ethyl ester 
• 862982-44-3 ethyl 3-(4-methoxyphenyl)-3-methylpent-4-enoate 

Downstream Products

• 863093-00-9 toluene-4-sulfonic acid 3-(4-methoxy-phenyl)-3-methyl-pent-4-enyl ester 
• 863092-96-0 4-(4-methoxyphenyl)-4-methyl-hex-5-enonitrile 
• 863092-97-1 4-(4-methoxyphenyl)-4-methyl-hex-5-enoic acid 
• 401895-10-1 4-(4-methoxy-phenyl)-4-methyl-hex-5-en-1-ol 
• 223691-88-1 1-(1,5-dimethyl-1-vinyl-hex-4-enyl)-4-methoxy-benzene 
• 223691-84-7 4-(4-methoxyphenyl)-4-methyl-hex-5-en-1-al 
• 223691-80-3 1-methoxy-4-(4-methoxyphenyl)-4-methylhexa-1,5-diene 

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.

Synthetic approaches to sporochnols A-C

Formal total synthesis of sporochnols A-C, hydroxyphenyl substituted monoterpenes isolated from the Caribbean brown alga Sporochnus bolleanus exhibiting feeding deterrent property toward herbivorous fish, is described. Copyright Taylor & Francis, Inc.