94142-51-5

Upstream product

• 74-88-4 methyl iodide 

Downstream Products

• 191212-44-9 (2R,4R)-1-benzyloxy-4-(4-methoxyphenyl)-4-methyl-5-hexen-2-ol 
• 191212-48-3 (R)-5-(4-Methoxy-phenyl)-5-methyl-hept-6-enoic acid methyl ester 
• 191212-47-2 (E)-(R)-5-(4-Methoxy-phenyl)-5-methyl-hepta-2,6-dienoic acid methyl ester 
• 191212-49-4 (R)-6-(4-methoxyphenyl)-2,6-dimethyl-7-octen-2-ol 
• 191212-45-0 (2R,4R)-4-(4-methoxyphenyl)-4-methyl-5-hexene-1,2-diol 
• 191212-50-7 (R)-1-(3,7-dimethylocta-1,6-dien-3-yl)-4-methoxybenzene 
• 191212-51-8 1-Methoxy-4-((E)-(R)-4-methoxy-1-methyl-1-vinyl-but-3-enyl)-benzene 
• 191212-52-9 (R)-(-)-4-(4-methoxyphenyl)-4-methylhex-5-en-1-al 
• 191212-46-1 (R)-3-(4-methoxyphenyl)-3-methyl-4-pentenal 
• 223692-13-5 (3S,5R)-5-Benzyloxymethyl-3-(4-methoxy-phenyl)-3-methyl-tetrahydro-furan-2-ol 

Relevant academic research and scientific papers

The absolute configuration of (+)-sporochnol A, the fish deterrent from the Caribbean marine alga Sporochnus bolleanus

The absolute configuration of (+)-sporochnol A, the fish deterrent from the Caribbean marine alga Sporochnus bolleanus, has been established as S based on the stereocontrolled synthesis of its (R)-(-)-enantiomer from (S)-epichlorohydrin.