182479-52-3

Upstream product

• 182479-47-6 tert-Butyl-((E)-3-iodo-1,2-dimethyl-allyloxy)-diphenyl-silane 
• 182479-37-4 (E)-4-iodo-3-methylbut-3-en-2-ol 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 3020-28-8 (iodomethyl)triphenylphosphonium iodide 
• 182479-49-8 (E)-4-(tert-Butyl-diphenyl-silanyloxy)-3-methyl-pent-2-enal 

Downstream Products

• 182479-32-9 (3E,5Z,7E)-3-Methyl-8-phenyl-octa-3,5,7-trien-2-ol 
• 125010-17-5 lignarenone B 
• 125010-16-4 lignarenone A 

Relevant academic research and scientific papers

Stereoselective synthesis of polyenic alarm pheromones of cephalaspidean molluscs

The stereospecific thallium-accelerated palladium-catalyzed cross- coupling of 1-alkenyl boronic acids and 1-alkenyl iodides (the Suzuki reaction) is the key step in an efficient approach to several polyenic pheromones isolated from cephalaspidean opisthobranch molluscs.