182479-32-9

Upstream product

• 6783-05-7 trans-2-phenylvinylboronic acid 
• 182479-23-8 (3E,5Z)-6-Iodo-3-methyl-hexa-3,5-dien-2-ol 
• 182479-37-4 (E)-4-iodo-3-methylbut-3-en-2-ol 
• 182479-47-6 tert-Butyl-((E)-3-iodo-1,2-dimethyl-allyloxy)-diphenyl-silane 
• 182479-49-8 (E)-4-(tert-Butyl-diphenyl-silanyloxy)-3-methyl-pent-2-enal 
• 182479-52-3 tert-Butyl-((2E,4Z)-5-iodo-1,2-dimethyl-penta-2,4-dienyloxy)-diphenyl-silane 

Downstream Products

• 125010-16-4 lignarenone A 
• 125010-17-5 lignarenone B 

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.