105104-08-3

Upstream product

• 922-65-6 divinylcarbinol 
• 105104-05-0 4-acetoxy-5-bromo-2-methoxy-3-methylphenyl 2,4-pentadienyl ether 
• 105104-04-9 Acetic acid 6-bromo-4-formyl-3-methoxy-2-methyl-phenyl ester 
• 88088-57-7 4-acetoxy-5-bromo-2-methoxy-3-methylphenol 
• 105104-03-8 5-Bromo-4-hydroxy-2-methoxy-3-methyl-benzaldehyde 
• 88010-46-2 6-Bromo-3-methoxy-2-methyl-phenol 
• 40596-30-3 penta-2,4-dienyl chloride 
• 100-39-0 benzyl bromide 
• 105104-06-1 6-bromo-3-methoxy-2-methyl-4-<(2,4-pentadienyl)oxy>phenyl 

Downstream Products

• 105104-31-2 4-(benzyloxy)-3-bromo-6-methoxy-5-methyl-2-(2,4-pentadienyl)phenol 

Relevant academic research and scientific papers

Lewis Acid Mediated Claisen-Type Rearrangement of Aryl Dienyl Ethers

Rearrangement of aryl pentadienyl ethers in the presence of BF3*OEt2 affords pentadienyl phenols in good yields without formation of the corresponding rearranged products.The mechanism of this rearrangement was studied by deuterium labeling and cross-coupling reactions.The scope and limitations of the rearrangement are discussed.