197219-40-2

Upstream product

• 5390-04-5 pent-1-yn-5-ol 
• 197219-37-7 (5E)-9-(4-methoxybenzyloxy)-1-(oxan-2-yloxy)-5-nonen-2-yne 
• 197219-38-8 (5E)-9-(4-methoxybenzyloxy)-5-nonen-2-yn-1-ol 
• 197219-15-1 6-[(4-methoxyphenyl)methoxy]-2-hexyn-1-ol 
• 197219-35-5 6-[(4-methoxyphenyl)methoxy]-(E)-2-hexen-1-ol 
• 197219-36-6 (2E)-1-bromo-6-(4-methoxybenzyloxy)-2-hexene 
• 197219-01-5 1-methoxy-4-pent-4-ynyloxymethyl-benzene 
• 824-94-2 p-methoxybenzyl chloride 
• 197219-39-9 (2E,5E)-9-(4-methoxybenzyloxy)-2,5-nonadien-1-ol 

Downstream Products

• 197219-43-5 (7S,8S,4E)-1-bromo-9-(tert-butyldiphenylsilyloxy)-7,8-epoxy-4-nonene 
• 197219-49-1 (4S,5S,7S,8S)-1-bromo-9-(tert-butyldiphenylsilyloxy)-4,5,7,8-diepoxynonane 
• 197219-44-6 (4R,5R,7S,8S)-1-bromo-9-(tert-butyldiphenylsilyloxy)-4,5,7,8-diepoxynonane 
• 197219-47-9 (S)-2-(tert-Butyl-diphenyl-silanyloxy)-1-(2R,3aR,7aS)-hexahydro-furo[3,2-b]pyran-2-yl-ethanol 

Relevant academic research and scientific papers

The biomimetic construction of fused cyclic polyethers

The formation of fused cyclic ethers by biomimetic synthesis was demonstrated. The one-pot successive ring-expansion reactions of bromo diepoxides were investigated by regarding the epoxy groups as the nucleophiles for the intramolecular cationic carbons to obtain the fused cyclic ethers.