147973-87-3

Upstream product

• 147973-76-0 (3S,7R,5Z)-7-benzyloxy-2-methylundeca-5,10-dien-3-ol 
• 147973-81-7 (5R,9S,6Z)-5,9-dibenzyloxy-10-methylundec-6-en-1-ol 
• 147973-82-8 (5R,9S,6Z)-5,9-dibenzyloxy-10-methylundec-6-enal 
• 147973-80-6 (5R,9S,6Z)-5,9-dibenzyloxy-10-methylundeca-1,6-diene 
• 147973-72-6 S-methyl O-(4R,2E)-4-benzyloxyocta-2,7-dien-1-yl dithiocarbonate 
• 147973-79-3 (7R,5Z)-7-benzyloxy-2-methylundeca-5,10-dien-3-one 
• 147973-69-1 (R)-2-benzyloxyhex-5-enal 
• 83861-87-4 (2R)-2-(benzyloxy)-5-hexen-1-ol 
• 133494-68-5 (R)-1,2-dihydroxy-5-hexene 
• 1125-88-8 benzaldehyde dimethyl acetal 

Downstream Products

• 147973-88-4 (5R,9R,13R,17S,6Z,14Z)-18-methyl-5,9,13,17-tetrabenzyloxynonadeca-6,14-dienal 
• 147973-86-2 (5R,9R,13R,17S,6Z,14Z)-18-methyl-5,13,17-tribenzyloxynonadeca-1,6,14-trien-9-ol 

Relevant academic research and scientific papers

Stereoselective Synthesis of Aliphatic 1,5,9,13-Polyols using (δ-Alkoxyallyl)stannanes

Treatment of aliphatic aldehydes with the allyltin trichloride generated from the 4-benzyloxyocta-2,7-dienylstannane 18 and tin(IV)chloride provides stereoselective access to polyhydroxylated compounds with the hydroxyl groups at positions 1,5,9,13- etc.