849411-91-2

Upstream product

• 724422-95-1 dimethyl 3-{(1S)-1-[(1S)-1-benzyloxy-2-methoxymethoxyethyl]-6-(tert-butyldiphenylsilanyloxy)-1,5-dimethylhexyloxy}-2-oxopropylphosphonate 
• 849411-97-8 {3-[(S)-1-((R)-1-Benzyloxy-2-hydroxy-ethyl)-6-(tert-butyl-diphenyl-silanyloxy)-1,5-dimethyl-hexyloxy]-2-oxo-propyl}-phosphonic acid dimethyl ester 
• 1026615-09-7 {3-[(S)-1-((S)-1-Benzyloxy-2-oxo-ethyl)-6-(tert-butyl-diphenyl-silanyloxy)-1,5-dimethyl-hexyloxy]-2-oxo-propyl}-phosphonic acid dimethyl ester 
• 849411-96-7 ethyl {(1R)-1-[(1R)-1-benzyloxy-2-methoxymethoxyethyl]-6-(tert-butyldiphenylsilanyloxy)-1,5-dimethylhexyloxy}acetate 
• 849411-90-1 ethyl (2S,3S)-2-benzyloxy-8-(tert-butyldiphenylsilanyloxy)-3-hydroxy-3,7-dimethyloctanoate 
• 724422-94-0 (2R,3S)-2-benzyloxy-8-(tert-butyldiphenylsilanyloxy)-1-methoxymethoxy-3,7-dimethyloctan-3-ol 
• 849411-95-6 (2R,3S)-2-benzyloxy-8-(tert-butyldiphenylsilanyloxy)-3,7-dimethyloctane-1,3-diol 
• 724422-93-9 (2S,3S)-ethyl 8-(tert-butyldiphenylsilanyloxy)-2,3-dihydroxy-3,7-dimethyloctanoate 
• 724422-92-8 (Z)-ethyl 8-(tert-butyldiphenylsilanyloxy)-3,7-dimethyloct-2-enoate 
• 144693-95-8 tert-butyldipheny((2-methylpent-4-en-1-yl)oxy)silane 
• 5673-98-3 2-methylpent-4-en-1-ol 
• 1575-74-2 (+-)-2-methyl-pent-4-enoic acid 

Relevant academic research and scientific papers

Synthetic approaches and total synthesis of natural zoapatanol

(Chemical Equation Presented) The total synthesis of (+)-zoapatanol utilizing an intramolecular Horner-Wadsworth-Emmons olefination and an enantioselective Sharpless dihydroxylation as the key steps has been achieved. An advanced oxepene intermediate has been obtained by applying a ring-closing metathesis to an unsaturated enol ether.