1320344-52-2

Upstream product

• 232280-22-7 methyl (2R)-2-methyl-3-[(1,1,1-triisopropylsilyl)oxy]propanoate 
• 171231-73-5 (2S,3S,4R,5S,6S)-5-(benzyloxy)-2,4,6-trimethylheptane-1,3,7-triol 
• 13154-24-0 triisopropylsilyl chloride 
• 1320344-47-5 (4S,5S)-4-[(1S,2S,3S)-2-(benzyloxy)-4-(methoxymethoxy)-1,3-dimethylbutyl]-2-(4-methoxyphenyl)-5-methyl-1,3-dioxan 
• 1320344-51-1 (2R,3R,6S,7S,8R,9S,10S)-9-(benzyloxy)-7-[(4-methoxybenzyl)oxy]-11-(methoxymethoxy)-2,6,8,10-tetramethyl-1-[(1,1,1-triisopropylsilyl)oxy]-4-undecan-3-ol 
• 1320344-45-3 C₂₇H₃₈O₆ 
• 1320344-48-6 (2S,3S,4R,5S,6S)-5-(benzyloxy)-3-[(4-methoxybenzyl)oxy]-7-(methoxymethoxy)-2,4,6-trimethylheptan-1-ol 
• 1204595-67-4 (2S,3S,4S)-3-(benzyloxy)-4-[(4S,5S)-2-(4-methoxyphenyl)-5-methyl-1,3-dioxan-4-yl]-2-methylpentan-1-ol 

Downstream Products

• 1320344-44-2 ({(2R)-2-(2S,5S,6S)-6-[(1S,2S,3S)-2-(benzyloxy)-4-(methoxymethoxy)-1,3-dimethylbutyl]-5-methyltetrahydro-2H-2-pyranylpropyl}oxy)(triisopropyl)silane 

Relevant academic research and scientific papers

Stereoselective synthesis of the C1-C11 tetrahydropyran core unit of (+)-zincophorin

Synthesis of the C1-C11 tetrahydropyran core unit of (+)-zincophorin using a desymmetrization strategy is reported. Horner-Wadsworth-Emmons (HWE) and Mitsunobu cyclization reactions are the key transformations. Georg Thieme Verlag Stuttgart - New York.