226080-03-1

Upstream product

• 214060-10-3 (2S,3S,4R,5S,6R)-7-(tert-butyldiphenylsilyloxy)-3,5-<(S)-3,4-dimethoxybenzylidenedioxy>-2-methoxymethoxy-4,6-dimethyl-1-heptyl 2,2-dimethylpropanoate 
• 226079-68-1 (2S,3S,4R,5S,6S,7R,8E,10S)-11-hydroxy-3,5-<(S)-3,4-dimethoxybenzylidenedioxy>-2,7-bis(methoxymethoxy)-4,6,8,10-tetramethyl-8-undecen-1-yl 2,2-dimethylpropanoate 
• 226079-81-8 methyl (2R,3S,4R,5S,6R)-7-(tert-butyldiphenylsilyloxy)-3,5-<(S)-3,4-dimethoxybenzylidenedioxy>-2-methoxymethoxy-4,6-dimethylheptanoate 
• 226079-82-9 (S)-2-[(2S,4S,5R,6S)-6-[(R)-2-(tert-Butyl-diphenyl-silanyloxy)-1-methyl-ethyl]-2-(3,4-dimethoxy-phenyl)-5-methyl-[1,3]dioxan-4-yl]-2-methoxymethoxy-ethanol 
• 226080-00-8 2,2-Dimethyl-propionic acid (S)-2-[(2S,4S,5R,6S)-2-(3,4-dimethoxy-phenyl)-6-((E)-(1S,2R,5S)-2-methoxymethoxy-1,3,5-trimethyl-6-oxo-hex-3-enyl)-5-methyl-[1,3]dioxan-4-yl]-2-methoxymethoxy-ethyl ester 
• 226079-53-4 methyl (2R,3S,4R,5S,6R)-7-(tert-butyldiphenylsilyloxy)-2-hydroxy-3,5-<(S)-3,4-dimethoxybenzylidenedioxy>-4,6-dimethylheptanoate 
• 226079-84-1 2,2-Dimethyl-propionic acid (S)-2-[(2S,4S,5R,6S)-2-(3,4-dimethoxy-phenyl)-6-((R)-2-hydroxy-1-methyl-ethyl)-5-methyl-[1,3]dioxan-4-yl]-2-methoxymethoxy-ethyl ester 
• 226079-50-1 (2S,3S,4R,5S,6S)-6-formyl-3,5-<(S)-3,4-dimethoxybenzylidenedioxy>-2-methoxymethoxy-4-methyl-1-heptyl 2,2-dimethylpropanoate 
• 226079-51-2 (2E,4S)-5-(tert-butyldiphenylsilyloxy)-2-iodo-4-methyl-2-pentene 
• 226079-85-2 (S)-tert-butyl(4,4-dibromo-2-methylbut-3-en-1-yloxy)diphenylsilane 
• 226416-47-3 (4S)-5-(tert-butyldiphenylsilyloxy)-4-methyl-2-pentyne 
• 214060-19-2 methyl (2R,3S,4R,5S,6R)-7-(tert-butyldiphenylsilyloxy)-2,3-dihydroxy-5-(3,4-dimethoxybenzyloxy)-4,6-dimethylheptanoate 
• 214060-11-4 methyl (2E,4S,5R,6R)-7-(tert-butyldiphenylsilyloxy)-5-(3,4-dimethoxybenzyloxy)-4,6-dimethyl-2-heptenoate 
• 226079-78-3 (3S,4S,5R)-6-(tert-Butyl-diphenyl-silanyloxy)-4-(3,4-dimethoxy-benzyloxy)-3,5-dimethyl-hexane-1,2-diol 

Downstream Products

• 226079-49-8 (3S,4E,6R,7S,8S,9R,10S,11S)-12-triethylsilyloxy-8,10-<(S)-3,4-dimethoxybenzylidenedioxy>-6,11-bis(methoxymethoxy)-3,5,7,9-tetramethyl-4-dodecen-2-one 

Relevant academic research and scientific papers

Synthetic studies of the 18-membered antitumor macrolide, tedanolide. 3. Stereocontrolled synthesis of the C1-C12 part via a synthesis of the C1-C7 fragment by a mismatched but efficient sharpless dihydroxylation and its coupling with the C8-C11 fragment

The C1-C12 part (4) of tedanolide (1) was synthesized starting from methyl (R)-3-hydroxy-2-methylpropionate (11a) via a coupling between the C1- C7 aldehyde (6) and the C8-C11 iodoalkene (7a). For a synthesis of 6, a mismatched but highly efficient Sharpless dihydroxylation of the α,β- unsaturated ester (15) with AD-mix-α was successfully applied. Compound 7a was synthesized using hydrozirconation to the alkyne (32).