326471-52-7

Upstream product

• 1287289-17-1 C₃₂H₄₂O₅Si 
• 88159-03-9 5-(2,2-dimethyl-1,1-diphenyl-1-silapropoxy)pent-2-yn-1-ol 
• 127665-77-4 (E)-5-(2,2-dimethyl-1,1-diphenyl-1-silapropoxy)pent-2-en-1-ol 
• 88158-68-3 4-(tert-butyldiphenylsilyloxy)-1-butyne 

Downstream Products

• 1240380-55-5 (tert-butyl)({(3S)-3-[(4-methoxybenzyl)oxy]pent-4-en-1-yl}oxy)diphenylsilane 
• 1287289-22-8 C₂₉H₃₆O₄Si 
• 326471-47-0 (1S,3R,4S,5S)-4-Benzyloxy-1,5-bis-(tert-butyl-dimethyl-silanyloxy)-7-(tert-butyl-diphenyl-silanyloxy)-1-{(2S,3R)-3-[2-(4-methoxy-benzyloxy)-ethyl]-oxiranyl}-3-methyl-heptan-3-ol 
• 326471-67-4 (E)-(5S,7R,8S,9S)-8-Benzyloxy-9-(tert-butyl-dimethyl-silanyloxy)-11-(tert-butyl-diphenyl-silanyloxy)-1-(4-methoxy-benzyloxy)-7-methyl-7-trimethylsilanyloxy-undec-3-en-5-ol 
• 326471-48-1 (E)-(7R,8S,9S)-8-Benzyloxy-9-(tert-butyl-dimethyl-silanyloxy)-11-(tert-butyl-diphenyl-silanyloxy)-1-(4-methoxy-benzyloxy)-7-methyl-7-trimethylsilanyloxy-undec-3-en-5-one 
• 326471-69-6 (1S,3R,4S,5S)-4-Benzyloxy-5-(tert-butyl-dimethyl-silanyloxy)-7-(tert-butyl-diphenyl-silanyloxy)-1-{(2R,3R)-3-[2-(4-methoxy-benzyloxy)-ethyl]-oxiranyl}-3-methyl-heptane-1,3-diol 
• 326471-68-5 (E)-(5S,7R,8S,9S)-8-Benzyloxy-9-(tert-butyl-dimethyl-silanyloxy)-11-(tert-butyl-diphenyl-silanyloxy)-1-(4-methoxy-benzyloxy)-7-methyl-undec-3-ene-5,7-diol 
• 326471-66-3 (E)-(7R,8S,9S)-8-Benzyloxy-9-(tert-butyl-dimethyl-silanyloxy)-11-(tert-butyl-diphenyl-silanyloxy)-7-hydroxy-1-(4-methoxy-benzyloxy)-7-methyl-undec-3-en-5-one 
• 326471-49-2 [5-benzyloxy-6-(tert-butyl-dimethyl-silanyloxy)-8-(tert-butyl-diphenyl-silanyloxy)-4-methyl-2-oxo-4-trimethylsilanyloxy-octyl]-phosphonic acid dimethyl ester 
• 326471-53-8 [(3S,4R)-4-Benzyloxy-3-(4-methoxy-benzyloxy)-5-trityloxy-pentyloxy]-tert-butyl-diphenyl-silane 
• 326471-63-0 C₄₃H₇₂O₅Si₄ 
• 326471-61-8 4-benzyloxy-1,5-bis-(tert-butyl-dimethyl-silanyloxy)-7-(tert-butyl-diphenyl-silanyloxy)-3-methyl-heptan-3-ol 
• 326471-58-3 1-{(E)-(1S,2R)-2-Benzyloxy-5-(tert-butyl-dimethyl-silanyloxy)-1-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-3-methyl-pent-3-enyloxymethyl}-4-methoxy-benzene 
• 326471-64-1 4-benzyloxy-5-(tert-butyl-dimethyl-silanyloxy)-7-(tert-butyl-diphenyl-silanyloxy)-3-methyl-3-trimethylsilanyloxy-heptan-1-ol 

Relevant academic research and scientific papers

Total synthesis of achaetolide from D-mannitol

A highly convergent stereoselective total synthesis of achaetolide, a ten-membered lactone is described. The ring-closing metathesis reaction was used to construct the macrocycle and E-olefinic moiety in the molecule. The key acid and alcohol fragments we

Synthetic studies on pectenotoxins: Synthesis of the common C8-C18 THF fragment

The stereoselective synthesis of the common C8-C18 THF fragment of pectenotoxins is reported. The THF ring was constructed by the ring closure of the epoxide possessing all six asymmetric centers with a 5-exo-mode. These stereogenic centers were arranged successively from the enantiomerically active epoxide by utilizing the stereo-differentiating influence of the proximal functional groups.