143326-16-3

Upstream product

• 183888-76-8 (S)-4-{(1S)-2-[(1,1-dimethylethyl)diphenylsilyloxy]-1-(phenylmethoxy)ethyl}-2,2-dimethyl-1,3-dioxolane 
• 183888-74-6 (S)-4-{(1S)-2-[(1,1-dimethylethyl)diphenylsilyloxy]-1-(hydroxy)ethyl}-2,2-dimethyl-1,3-dioxolane 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 100-39-0 benzyl bromide 

Downstream Products

• 183888-77-9 (2S,3S)-(+)-3-benzyloxy-1,4-bis(tert-butyl-diphenyl-silyloxy)butan-2-ol 
• 1004972-62-6 (S)-3-[(1,1-dimethylethyl)diphenylsilyloxy]-2-(phenylmethoxy)propanal 
• 183888-69-9 (3R)-3-benzyloxy-1,4-bis(tert-butyl-diphenyl-silyloxy)butan-2-one 

Relevant academic research and scientific papers

Anti aldol selectivity in a synthetic approach to the C1-C 12 fragment of the tedanolides

In a synthetic approach to the completely protected C1 C 12 fragment of the macrocyclic cytotoxic agent tedanolide 1, we carried out the tin-catalyzed Mukaiyama aldol reaction between the 2,3-dialkoxypropanal 5 and the silyl enol eth

Synthesis of protected enantiopure erythrulose derivatives

D- and L-Erythrulose derivatives 2-6 bearing protective O-silyl and O-benzyl groups in various positions were synthesized in enantiopure form from L-ascorbic acid, D-isoascorbic acid, and D-glucose. VCH Verlagsgesellschaft mbH, 1996.