344796-28-7

Upstream product

• 344796-30-1 tert-Butyl-{(1S,2S)-1-[(S)-1-(4-methoxy-benzyloxy)-ethyl]-2-methyl-but-3-enyloxy}-dimethyl-silane 

Downstream Products

• 344796-32-3 (3R,4R,5S,6S,7S)-6-(tert-Butyl-dimethyl-silanyloxy)-7-(4-methoxy-benzyloxy)-3,5-dimethyl-oct-1-en-4-ol 
• 344796-33-4 (3S,4R,5S,6S,7S)-6-(tert-Butyl-dimethyl-silanyloxy)-7-(4-methoxy-benzyloxy)-3,5-dimethyl-oct-1-en-4-ol 
• 1196-00-5 (+)-isopinocampheol 
• 344796-38-9 1-[(1S,2S,3S,4R,5R)-2-(tert-Butyl-dimethyl-silanyloxy)-1,3,5-trimethyl-4-triethylsilanyloxy-hept-6-enyloxymethyl]-4-methoxy-benzene 

Relevant academic research and scientific papers

Synthetic studies of antitumor natural products superstolides A and B. Construction of C20-C26 fragment of superstolide A.

[structure: see text] The C20-C26 portion of the antitumor macrolide superstolide A was synthesized by employing Brown's asymmetric crotylboronate methodology.

Improved procedure for the oxidative cleavage of olefins by OsO 4-NaIO4

(Chemical Equation Presented) Oxidative cleavage of olefins by OsO 4-NaIO4 sometimes suffers from low yields due to the formation of side products. It is found that the addition of 2,6-lutidine can suppress the side reactions and dra