1339950-30-9

Upstream product

• 114301-34-7 (2S,3S)-2-amino-N-<(tert-butyloxy)carbonyl>-1,3-dihydroxy-1,2-O,N-isopropylidene-4-pentene 
• 1339950-28-5 tert-butyl N-[(5S,6S)-10,10-dimethyl-9,9-diphenyl-5-vinyl-2,4,8-trioxa-9-silaundecan-6-yl]carbamate 
• 106-95-6 allyl bromide 
• 1042338-92-0 (1S,2S)-(1-hydroxymethyl-2-methoxymethoxy-but-3-enyl)-carbamic acid tert-butyl ester 
• 1042338-78-2 (1S,4S)-4-(1-methoxymethoxyallyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester 

Downstream Products

• 1339950-32-1 tert-butyl (5S,6S)-6-[(tert-butyldiphenylsilyloxy)methyl]-5-(methoxymethoxy)-5,6-dihydropyridine-1(2H)-carboxylate 
• 305838-49-7 tert-butyl (2S,3S)-2-[(tert-butyldiphenylsilyloxy)methyl]-3-(methoxymethoxy)piperidine-1-carboxylate 

Relevant academic research and scientific papers

A stereoselective route to cis-(2S,3R)-3-hydroxypipecolic acid and two enantiomeric cis-2-hydroxymethyl-3-hydroxypiperidine derivatives

Stereoselective routes to cis-(2S,3R)-3-hydroxypipecolic acid and two enantiomeric cis-2-hydroxymethyl-3-hydroxypiperidine derivatives from a common precursor have been developed, which featured stereocontrolled vinylation of a -chiral aldehyde and ring-closing metathesis as key steps. Georg Thieme Verlag Stuttgart. New York.