1429183-75-4

Upstream product

• 1315158-32-7 tert-butyl (2R,3R)-3-(tert-butyldiphenylsilyloxy)-1-oxopent-4-en-2-ylcarbamate 
• 1020409-56-6 tert-butyl (2S,3R)-3-(tert-butyldiphenylsilyloxy)-1-hydroxypent-4-en-2-ylcarbamate 
• 1315158-29-2 tert-butyl (S)-4-[(R)-1-(tert-butyldiphenylsilyloxy)allyl]-2,2-dimethyloxazolidine-3-carboxylate 
• 1429183-74-3 tert-butyl (1S,2S,3S,4S,6R)-2-(tert-Butyldiphenylsilyloxy)-3,4,6-trihydroxycyclohexylcarbamate 
• 1429183-73-2 tert-butyl (1S,2R,6R)-2-(tert-butyldiphenylsilyloxy)-6-hydroxycyclohex-3-enylcarbamate 
• 114301-34-7 tert-butyl (S)-4-((R)-1-hydroxyallyl)-2,2-dimethyloxazolidine-3-carboxylate 
• 114301-34-7 (2S,3S)-2-amino-N-<(tert-butyloxy)carbonyl>-1,3-dihydroxy-1,2-O,N-isopropylidene-4-pentene 
• 1429183-69-6 tert-butyl (3R,4S,5R)-3-(tert-butyldiphenylsilyloxy)-5-hydroxyocta-1,7-dien-4-ylcarbamate 

Relevant academic research and scientific papers

Diversity-oriented synthesis of aminocyclohexitols from Garner's aldehyde

A short and efficient synthetic route to three stereoisomeric aminocyclohexane tetrols of the quercitol type has been developed from l-serine, which featured stereoselective allylation, stereocontrolled dihydroxylation, and ring-closing metathesis as key steps. Georg Thieme Verlag Stuttgart · New York.