333969-68-9

Upstream product

• 100-39-0 benzyl bromide 
• 496841-04-4 methyl (2S,3S)-3-hydroxypyrrolidine-2-carboxylate 

Downstream Products

• 1374647-68-3 [(2R,3S)-1-benzyl-3-(tert-butyldiphenylsilyloxy)pyrrolidin-2-yl]methanol 
• 1374647-70-7 (2R,3S)-2-(azidomethyl)-1-benzyl-3-(tert-butyldiphenylsilyloxy)pyrrolidine 
• 1374647-71-8 methyl (2S,3R)-3-azido-1-benzylpyrrolidine-2-carboxylate 
• 1024021-36-0 tert-butyl [(2S,3R)-1-Benzyl-2-(hydroxymethyl)pyrrolidin-3-yl]carbamate 
• 1374647-72-9 tert-butyl [(2R,3R)-2-(azidomethyl)-1-benzylpyrrolidin-3-yl]carbamate 
• 1374647-69-4 methyl (2S,3S)-1-benzyl-3-(tert-butyldiphenylsilyloxy)pyrrolidine-2-carboxylate 

Relevant academic research and scientific papers

Access to optically active 3-aminopiperidines by ring expansion of prolinols: Thermodynamic versus kinetic control

3-Aminopiperidines are of great interest because they can possess a wide range of biological activity depending on the nitrogen substituents. Different approaches their synthesis are presented and the most efficient is a ring expansion of prolinols induce