1618679-31-4

Upstream product

• 100-39-0 benzyl bromide 

Downstream Products

• 1175524-30-7 tert-butyl (2S,3R)-3-(benzyloxy)-1-hydroxypentan-2-ylcarbamate 
• 1618679-32-5 tert-butyl (3R,4S,E)-3,8-bis(benzyloxy)oct-5-en-4-ylcarbamate 
• 1618679-34-7 (4S,5R,E)-ethyl 5-(benzyloxy)-4-(tert-butoxycarbonylamino)hept-2-enoate 
• 1618679-38-1 C₂₁H₃₃NO₅ 
• 1618679-35-8 tert-butyl (4S,5R)-5-(benzyloxy)-1-hydroxyheptan-4-ylcarbamate 
• 1618679-36-9 (S)-tert-butyl 2-((R)-1-(benzyloxy)propyl)pyrrolidine-1-carboxylate 

Relevant academic research and scientific papers

Formal synthesis of (+)-α-conhydrine and stereoselective synthesis of pyrrolidine analogue via the diastereoselective chelation-controlled hydride reduction and wittig reaction

Asymmetric syntheses of (+)-α-conhydrine and its pyrrolidine analogue were achieved from readily available L-serine. The key step involved highly diastereoselective chelation-controlled hydride reduction of the amino ketone to give the anti-amino alcohol