169274-92-4

Upstream product

• 2579-22-8 Phenylpropargyl aldehyde 
• 35019-66-0 (4S,5S)-2,2-dimethyl-4-phenyl-1,3-dioxan-5-amine 

Downstream Products

• 147722-49-4 (-)-(S)-4-Phenylbut-3-in-2-ylamin 
• 147722-50-7 (+)-(S)-1-Phenylpent-1-in-3-ylamin 
• 169208-87-1 (-)-(S)-N-(4-Phenylbut-3-in-2-yl)formamid 
• 169208-88-2 (-)-(S)-N-(1-Phenylpent-1-in-3-yl)formamid 
• 763903-21-5 (-)-(1S,2S,3'S)-1-Phenyl-2-(1'-phenylpent-1'-in-3'-ylamino)propan-1,3-diol 
• 147722-51-8 (+)-(S)-1-Phenylhept-1-in-3-ylamin 
• 169208-89-3 (-)-(S)-N-(1-Phenylhept-1-in-3-yl)formamid 
• 751457-42-8 (-)-(1S,2S,2'S)-1-Phenyl-2-(4'-phenylbut-3'-in-2'-ylamino)propan-1,3-diol 
• 772315-74-9 (-)-(1S,2S,3'S)-1-Phenyl-2-(1'-phenylhept-1'-in-3'-ylamino)propan-1,3-diol 

Relevant academic research and scientific papers

Enantioselective Synthesis of Allyl- and Propargylamines via Nucleophilic 1,2-Addition to Chiral Aldimines

The asymmetric synthesis of allylamines and propargylamines 5 in high enantiomeric purity (e.e >/= 97percent) is described.Key step is the 1,2-addition of organocerium reagents to chiral α,β-unsaturated aldimines 3 to produce secondary amines 4.The chiral