439587-54-9

Upstream product

• 153924-63-1 β-[(phenylmethylene)amino]-[R-(E)-]-benzeneethanol 
• 100-52-7 benzaldehyde 
• 24424-99-5 di-tert-butyl dicarbonate 
• 132313-03-2 (2R)-2-phenyl-2-[(1'R)-1'-phenylbut-3'-enylamino]ethanol 

Downstream Products

• 1345893-93-7 tert-butyl (R)-5-(3-chlorophenyl)-5-oxo-1-phenylpentylcarbamate 
• 1345893-95-9 tert-butyl (R)-5-cyclopropyl-5-oxo-1-phenylpentylcarbamate 
• 1345893-92-6 tert-butyl (R)-5-oxo-1,5-diphenylpentylcarbamate 
• 1345893-94-8 tert-butyl (R)-5-(2-bromophenyl)-5-oxo-1-phenylpentylcarbamate 
• 1345893-96-0 tert-butyl (R)-7-methyl-5-oxo-1-phenyloctylcarbamate 
• 1345894-09-8 (2R,6R)-2-allyl-2,6-diphenylpiperidine 
• 1345894-10-1 (5R,8aR)-5,8a-diphenyl-octahydroindolizine 
• 1345894-01-0 (2S,6R)-2-(3-chlorophenyl)-6-phenylpiperidine 
• 1345894-02-1 (2S,6R)-2-(2-bromophenyl)-6-phenylpiperidine 
• 1345894-03-2 (2S,6R)-2-cyclopropyl-6-phenylpiperidine 
• 1345894-04-3 (2S,6R)-2-isobutyl-6-phenylpiperidine 
• 38047-66-4 (2R,6S)-2,6-diphenylpiperidine 

Relevant academic research and scientific papers

Indium-mediated asymmetric barbier-type allylation of aldimines in alcoholic solvents: Synthesis of optically active homoallylic amines

(Chemical Equation Presented) Chiral aldimines derived from phenylglycinol were diastereoselectively allylated with indium powder/allyl bromide in alcoholic solvents. Both aliphatic and aromatic aldimines provided good yield of the desired products with h