85608-26-0

Upstream product

• 85608-17-9 3-Dimethylamino-3-phenyl-propionic acid tert-butyl ester 
• 3585-33-9 lithium dimethylamide 

Downstream Products

• 1353585-50-8 (+)-3-N,N-dimethylamino-3-phenylpropanol L-tartaric acid salt 
• 82769-75-3 (S)-(+)-3-(dimethylamino)-3-phenyl-1-propanol 
• 81402-52-0 3-(dimethylamino)-3-phenylpropan-1-ol 
• 1071929-03-7 Dapoxetine hydrochloride 
• 119356-77-3 dapoxetine 
• 103-25-3 3-phenylpropanoic acid methyl ester 
• 100-52-7 benzaldehyde 
• 65-85-0 benzoic acid 
• 220438-13-1 methyl 3-(dimethylamino)-3-phenylpropionate 
• 506-59-2 N,N-dimethylammonium chloride 
• 621-82-9 Cinnamic acid 
• 131357-34-1 (S)-ethyl 3-N,N-dimethylamino-3-phenylpropanoate 

Relevant academic research and scientific papers

Assignment of the Absolute Configuration to Winterstein's Acid, R-3-Dimethylamino-3-phenyl Propionic Acid, by the Asymmetric Synthesis of Homochiral (S)-(+)-Ethyl 3-Dimethylamino-3-phenyl Propionate

The asymmetric synthesis of homochiral (S)-(+)-ethyl 3-dimethylamino-3-phenyl propionate, via stereoselective Michael addition of lithium dimethylamide to (S)-Z-5-C5H5)-Fe(CO)(PPh3)COCH=CHPh> and oxidative decomplexation, establishes the absolute configuration of Winterstein's acid 3-dimethylamino-3-phenyl propionic acid derived from Taxine B, as R.

Action d'organometalliques fonctionnels sur des gem-aminoethers et des sels d'immonium. I. Synthese d'amines α- ou β-fonctionnelles difficilement accessibles par reaction de Mannich

Some α- or β-functional amines which are difficult to obtain by Mannich reaction can be easily prepared from organomagnesium or organozinc functional derivatives and gem-aminoethers or immonium salts.