171196-76-2

Upstream product

• 171196-81-9 ethyl (R,Z)-4-(N-α-methylbenzylamino)-2-butenoate 
• 3886-69-9 (R)-1-phenyl-ethyl-amine 
• 126275-19-2 (R)-N-allyl (1-phenylethyl)amine 

Downstream Products

• 228555-90-6 ethyl (3S,4R,1'R,1''S)-<3-(1''-hydroxyethyl)-2-oxo-1-(1'-phenylethyl)pyrrolidin-4-yl>acetate 
• 228555-91-7 ethyl (3S,4R,1'R,1''R)-<3-(1''-hydroxyethyl)-2-oxo-1-(1'-phenylethyl)pyrrolidin-4-yl>acetate 
• 224645-98-1 ethyl (3S,4R,1'R)-<3-acetyl-2-oxo-1-(1'-phenylethyl)pyrrolidin-4-yl>acetate 
• 228556-01-2 ethyl (3S,4R,1'R,1''S)-<3-(1''-methanesulphonyloxyethyl)-2-oxo-1-(1'-phenylethyl)pyrrolidin-4-yl>acetate 
• 224645-96-9 (E,R)-N-(3-ethoxycarbonyl-2-propenyl)-N-(1-phenylethyl)-3-oxobutanamide 

Relevant academic research and scientific papers

Diastereoselective Preparation of Chiral Lithiated Allyl Amines: Application in EPC-Synthesis

Lithiation of chiral allylamine (R)-1 with BunLi and ButLi leads to the formation of intermediate (R)-2, which by reaction with D2O, Me2CO or (CH2)5CO affords the expected chiral compounds (R)-3, (R)-4 and (R)-5, respectively.With Bu