79561-72-1

Upstream product

• 2577-90-4 methyl (2S)-2-amino-3-phenylpropanoate 
• 106-95-6 allyl bromide 
• 7524-50-7 methyl (2S)-2-amino-3-phenylpropanoate hydrochloride 

Downstream Products

• 2577-90-4 methyl (2S)-2-amino-3-phenylpropanoate 
• 890657-45-1 2-diallylamino-3-phenyl-propionic acid N'-phenyl-hydrazide 
• 116763-08-7 methyl (S)-3-phenyl-2-(1H-pyrrol-1-yl)propanoate 
• 847899-98-3 (S)-methyl 2-(2,5-dihydro-1H-pyrrol-1-yl)-3-phenylpropanoate 

Relevant academic research and scientific papers

Synthesis of enantiomerically pure (+)- and (-)-protected 5-aminomethyl-1,3-oxazolidin-2-one derivatives from allylamine and carbon dioxide

The stereoselective synthesis of enantiomerically pure (5R)- and (5S)-aminomethyl-oxazolidinones with different protecting groups have been carried out from an allyl amine as the source of the carbon backbone. The key reaction is the high yield iodiocyclization of enantiomerically pure allylphenethyl amine in the presence of carbon dioxide.

Lewis acid assisted ring-closing metathesis of chiral diallylamines: An efficient approach to enantiopure pyrrolidine derivatives

(Chemical Equation Presented) Lewis acid assisted ring-closing olefin metathesis (RCM) of chiral diallylamines, using the second generation RCM ruthenium-based catalyst, leads to enantiopure pyrrolidine derivatives in 79-93% yields under very mild conditi

A NEW PROTECTING GROUP FOR AMINES. SYNTHESIS OF ANTICAPSIN FROM L-TYROSINE

An acid and base-stable, nucleophile-resistant protecting group for primary amines and α-amino acids is described which has been used in a synthesis of the title compound.