144632-41-7

Upstream product

• 34713-70-7 2-Phenylpropanal 
• 2133-40-6 L-proline methyl ester monohydrochloride 

Downstream Products

• 144632-46-2 6-(2-carboxymethyl)pyrrolidin-1-yl-3,5-dimethyl-5-phenyl-1,2-oxazine N-oxide 
• 144632-57-5 methyl 2-methyl-2-nitro-1-phenyl-3-(1-phenylethyl)hexahydro-1H-pyrrolizine-7a-carboxylate 
• 144632-57-5 methyl 2-methyl-2-nitro-1-phenyl-3-(1-phenylethyl)hexahydro-1H-pyrrolizine-7a-carboxylate 
• 144632-52-0 2-methyl-4-nitro-2,3-diphenylbutyraldehyde 
• 144632-61-1 methyl decahydro-5a-nitro-5-(1-phenylethyl)cyclopentisoindole-9b-carboxylate 
• 144632-59-7 methyl 2-nitro-1,2-diphenyl-3-(1-phenylethyl)hexahydropyrrolizine-7a-carboxylate 
• 144632-49-5 2,3-dimethyl-4-nitro-2-phenylbutanal 
• 144632-44-0 1-(2-carboxymethyl)pyrrolidin-1-yl-2,3-dimethyl-4-nitro-2-phenylcyclobutane 
• 144632-53-1 2-methyl-4-oxo-2-phenylpentanal 
• 144632-47-3 3-(2-carboxymethyl)pyrrolidin-1-yl-4-methyl-4-phenylcyclopent<2,1>oxazine N-oxide 
• 144632-60-0 methyl 5a-nitro-5-(1-phenylethyl)cyclopenthexahydropyrrolizine-8b-carboxylate 
• 144632-43-9 1-(2-carboxymethyl)pyrrolidin-1-yl-2-methyl-4-nitro-2-phenylcyclobutane 
• 144632-48-4 2-methyl-4-nitro-2-phenylbutanal 

Relevant academic research and scientific papers

N-(2-Phenylprop-1-enyl)proline Methyl Ester: Equilibrium between the Enamine and the Aza Methine Ylide Form

The title compound reacted with nitroolefins to give either cyclobutanes or pyrrolizidine derivatives, depending on whether it acted as an enamine or as a 1,3-dipole.