154283-91-7

Upstream product

• 124-40-3 dimethyl amine 
• 154284-02-3 C₁₆H₁₇NO₄ 
• 75391-17-2 3-phenyl-3-(1H-pyrrol-1-yl)propanoic acid 
• 3646-50-2 3-Amino-3-phenylpropionic acid 
• 109-97-7 pyrrole 
• 17431-39-9 (E)-N,N-dimethylcinnamamide 

Downstream Products

• 75391-22-9 3-phenyl-2,3-dihydro-1H-pyrrolizin-1-one 
• 154283-87-1 1-methylimino-3-phenyl-2,3-dihydro-1H-pyrrolizine 
• 154283-97-3 1-oximino-3-phenyl-2,3-dihydro-1H-pyrrolizine 
• 154283-98-4 4-phenyl-1,2,3,4-tetrahydropyrrolo<1,2-a>pyrazin-1-one 
• 154283-88-2 1-cyclopentylimino-3-phenyl-2,3-dihydro-1H-pyrrolizine 

Relevant academic research and scientific papers

Pyrrolate-catalyzed conjugate addition of pyrrole to electron-deficient alkenes

The conjugate addition of pyrrole as a nitrogen nucleophile can be catalyzed by potassium pyrrolate in coordinating solvents or by lithium pyrrolate in the presence of coordinating ligands offering an efficient route to protected β-amino carbonyl compound

An Efficient Synthesis of New Phenylpyrrolizine and Phenylpyrrolopyrazine Derivatives

Synthesis of new 3-phenyl-2,3-dihydro-1H-pyrrolizine derivatives is achieved starting from 3-amino-3-phenylpropionic acid via an iminium salt.The reactivity of this system is studied and the new 4-phenyl-1,2,3,4-tetrahydropyrrolopyrazin-1-one deriv