67628-19-7

Upstream product

• 15028-40-7 DL-2-phenylglycine methyl ester hydrochloride 
• 555-16-8 4-nitrobenzaldehdye 
• 100-52-7 benzaldehyde 
• 6591-61-3 (S)-Phenylglycine methyl ester 
• 24461-61-8 phenylglycine methyl ester 
• 67627-99-0 N-benzyliden-α-phenyl-glycine methyl ester 

Downstream Products

• 89330-89-2 trimethyl 2-phenyl-5-(4'-nitrophenyl)-3-pyrroline-2,3,4-tricarboxylate 
• 89330-92-7 trimethyl 5-(4'-nitrophenyl)pyrrole-2,3,4-tricarboxylate 
• 28220-76-0 dimethyl 5-(4'-nitrophenyl)-2-phenyl-1H-pyrrole-3,4-dicarboxylate 
• 1423136-60-0 methyl 4-benzoyl-5-(4-nitrophenyl)-2-phenyl-2,5-dihydro-1H-pyrrole-2-carboxylate 
• 75516-79-9 trimethyl t-5-(4-nitrophenyl)-2-phenylpyrrolidine-r-2,c-3,t-4-tricarboxylate 
• 75516-79-9 trimethyl c-5-(4-nitrophenyl)-2-phenylpyrrolidine-r-2,c-3,t-4-tricarboxylate 
• 75516-98-2 (2R,3R)-5-(4-Nitro-phenyl)-2-phenyl-pyrrolidine-2,3-dicarboxylic acid dimethyl ester 
• 75516-79-9 trimethyl c-5-(4-nitrophenyl)-2-phenylpyrrolodine-r-2,c-3,c-4-tricarboxylate 
• 75516-79-9 trimethyl t-5-(4-nitrophenyl)-2-phenylpyrrolodine-r-2,t-3,t-4-tricarboxylate 
• 75516-79-9 (2R,3R,4S,5R)-5-(4-Nitro-phenyl)-2-phenyl-pyrrolidine-2,3,4-tricarboxylic acid trimethyl ester 
• 75516-79-9 (2S,3R,4S,5R)-5-(4-Nitro-phenyl)-2-phenyl-pyrrolidine-2,3,4-tricarboxylic acid trimethyl ester 
• 117316-23-1 C₁₆H₁₃⁽²⁾HN₂O₄ 
• 82461-28-7 methyl c-4-(4-nitrophenyl)-2,7-diphenyl-6,8-dioxo-3,7-diazabicyclo<3.3.0>octane-r-2-carboxylate 
• 113370-55-1 methyl c-4-(4-nitrophenyl)-6,8-dioxo-2-phenyl-7-oxa-3-azabicyclo<3.3.0>octane-r-2-carboxylate 

Relevant academic research and scientific papers

Umpolung of Imines Enables Catalytic Asymmetric Regio-reversed [3+2] Cycloadditions of Iminoesters with Nitroolefins

A copper-catalyzed regio-reversed asymmetric [3+2] cycloaddition of iminoesters with nitroolefins is disclosed for the first time. This method enables the facile synthesis of polysubstituted chiral pyrrolidines bearing at least one chiral quaternary cente

Catalytic chemoselective [3+3] cycloadditions of azomethine ylides with quinone monoimides leading to the construction of a dihydrobenzoxazine scaffold

A chemoselective [3+3] cycloaddition of in situ generated azomethine ylides with quinone monoimides has been established, which efficiently led to the construction of dihydrobenzoxazine frameworks with biological relevance, with excellent chemoselectiviti

Asymmetric organocatalytic formal double-arylation of azomethines for the synthesis of highly enantiomerically enriched isoindolines

Isoindoline derivatives with high enantiomeric purity (up to 98% ee) have been accessed by formal double arylation of azomethines.

X=Y-ZH Systems as Potential 1,3-Dipoles. Part 1. Background and Scope

X=Y-ZH Systems are considered in general terms and divided into four classes according to the number of constituent atoms that possess lone-pair electrons.Those systems in which the central Y atom possesses a lone pair are shown to be capable of participa