1240422-91-6

Upstream product

• 13515-97-4 methyl 2-aminopropanoate monohydrochloride 
• 1122-91-4 4-bromo-benzaldehyde 
• 2491-20-5 L-alanine methyl ester hydrochloride 

Downstream Products

• 1169984-02-4 (1R,3S,3aR,6aS)-methyl 3-(4-bromophenyl)-octahydro-1,5-dimethyl-4,6-dioxopyrrolo[3,4-c]pyrrole-1-carboxylate 
• 1279107-56-0 (4R,6S,7R)-7-ethyl 4-methyl 6-(4-bromophenyl)-4-methyl-5-azaspiro[2.4]heptane-4,7-dicarboxylate 
• 1370441-49-8 C₃₇H₃₃BrN₂O₆ 
• 1370441-38-5 C₂₈H₂₈BrFN₂O₆ 
• 1370441-48-7 C₃₄H₃₃BrN₂O₇ 
• 1370441-47-6 C₃₄H₃₃BrN₂O₆ 
• 1370441-40-9 C₃₄H₃₃BrN₂O₇ 
• 1370441-24-9 C₂₈H₂₈Br₂N₂O₆ 

Relevant academic research and scientific papers

Synthesis and Electrochemical Estimation of DNA-Binding Capacity of Novel Ferrocene-Containing Pyrrolidines

The design, synthesis, spectral and electrochemical characterization of a series of novel pyrrolidine derivatives have been described. The synthesis was achieved by 1,3-dipolar cycloaddition of azomethine ylides and ferrocene-substituted chalcones, while

Asymmetric construction of 3-vinylidene-pyrrolidine derivatives containing allene moiety via Ag(i)/TF-BiphamPhos-catalyzed 1,3-dipolar cycloaddition of azomethine ylides with diethyl 2-(3,3-diphenylpropa-1,2-dienylidene) malonate

Catalytic asymmetric 1,3-dipolar cycloaddition of various azomethine ylides with diethyl 2-(3,3-diphenylpropa-1,2-dienylidene)malonate has been developed successfully with good to excellent enantioselectivity for the effcient construction of 3-vinylidene-pyrrolidine derivatives containing a unique allene moiety.

Highly enantioselective 1,3-dipolar cycloaddition of azomethine ylides catalyzed by AgOAc/TF-BiphamPhos

A novel and highly efficient AgOAc/TF-BiphamPhos catalytic system shows excellent reactivity, diastereo-/enantioselectivity and structural scope in asymmetric 1,3-dipolar cycloaddition of azomethine ylides, especially derived from various α-substituted α-amino acids, with N-substituted maleimides and other electron-deficient alkenes.