83466-70-0

Upstream product

• 941-69-5 N-phenyl-maleimide 
• 39533-32-9 methyl 2-isocyano-2-phenylacetate 
• 24461-61-8 phenylglycine methyl ester 
• 111680-71-8 2-(dimethylamino)-4-oxo-4H-pyrido<1,2-a>pyrimidine-3-carbaldehyde 
• 63856-31-5 Methylsulfanylmethyleneamino-phenyl-acetic acid methyl ester 

Relevant academic research and scientific papers

Asymmetric formal [3+2] cycloaddition reaction of α-aryl isocyanoesters with N-aryl maleimides by bifunctional cinchona alkaloids-based squaramide/AgSbF6 cooperative catalysis

It is better to be cooperative: A highly diastereo- and enantioselective asymmetric [3+2] cycloaddition reaction of α-aryl isocyanoacetates with N-aryl maleimides through cooperative catalysis of cinchona alkaloid-derived squaramide/AgSbF6 was

Generation of functionalized azomethine ylides and their application to stereoselective heterocycle synthesis: an equivalent process of C-unsubstituted nitrile ylide cycloaddition reaction

The synthetic process equivalent to C-unsubstituted (CH) nitrile ylides cycloaddition reaction is achieved via cycloaddition of NH-azomethine ylide and the following fission reaction of the cycloadducts under acidic conditions. Cycloaddition of NH-azometh

X=Y-ZH SYSTEMS AS POTENTIAL 1,3-DIPOLES. CYCLOADDITIONS OF THIOIMINOETHERS AND THIOIMINOCARBONATES

Thioiminoethers and thioiminocarbonates of α-amino acid esters undergo acetic acid catalysed cycloaddition reactions with N-phenylmaleimide via their 1,3-dipolar tautomers.