83466-75-5

Upstream product

• 941-69-5 N-phenyl-maleimide 
• 15028-44-1 DL-phenylalanine methyl ester 
• 111680-71-8 2-(dimethylamino)-4-oxo-4H-pyrido<1,2-a>pyrimidine-3-carbaldehyde 
• 83466-71-1 2-Methylsulfanylmethyleneamino-3-phenyl-propionic acid methyl ester 

Relevant academic research and scientific papers

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.