72011-33-7

Upstream product

• 119072-55-8 tert-butylisonitrile 
• 49678-79-7 3t-(4-chloro-phenyl)-2-cyano-1-phthalimido-aziridine-2r-carboxylic acid methyl ester 

Downstream Products

• 136918-14-4 phthalimide 
• 72011-42-8 1-(methoxycarbonyl)-2-aza-1-cyano-3-(p-chlorophenyl)-4-phthalimido-4-(tert-butylamino)buta-1,3-diene 
• 84118-24-1 [(E)-(Z)-2-tert-Butylamino-1-(4-chloro-phenyl)-2-methoxy-vinylimino]-cyano-acetic acid methyl ester 
• 1875-48-5 N-aminophthalamide 
• 84130-26-7 methyl 2-cyano-3-(tert-butylamino)-4-(p-chlorophenyl)but-2-enoate 
• 84118-23-0 [(E)-(E)-2-Amino-2-tert-butylamino-1-(4-chloro-phenyl)-vinylimino]-cyano-acetic acid methyl ester 

Relevant academic research and scientific papers

Cycloadditions of Isocyanides to Azomethine Ylides. Synthesis and Properties of 1-Phthalimidoazetidines

Reactions of isocyanides with 1-phthalimidoaziridines 1,5, and 11 gave 1-phthalimidoazetidines by cycloaddition to the azomethine ylides that are in equilibrium with the aziridines. (tert-Butylimino)azetidines and (tert-octylimino)azetidines rearranged into open-chain azadienes.Reactions of hydrazine hydrate with 1-phthalimidoazetidines did not give the corresponding N-aminoazetidines, but rather their decomposition products, nitrogen and enamino esters.