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Azyline

Azyline), is formed by the action of nitric oxide on dimethyl-aniline, and by action of paradiazodimethylaniline on the same amine [22]. [Pg.42]

S)-Aziridine-2-carboxylic acid (1), also named azyline (Azy)J4L42] exhibits an electron-withdrawing or quasi-aromatic effect on the nitrogen and is therefore susceptible to an attack by nucleophiles. [41 43] Unprotected aziridine-2-carboxylic acid (1) is very labile, but the [Pg.55]

Trivial names, numbering of substituents in and on the rings are based on azyline, proline, and pipecolic acid. [Pg.55]


See other pages where Azyline is mentioned: [Pg.53]   
See also in sourсe #XX -- [ Pg.42 ]




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