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NITRO-, AMINO-, AND RELATED QUINOXALINES

This chapter embraces quinoxalines bearing nitrogenous substituents that are joined to the quinoxaline nucleus through their nitrogen atom. However, isocyano-, isocyanato-, and isothiocyanatoquinoxalines will be found in Chapter 7 to ensure that they are adjacent to quinoxalinecarbonitriles. [Pg.255]

Most nitroquinoxalines have been made as precursors for quinoxalinamines. Moreover, the presence of a powerfully electron-withdrawing nitro group in the molecule will activate leaving groups (such as halogeno) toward all sorts of nucleophilic displacement reactions. [Pg.255]

Nitro-, Amino-, and Related Quinoxalines 6.4.2.1. Noncyclization Reactions... [Pg.300]

See other pages where NITRO-, AMINO-, AND RELATED QUINOXALINES is mentioned: [Pg.255]    [Pg.256]    [Pg.258]    [Pg.260]    [Pg.262]    [Pg.264]    [Pg.266]    [Pg.268]    [Pg.270]    [Pg.272]    [Pg.274]    [Pg.276]    [Pg.278]    [Pg.280]    [Pg.282]    [Pg.284]    [Pg.286]    [Pg.288]    [Pg.290]    [Pg.292]    [Pg.294]    [Pg.296]    [Pg.298]    [Pg.302]    [Pg.304]    [Pg.306]    [Pg.308]    [Pg.310]    [Pg.312]    [Pg.314]    [Pg.255]    [Pg.256]    [Pg.258]    [Pg.260]    [Pg.262]    [Pg.264]    [Pg.266]    [Pg.268]    [Pg.270]    [Pg.272]    [Pg.274]    [Pg.276]    [Pg.278]    [Pg.280]    [Pg.282]    [Pg.284]    [Pg.286]    [Pg.288]    [Pg.290]   


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