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NITROARYL COMPOUNDS

Nitroaryl compounds including amino acid and peptide derivatives (Escher and Schwyzer, 1974), chloramphenicol (Sonenberg et al., 1974 which gave much non-specific labeling), and flunitrazepam (Mohler et al., 1980) have been used to photolabel receptors and they probably react via triplet [Pg.19]

See other runaway reactions See other nitroaryl compounds... [Pg.681]

See Other HALOARYL COMPOUNDS, NITROARYL COMPOUNDS, ORGANIC ACIDS... [Pg.697]

See other metal nitrophenoxides, nitroaryl compounds, oc/ -nitroquinonoid... [Pg.707]

See other gas evolution incidents See other NITROARYL COMPOUNDS... [Pg.741]

See Other NITROARYL COMPOUNDS, PERCHLORATE salts of nitrogenous bases... [Pg.776]

See 4-Chloro-3-nitrotoluene Copper(I) cyanide, Pyridine See other cyano compounds, nitroaryl compounds... [Pg.868]

See THERMAL STABILITY OL REACTION MIXTURES AND SYSTEMS See Other CYANO COMPOUNDS, DIAZONIUM SULFATES, INDUCTION PERIOD INCIDENTS, NITROARYL COMPOUNDS... [Pg.870]

See other deflagration incidents, nitroaryl compounds, organic acids... [Pg.880]

See other pages where NITROARYL COMPOUNDS is mentioned: [Pg.500]    [Pg.681]    [Pg.683]    [Pg.695]    [Pg.696]    [Pg.696]    [Pg.697]    [Pg.702]    [Pg.705]    [Pg.711]    [Pg.711]    [Pg.728]    [Pg.743]    [Pg.762]    [Pg.764]    [Pg.765]    [Pg.862]    [Pg.863]    [Pg.863]    [Pg.863]    [Pg.868]    [Pg.870]    [Pg.873]    [Pg.874]    [Pg.877]    [Pg.877]    [Pg.878]    [Pg.879]    [Pg.879]    [Pg.880]    [Pg.882]   
See also in sourсe #XX -- [ Pg.260 ]

See also in sourсe #XX -- [ Pg.16 , Pg.19 ]



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A-Nitroaryl carbonyl compounds

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