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Diazotization and Nitrosation

Maltz et al. (1971) introduced disodium pentacyano(nitrosyl)ferrate (sodium nitro-prusside, 7.7) as nitrosating reagent. This compound has the advantage that it is effective for nitrosations and diazotizations at pH 9-11. This allows the synthesis of alkyldiazenolates (7.9) without deamination by-products, as well as dediazoniations in neutral or weakly alkaline solutions. [Pg.245]

See other pages where Diazotization and Nitrosation is mentioned: [Pg.420]

See also in sourсe #XX -- [ Pg.65 , Pg.67 ]

See also in sourсe #XX -- [ Pg.399 , Pg.400 ]

See also in sourсe #XX -- [ Pg.399 , Pg.400 ]

See also in sourсe #XX -- [ Pg.399 , Pg.400 ]

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Diazotate

Diazotates

Diazotization

Nitrosates

Nitrosating

Nitrosation