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Nitrosohydroxylamine derivatives

Insertion of isocyanides R NC (R = MesC or MesSi), which are isoelectronic to CO, appears to be quite similar (Scheme 10) this step has been used to achieve overall hydrocyanation (see Section 3.9.3.4.3). C—S and C—N bonds may also be generated. SO2 inserts with retention of configuration to yield [Cp2ClZr02SR], while NO leads to A(-nitrosohydroxylamine derivatives [Cp2ClZrj ON(NO)R) ]. Neither of the last two has been exploited synthetically. [Pg.692]

Grignard reagents have reacted with diimide dioxides prepared from nitrosohydroxylamines and with toluenesulfonyl derivatives of nitroso-hydroxylamines to prepare unsymmetrical azoxy compounds, including aliphatic-aromatic types. [Pg.180]

A study33 has been made of the rearrangement of /V-triarylmethylanilines to their p-triarylmethyl derivatives. A-Methyl-A-nitrosoaniline has been observed to undergo a Fischer-Hepp rearrangement when treated with montmorillonite clay,34 and /V-aryl-A-nitrosohydroxylamine ammonium salts (30) have been transformed35 into azoxy... [Pg.480]

Hrabie JA, Keefer LK. Chemistry of the nitric oxide-releasing diazeniumdiolate ( nitrosohydroxylamine ) function group and its oxygen-substituted derivatives. Chemical Reviews 2002, 102, 1135-1154. [Pg.265]

Hexamminenickel(II) iodide, 3 194 Hydrates, nomenclature of, 2 264 Hydrazidicarbamide, 4 26 Hydrazine, 1 90 and derivatives, from hydroxyl-amine-O-sulfonic acid, 5 124 derivatives of, by reduction of A -nitrosohydroxylamine-Ar-sulfonates, 6 121 residues, recovery of, 1 92 Hydrazine dihydrochloride, 1 92 Hydrazine urazolate, formation of, in preparation of urazole, 5 53, 54... [Pg.237]

Odm Processes - The benzophenone sensitised reaction of the N,0-diacyl N-phenylhydroxylamine (189) in hexadecyltrimethylanunonium chloride micelles yields benzoyloxy-migrated products (190) and (191) derived from amidyl-benzoyloxyl radical pairs located at the micellar surface, whereas amidyl-phenyl radical pairs that penetrate more deeply into the micelle are responsible for phenyl-migrated products (192) and (193). Irradiation of ethanolic solutions of N-aryl-N-nitrosohydroxylamine ammonium salts produces azoxy compounds. [Pg.251]

Oxidized nitrogen. Aqueous 80s absorbs NO and forms [803N202] , i.e., A-nitrosohydroxylamine-A-sulfonate, a hyponitrite derivative ... [Pg.421]


See other pages where Nitrosohydroxylamine derivatives is mentioned: [Pg.223]    [Pg.434]    [Pg.3]    [Pg.641]    [Pg.223]    [Pg.434]    [Pg.3]    [Pg.641]    [Pg.212]    [Pg.148]    [Pg.191]    [Pg.432]    [Pg.115]    [Pg.118]    [Pg.191]    [Pg.213]    [Pg.264]    [Pg.1019]    [Pg.761]    [Pg.201]    [Pg.246]   


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