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The periodate oxidation of nitrones
Journal of the Chemical Society C: Organic, 1966The periodate oxidation of some Δ1-pyrroline 1-oxides with two substituents at C-5 but unsubstituted at C-2 leads to a series of 4-nitrosopentanoic acids. Evidence is adduced for the course of the reaction. An N-alkylhydroxyamino-compound is oxidised in chloroform to the nitroso-compound by tetraethylammonium periodate, a potentially useful reagent ...
A. K. Qureshi, B. Sklarz
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Paired Electrosynthesis of a Nitrone
Chemistry Letters, 1997Abstract Dibutyl N-hydroxylamine was oxidized by WO42−/WO52−/ and BR−/Br2 redox mediators at cathode and anode, respectively. The corresponding nitrone, N-butylidenebutylamine N-oxide, was prepared at the both electrodes in divided and undivided cells. The paired electrosynthesis of the nitrone could be realized with current efficiencies
Tsutomu Nonaka, Wei Li
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Methylene nitrones, a new type of nitrone
Chemical Communications (London), 1968J. E. Baldwin, A. K. Qureshi, B. Sklarz
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ChemInform Abstract: NITRONES IN PHARMACEUTICAL CHEMISTRY [PDF]
Chemischer Informationsdienst, 1978 openaire +3 more sources
Nitrones. 6. .alpha.-(5-Nitroimidazol-2-yl)-N-substituted nitrones
Journal of Medicinal Chemistry, 1973C. M. Lutz +4 more
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Mass spectra of nitrones. Electron impact mass spectra of fluorenone nitrones
Journal of Chemical & Engineering Data, 1981R. M. Srivastava +3 more
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