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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 328 (1986), S. 597-602 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Spin Trapping. III. Studies of Radical Reactions of a Bicyclic 1-Hydroxy-3-imidazoline-3-oxideRadical addition reactions to the nitrono group and the oxidation of the 8-hydroxy-1,4,5,7-tetramethyl-6,8-diazabicyclo[3.2.1]oct-6-en-6-oxide 2b were investigated by e.s.r.-spectroscopy. Oxidation of 2b by Ag2O, PbO2, hydrogenperoxide, tert.-butoxy and benzoyloxy radicals, respectively, yields a bicyclic nitroxide with typical a(N)-value (1,9 mT). Testing a wide range of carbon-centered radicals we did not find, however, any spin adducts in contrast to the literature. Only H-atoms are found to add to the nitrone function of 2b giving a bicyclic nitroxide 4b (R′ = H) with a(N)-value of 1,4 mT, a(Hax) = 2,4 mT. The relationship between a ring-chain tautomerism of 2 as previously described and the formation of radicals has been demonstrated by radical reactions of derivatives of ring opened isomers 5b.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 328 (1986), S. 589-596 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ring-Chain Tautomerism and Reactions of a Bicyclic 1-Hydroxy-3-imidazoline-3-oxideThe reaction of 8-hydroxy-1, 4, 5, 7-tetramethyl-6,8-diaza-bicyclo[3.2.1]-oct-6-en-6-oxide (1), a 2,5-bridged bicyclic 1-hydroxy-3-imidazoline-3-oxide, with NaBH4, dimethyl acetylene dicarboxylate and methylmagnesiumiodide, respectively, yields derivatives of the ring opened isomer 2. Whilst on reaction with phenylisocyanate the bicyclic structure 1 is preserved and the urethane 3 is formed. The ring-chain tautomerism of 1 is important for the application of 1 as a spin trap or radical scavenger.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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