New N-nitrosoamines. 2. Transformations of tetrahydro-1,3-oxazines into nitrates of N-nitrosoamino alcohols |
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Authors: | Korepin A G Galkin P V Perepelkina E K Glushakova N M Lodygina V P Eremenko I L Nefedov S E Eremenko L T |
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Institution: | (1) Institute of Problems of Chemical Physics, Russian Academy of Sciences, 142432 Chernogolovka, Moscow Region, Russian Federation;(2) N. S. Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences, 31 Leninsky prosp., 119991 Moscow, Russian Federation |
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Abstract: | The reactions of HNO3 with tetrahydro-1,3-oxazines 1a—c produced by aminomethylation of diketopiperazine, isatin, and succinimide, respectively, afforded nitrates of amino alcohols RCH2NH2(CH2)3ONO2]+NO3
– (4a—c) whose subsequent N-nitrosation (NaNO2, AcOH) gave nitrates of N-nitrosoamino alcohols RCH2N(NO)(CH2)3ONO2 (5a—c). The structures of compound 5b,c were established by X-ray diffraction analysis. |
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Keywords: | heterocyclic -carbonyl-containing NH-acids" target="_blank">gif" alt="agr" align="BASELINE" BORDER="0">-carbonyl-containing NH-acids amides tetrahydro-1 3-oxazines destructive nitration N-nitrosation nitrates of amino alcohols and N-nitrosoamino alcohols X-ray diffraction analysis |
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