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New type of spin-labeled aminoenal

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Abstract

Ethynyl-substituted nitronyl nitroxide is involved in the 1,3-dipolar cycloaddition with cyclic nitrones without affecting the nitronyl nitroxide fragment. The reaction of 2,4,4,5,5-pentamethyl-4,5-dihydro-1H-imidazole 3-oxide produces the corresponding 1,2,3,7a-tetrahydroimidazo[1,2-b]isoxazole derivative. The analog of the latter derived from 4,4,5,5-tetramethyl-4,5-dihydro-1H-imidazole 3-oxide is transformed into spin-labeled aminoenal. The solid phase of aminoenal is formed by packing unsymmetrical trimers resulting from the self-assembling of the molecular fragments based on a hydrogen bond network.

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Correspondence to V. I. Ovcharenko.

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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 1975–1979, October, 2007.

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Tretyakov, E.V., Ovcharenko, V.I., Sagdeev, R.Z. et al. New type of spin-labeled aminoenal. Russ Chem Bull 56, 2043–2047 (2007). https://doi.org/10.1007/s11172-007-0319-2

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  • DOI: https://doi.org/10.1007/s11172-007-0319-2

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