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Synthesis of 3-functionally substituted 4-oximinopiperidin-nitroxyls

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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Conclusions

  1. 1.

    3-Chloro-and 3-bromo-2,2,6,6-tetramethyl-4-oxopiperidin-1-oxyls and their diamagnetic analogs do not react with nucleophilic reagents.

  2. 2.

    3-Functionally substituted 4-oximinopiperidin-nitroxyls were prepared by reaction of 3-chloro-2,2,6, 6-tetramethyl-4-oximinopiperidin-1-oxyl with nucleophilic reagents.

  3. 3.

    An anti-configuration of the oxime group of the α-substituted oxinies synthesized was established.

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Literature cited

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Translated from Izvestiya Akademii Nauk SSR, Seriya Khimicheskaya, No. 7, pp. 1619–1622, July, 1984.

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Krinitskaya, L.A., Volodarskii, L.B. Synthesis of 3-functionally substituted 4-oximinopiperidin-nitroxyls. Russ Chem Bull 33, 1486–1488 (1984). https://doi.org/10.1007/BF00956532

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  • DOI: https://doi.org/10.1007/BF00956532

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