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Synthesis of 2,2,6,6-tetramethyl-a-diaminoalkylpiperidin-1-oxyls

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

Conclusions

A convenient method was developed for the production of 2,2,6,6-tetramethylpiperidin-1-oxyls with aminoalkyl substituents at position 4 of the piperidine ring. They can be used in the synthesis of spin labels with various lengths in the linking bridge for the modification of macromolecules.

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Authors and Affiliations

  1. B. P. Konstantinov Leningrad Institute of Nuclear Physics, Academy of Sciences of the USSR, Gatchina

    G. N. Bondarev, T. S. Burzina, G. I. Krasotskaya, A. M. Kachurin & A. R. Kleiner

Authors
  1. G. N. Bondarev
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  2. T. S. Burzina
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  3. G. I. Krasotskaya
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  4. A. M. Kachurin
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  5. A. R. Kleiner
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 8, pp. 1850–1855, August, 1985.

The authors express their gratitude to A. I. Sibilev and Z. V. Obukhov for assisting in the work.

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Bondarev, G.N., Burzina, T.S., Krasotskaya, G.I. et al. Synthesis of 2,2,6,6-tetramethyl-a-diaminoalkylpiperidin-1-oxyls. Russ Chem Bull 34, 1700–1704 (1985). https://doi.org/10.1007/BF00948520

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  • DOI: https://doi.org/10.1007/BF00948520

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