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Selective reduction of 6-substituted 1,5-dinitro-3-azabicyclo[3.3.1]non-6-enes

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Abstract

Reduction of 6-substituted 1,5-dinitro-3-azabicyclo[3.3.1]non-6-enes gives either saturated 1,5-diamino-3-azabicyclo[3.3.1]nonane or unsaturated 1,5-diamino-3-azabicyclo[3.3.1]non-6-enes, depending on the conditions and nature of substituent in the substrate.

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Authors and Affiliations

  1. Tolstoy Tula State Pedagogical University, pr. Lenina 125, Tula, 300026, Russia

    I. E. Yakunina, A. N. Shchukin, I. V. Shakhkel’dyan & Yu. M. Atroshchenko

  2. Asineks Ltd., Moscow, Russia

    M. V. Kopyshev

  3. Research Institute of Chemical Diversity, Khimki, Moscow oblast, Russia

    A. N. Shumskii

  4. Nesmeyanov Institute of Organometallic Compounds, Russian Academy of Sciences, ul. Vavilova 28, Moscow, 119991, Russia

    A. A. Yakovenko & K. A. Lysenko

Authors
  1. I. E. Yakunina
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  2. A. N. Shchukin
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  3. M. V. Kopyshev
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  4. I. V. Shakhkel’dyan
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  5. A. N. Shumskii
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  6. A. A. Yakovenko
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  7. K. A. Lysenko
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  8. Yu. M. Atroshchenko
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Corresponding author

Correspondence to I. E. Yakunina.

Additional information

Original Russian Text © I.E. Yakunina, A.N. Shchukin, M.V. Kopyshev, I.V. Shakhkel’dyan, A.N. Shumskii, A.A. Yakovenko, K.A. Lysenko, Yu.M. Atroshchenko, 2011, published in Zhurnal Organicheskoi Khimii, 2011, Vol. 47, No. 6, pp. 862–864.

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Yakunina, I.E., Shchukin, A.N., Kopyshev, M.V. et al. Selective reduction of 6-substituted 1,5-dinitro-3-azabicyclo[3.3.1]non-6-enes. Russ J Org Chem 47, 877–880 (2011). https://doi.org/10.1134/S1070428011060078

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  • DOI: https://doi.org/10.1134/S1070428011060078

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