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Syntheses based on α-azidooximes: I. Reduction of α-azidooximes

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Abstract

Convenient procedures were developed for selective and exhaustive reduction of α-azido-oximes that were easily prepared from aliphatic nitro compounds. Nitroalkanes were shown to be convenient precursors of β-functionalized amines (1,2-diamines, iminophosphonates, β azidohydroxyl-amines, α-aminooximes).

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Authors and Affiliations

  1. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, 119991, Russia

    A. Yu. Sukhorukov, A. N. Semakin, A. V. Lesiv, Yu. A. Khomutova & S. L. Ioffe

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  1. A. Yu. Sukhorukov
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  2. A. N. Semakin
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  3. A. V. Lesiv
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  4. Yu. A. Khomutova
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  5. S. L. Ioffe
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Corresponding author

Correspondence to S. L. Ioffe.

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Dedicated to the Full Member of the Russian Academy of Sciences V.A. Tartakovsky on occasion of his 75th birthday

Original Russian Text © A.Yu. Sukhorukov, A.N. Semakin, A.V. Lesiv, Yu.A. Khomutova, S.L. Ioffe, 2007, published in Zhurnal Organicheskoi Khimii, 2007, Vol. 43, No. 8, pp. 1118–1124.

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Sukhorukov, A.Y., Semakin, A.N., Lesiv, A.V. et al. Syntheses based on α-azidooximes: I. Reduction of α-azidooximes. Russ J Org Chem 43, 1106–1113 (2007). https://doi.org/10.1134/S1070428007080027

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  • DOI: https://doi.org/10.1134/S1070428007080027

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