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Conformation of 2,5-substituted 1,3,2-dioxaborinanes studied by NMR

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The conformation of a series of 2,5-substituted 1,3,2-dioxaborinanes is studied by PMR. The preferred conformation for the majority of compounds has an equatorial group on atom C(5). The 5-nitroderivative exists in the conformation with an axial nitro group.

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Authors and Affiliations

  1. A. V. Bogat-skii Physical Chemistry Institute, Academy of Sciences of the Ukrainian SSR, 270080, Odessa

    V. V. Kuznetsov, K. S. Zakharov, I. V. Petrovskii & A. I. Gren'

Authors
  1. V. V. Kuznetsov
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  2. K. S. Zakharov
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  3. I. V. Petrovskii
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  4. A. I. Gren'
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1107–1109, August, 1990.

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Kuznetsov, V.V., Zakharov, K.S., Petrovskii, I.V. et al. Conformation of 2,5-substituted 1,3,2-dioxaborinanes studied by NMR. Chem Heterocycl Compd 26, 927–929 (1990). https://doi.org/10.1007/BF00480872

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  • DOI: https://doi.org/10.1007/BF00480872

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