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Fragmentation of substituted 2-sila-1,3-dioxacycloalkanes under electron impact

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The mass spectrometric dissociation of 2-sila-1,3-dioxacycloalkanes takes place mainly with loss of the substituent from position 2 of the heterocycle. The fragment formed here eliminates the molecular of carbonyl compounds or alkenes.

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Authors and Affiliations

  1. Ufa Petroleum Institute, 450062, Ufa

    R. S. Musavirov, I. A. Kondrat'eva, A. G. Kitov, E. P. Nedogrei, A. A. Kuz'michev, E. A. Kantor, S. S. Zlot-skii & D. L. Rakhmankulov

Authors
  1. R. S. Musavirov
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  2. I. A. Kondrat'eva
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  3. A. G. Kitov
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  4. E. P. Nedogrei
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  5. A. A. Kuz'michev
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  6. E. A. Kantor
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  7. S. S. Zlot-skii
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  8. D. L. Rakhmankulov
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 272–275, February, 1986.

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Musavirov, R.S., Kondrat'eva, I.A., Kitov, A.G. et al. Fragmentation of substituted 2-sila-1,3-dioxacycloalkanes under electron impact. Chem Heterocycl Compd 22, 221–224 (1986). https://doi.org/10.1007/BF00519949

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  • DOI: https://doi.org/10.1007/BF00519949

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