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Cyclization of N-(2-cyclopent-1-en-1-ylphenyl)benzamides in solution and under mass-spectrometric conditions

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Chemistry of Heterocyclic Compounds Aims and scope

The cyclization has been studied of N-(2-cyclopent-1-en-1-ylphenyl)benzamides into the corresponding 3,1-benzoxazines by the action of gaseous hydrogen chloride, trifluoroacetic acid, or bromine, and also under conditions of electron impact in the gas phase. A scheme is proposed for the fragmentation of the molecular ions of the products obtained.

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References

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Authors and Affiliations

  1. Bashkir State University, 32 Zaki Validi, St., Ufa, 450074, Republic of Bashkortostan, Russia

    S. A. Kazaryants

  2. Institute of Organic Chemistry, Ufa Scientific Center of the Russian Academy of Sciences, 71 Oktyabrya Prospect, Ufa, 450054, Republic of Bashkortostan, Russia

    A. S. Erastov, E. G. Galkin, E. M. Vyrypaev, Sh. M. Salikhov & I. B. Abdrakhmanov

Authors
  1. S. A. Kazaryants
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  2. A. S. Erastov
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  3. E. G. Galkin
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  4. E. M. Vyrypaev
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  5. Sh. M. Salikhov
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  6. I. B. Abdrakhmanov
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Corresponding author

Correspondence to S. A. Kazaryants.

Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 432–440, March, 2011.

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Kazaryants, S.A., Erastov, A.S., Galkin, E.G. et al. Cyclization of N-(2-cyclopent-1-en-1-ylphenyl)benzamides in solution and under mass-spectrometric conditions. Chem Heterocycl Comp 47, 355–362 (2011). https://doi.org/10.1007/s10593-011-0764-6

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  • DOI: https://doi.org/10.1007/s10593-011-0764-6

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