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New type of ring-chain tautomerism. Direct evidence from 1H NMR spectroscopy

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Russian Chemical Bulletin Aims and scope

Abstract

A new type of ring-chain tautomerism consisting in the reversible transformation of 4-(5-)haloalkanecarboxylic acid dialkylamides into dialkyl(tetrahydrofuran-2-ylidene)- and dialkyl(tetrahydropyran-2-ylidene)ammonium halides, respectively, was found and studied by 1H NMR spectroscopy.

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Authors and Affiliations

  1. N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation

    M. V. Zlokazov, A. V. Lozanova & V. V. Veselovsky

Authors
  1. M. V. Zlokazov
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  2. A. V. Lozanova
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  3. V. V. Veselovsky
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Zlokazov, M.V., Lozanova, A.V. & Veselovsky, V.V. New type of ring-chain tautomerism. Direct evidence from 1H NMR spectroscopy. Russian Chemical Bulletin 53, 547–550 (2004). https://doi.org/10.1023/B:RUCB.0000035634.33295.0c

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  • DOI: https://doi.org/10.1023/B:RUCB.0000035634.33295.0c

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