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Dissociative and Photochemical Mechanisms of Intramolecular Tautomerism

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Molecular Design of Tautomeric Compounds

Part of the book series: Understanding Chemical Reactivity ((UCRE,volume 3))

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Abstract

The tautomeric rearrangements described in the previous Chapters of this book are based on associative mechanisms of nucleophilic substitution. Fitting of a molecular structure to the structure of a transition state or an intermediate of a rearrangement reaction is an effective approach to the design of an intramolecular tautomeric system.

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Authors and Affiliations

  1. Institute of Physical and Organic Chemistry, University of Rostov, Rostov on Don, USSR

    V. I. Minkin, L. P. Olekhnovich & Yu. A. Zhdanov

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  1. V. I. Minkin
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  2. L. P. Olekhnovich
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  3. Yu. A. Zhdanov
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Editors and Affiliations

  1. Institute of Physical and Organic Chemistry, University of Rostov, Rostov on Don, USSR

    V. I. Minkin , L. P. Olekhnovich  & Yu. A. Zhdanov ,  & 

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Minkin, V.I., Olekhnovich, L.P., Zhdanov, Y.A. (1988). Dissociative and Photochemical Mechanisms of Intramolecular Tautomerism. In: Minkin, V.I., Olekhnovich, L.P., Zhdanov, Y.A. (eds) Molecular Design of Tautomeric Compounds. Understanding Chemical Reactivity, vol 3. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-1429-2_6

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  • DOI: https://doi.org/10.1007/978-94-009-1429-2_6

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  • Print ISBN: 978-94-010-7140-6

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