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Current Trends in Organic Synthesis pp 267–274Cite as

Allenes in Novel Palladium-Catalyzed and Acid-Mediated Cyclization Processes

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Abstract

The unique location of two orthogonal carbon carbon double bonds in the aliene moiety makes this functional group suitable for consecutive (tandem) reactions and the rapid build-up of molecular complexity.1 An addition reaction to one double bond usually leads either to an allylic or a vinylic functional group, or to both, which in several cases leads to enhanced reactivity of the molecule for further processes.

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Authors and Affiliations

  1. Laboratory of Organic Chemistry, Institute of Molecular Chemistry, University of Amsterdam, Nieuwe Achtergracht 129, 1018 WS, Amsterdam, The Netherlands

    Henk Hiemstra, Winfred G. Beyersbergen van Henegouwen, Willem F. J. Karstens, Marinus J. Moolenaar & Floris P. J. T. Rutjes

Authors
  1. Henk Hiemstra
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  2. Winfred G. Beyersbergen van Henegouwen
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  3. Willem F. J. Karstens
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  4. Marinus J. Moolenaar
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  5. Floris P. J. T. Rutjes
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Editors and Affiliations

  1. University of Milan, Milan, Italy

    Carlo Scolastico  & Francecso Nicotra  & 

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© 1999 Springer Science+Business Media New York

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Hiemstra, H., van Henegouwen, W.G.B., Karstens, W.F.J., Moolenaar, M.J., Rutjes, F.P.J.T. (1999). Allenes in Novel Palladium-Catalyzed and Acid-Mediated Cyclization Processes. In: Scolastico, C., Nicotra, F. (eds) Current Trends in Organic Synthesis. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-4801-0_33

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  • DOI: https://doi.org/10.1007/978-1-4615-4801-0_33

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4613-7175-5

  • Online ISBN: 978-1-4615-4801-0

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