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Fischer-Indol-Synthese

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Zusammenfassung

Indole aus Arylhydrazonen Durch Erhitzen von Arylhydrazonen 1 in Gegenwart eines Katalysators erhält man unter Eliminierung von Ammoniak ein Indol 2. Diese Reaktion ist als Fischer-Indol-Synthese 1–7) bekannt und der →Benzidin-Umlagerung ähnlich.

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© 1994 Springer Fachmedien Wiesbaden

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Laue, T., Plagens, A. (1994). Fischer-Indol-Synthese. In: Namen- und Schlagwort-Reaktionen der Organischen Chemie. Teubner Studienbücher Chemie. Vieweg+Teubner Verlag, Wiesbaden. https://doi.org/10.1007/978-3-322-94015-5_40

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  • DOI: https://doi.org/10.1007/978-3-322-94015-5_40

  • Publisher Name: Vieweg+Teubner Verlag, Wiesbaden

  • Print ISBN: 978-3-519-13526-5

  • Online ISBN: 978-3-322-94015-5

  • eBook Packages: Springer Book Archive

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