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Acetylenchemie 7. Mitt.: Mechanistische Studien zur Synthese von Pyrano-[3,2-c]chinolin-Alkaloiden aus 4-Hydroxychinolin-2-onen und 3-Chlor-3-methylbut-1-in

Acetylenic chemistry, part 7.: Mechanistic studies on the synthesis of pyrano[3,2-c]quinoline-alkaloids from 4-hydroxyquinoline-2-ones and 3-chlor-3-methylbut-1-yne

  • Organische Chemie Und Biochemie
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Abstract

The pyrano-cyclisation of 4-hydroxy-(1-methyl)-1H-quinoline-2-one with 3-chlor-3-methylbut-1-yne, supposed to proceed via an ether or vinyl intermediate, is studied by alkylating different 4-hydroxyquinolines. The nine derivatives characterized favour the ether-pathway (“Späth type” chromene synthesis).

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Authors and Affiliations

  1. Institut für Pharmazeutische Chemie, Universität Münster, D-4400, Münster, Bundesrepublik Deutschland

    Johannes Reisch, Reza A. Salehi-Artimani, Andreas Bathe & Michael Müller

Authors
  1. Johannes Reisch
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  2. Reza A. Salehi-Artimani
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  3. Andreas Bathe
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  4. Michael Müller
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Reisch, J., Salehi-Artimani, R.A., Bathe, A. et al. Acetylenchemie 7. Mitt.: Mechanistische Studien zur Synthese von Pyrano-[3,2-c]chinolin-Alkaloiden aus 4-Hydroxychinolin-2-onen und 3-Chlor-3-methylbut-1-in. Monatsh Chem 119, 781–791 (1988). https://doi.org/10.1007/BF00809691

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  • DOI: https://doi.org/10.1007/BF00809691

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