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1,3-Dipolar cycloaddition reactions of benzo[h]naphthyridinium N-phenacylides

1,3-Dipolare Cycloadditionsreaktionen von Benzo[h]naphthyridinium-N-phenacyliden

  • Organische Chemie Und Biochemie
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Abstract

The 1,3-dipolar cycloaddition reactions of 1,5- and 1,6-benzo[h]naphthyridinium N-phenacylides, formedin situ from the appropriate quaternary bromides in basic medium, with acrylonitrile, ethyl acrylate and dimethyl acetylenedicarboxylate were investigated.

Zusammenfassung

Es wurden die 1,3-dipolaren Cycloadditionsreaktionen von 1,5- und 1,6-Benzo[h]naphthyridinium-N-phenacyliden untersucht, diein situ aus den entsprechenden quaternären Bromiden in Gegenwart von Alkali dargestellt wurden. Als Dipolarophile wurden Acrylnitril, Ethylacrylat und Acetylendicarbonsäuredimethylester eingesetzt.

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Authors and Affiliations

  1. Institute of Chemistry, Pedagogical University, PL-42-201, Częstochowa, Poland

    Barbara Bachowska & Wanda Śliwa

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  1. Barbara Bachowska
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  2. Wanda Śliwa
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Bachowska, B., Śliwa, W. 1,3-Dipolar cycloaddition reactions of benzo[h]naphthyridinium N-phenacylides. Monatsh Chem 115, 1101–1106 (1984). https://doi.org/10.1007/BF00798776

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  • DOI: https://doi.org/10.1007/BF00798776

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