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The Gould-Jacobs Reaction of5-Aminoquinoxaline

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Monatshefte für Chemie / Chemical Monthly Aims and scope Submit manuscript

Summary.

 Reaction of 5-aminoquinoxaline with alkoxymethylene derivatives affords the corresponding quinoxalinoaminoethylenes. These undergo a thermal cyclization to yield angularly annelated 10H-pyrido[2,3-f]quinoxalines. The structures of all products were deduced from their IR, UV, mass, 1H, and 13C NMR spectra.

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Authors and Affiliations

  1.  Department of Organic Chemistry, Faculty of Chemical Technology, Slovak University of Technology, SK-81237 Bratislava, Slovak Republic, , , , , , SK

    Jozef Saloň & Viktor Milata

Authors
  1. Jozef Saloň
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  2. Viktor Milata
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  3. Nadežda Prónayová
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  4. Ján Leško
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Additional information

Received September 24, 1999. Accepted November 18, 1999

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Saloň, J., Milata, V., Prónayová, N. et al. The Gould-Jacobs Reaction of5-Aminoquinoxaline. Monatshefte für Chemie 131, 293–299 (2000). https://doi.org/10.1007/s007060070105

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  • DOI: https://doi.org/10.1007/s007060070105

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