Über einige Ringöffnungsreaktionen von Tetrazolo(1,5-b)pyridinen

Authors

  • B. Stanovnik Institut für organische Chemie der Universität Ljubljana, 6 Murnikova, 61000 Ljubljana (Jugoslawien)
  • M. Tišler Institut für organische Chemie der Universität Ljubljana, 6 Murnikova, 61000 Ljubljana (Jugoslawien)

DOI:

https://doi.org/10.2533/chimia.1971.272

Abstract

The six-membered ring of tetrazolo (1,5-b)pyridines is cleaved under the influence of bases. The monocyclic products were isolated in the form of their sodium salts and their structure was determined by means of NMR spectroscopy. Furthermore, it has been shown that certain tetrazolo(1,5-b)-pyridines are transformed at elevated temperatures and in the presence of dimethylsulfoxide into the corresponding pyrido- sulfoximines via pyrido (2,3-c)furoxanes.

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Published

1971-08-31

Issue

Vol. 25 No. 8 (1971): Forschung/Research

Section

Kurze Mitteilungen

License

Copyright (c) 1971 B. Stanovnik

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.

How to Cite

[1]
B. Stanovnik, M. Tišler, Chimia 1971, 25, 272, DOI: 10.2533/chimia.1971.272.