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Reactions of Oxepino[2,3-с:4,5-с′:6,7-с″]tri(1,2,5-oxadiazole) with N- and O-nucleophiles

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Abstract

Reactions of oxepino[2,3-c:4,5-c′:6,7-c″]tri(1,2,5-oxadiazole) with hydrazine, aliphatic amines, azide- and methoxide aniones, occurring with the opening of ether cycle and generation of 4″-substituted 3,3′:4′,3″-ter-1,2,5-oxadiazol-4-ols, is a convenient synthetic path to unsymmetrically substituted terfurazanes.

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Authors and Affiliations

  1. Special Design and Technological Bureau “Technolog,”, Sovetsky pr. 33А, St. Petersburg, 192076, Russia

    А. А. Astrat’ev, А. I. Stepanov, V. S. Sannikov & D. V. Dashko

Authors
  1. А. А. Astrat’ev
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  2. А. I. Stepanov
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  3. V. S. Sannikov
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  4. D. V. Dashko
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Corresponding author

Correspondence to А. I. Stepanov.

Additional information

Original Russian Text © А.А. Astrat’ev, А.I. Stepanov, V.S. Sannikov, D.V. Dashko, 2015, published in Zhurnal Organicheskoi Khimii, 2015, Vol. 51, No. 11, pp. 1640–1648.

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Astrat’ev, А.А., Stepanov, А.I., Sannikov, V.S. et al. Reactions of Oxepino[2,3-с:4,5-с′:6,7-с″]tri(1,2,5-oxadiazole) with N- and O-nucleophiles. Russ J Org Chem 51, 1610–1619 (2015). https://doi.org/10.1134/S1070428015110160

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  • DOI: https://doi.org/10.1134/S1070428015110160

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