Generation and trapping of a 1,2,3-triazolium 1-unsubstituted methanide. A carbon analogue of the azole N-oxide: routes to pyrrolo[1,2-c][1,2,3]triazoles and substituted 1-aminopyrroles

Richard N. Butler; Peter D. McDonald; P. McArdle; D. Cunningham

doi:10.1039/P19940001653

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Generation and trapping of a 1,2,3-triazolium 1-unsubstituted methanide. A carbon analogue of the azole N-oxide: routes to pyrrolo[1,2-c][1,2,3]triazoles and substituted 1-aminopyrroles

Richard N. Butler, Peter D. McDonald, P. McArdle and D. Cunningham

Abstract

Trapping of the first azole N-unsubstituted methanide species, a carbon analogue of the ubiquitous azole N-oxide system is described; new synthetic routes to pyrrolo[1,2-c][1,2,3]triazoles and 1-aminopyrroles have resulted.

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DOI: https://doi.org/10.1039/P19940001653
Article type: Paper

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J. Chem. Soc., Perkin Trans. 1, 1994, 1653-1655

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Generation and trapping of a 1,2,3-triazolium 1-unsubstituted methanide. A carbon analogue of the azole N-oxide: routes to pyrrolo[1,2-c][1,2,3]triazoles and substituted 1-aminopyrroles

R. N. Butler, P. D. McDonald, P. McArdle and D. Cunningham, J. Chem. Soc., Perkin Trans. 1, 1994, 1653 DOI: 10.1039/P19940001653

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Journal of the Chemical Society, Perkin Transactions 1

Generation and trapping of a 1,2,3-triazolium 1-unsubstituted methanide. A carbon analogue of the azole N-oxide: routes to pyrrolo[1,2-c][1,2,3]triazoles and substituted 1-aminopyrroles

Abstract

Article information

Download Citation

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Generation and trapping of a 1,2,3-triazolium 1-unsubstituted methanide. A carbon analogue of the azole N-oxide: routes to pyrrolo[1,2-c][1,2,3]triazoles and substituted 1-aminopyrroles

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