Abstract
N-Substituted tetrazole was attempted to formylate which led to the formation of a novel triazene by opening of tetrazole ring via unusual Vilsmeir-Haack reaction. The formed product was proved by spectral analyses and X-Ray diffraction studies.
Keywords: Sydnone, triazole, terazole, formylation, iminium cation, Vilsmeir-Haack reaction.
Graphical Abstract
Letters in Organic Chemistry
Title:Ring Opening of Tetrazole via Unusual Vilsmeir-Haack Reaction Forming Novel Triazenes
Volume: 12 Issue: 2
Author(s): Atukuri Dorababu, Ravindra R. Kamble, H. C. Devarajegowda and Gangadhar Y. Meti
Affiliation:
Keywords: Sydnone, triazole, terazole, formylation, iminium cation, Vilsmeir-Haack reaction.
Abstract: N-Substituted tetrazole was attempted to formylate which led to the formation of a novel triazene by opening of tetrazole ring via unusual Vilsmeir-Haack reaction. The formed product was proved by spectral analyses and X-Ray diffraction studies.
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Cite this article as:
Dorababu Atukuri, R. Kamble Ravindra, Devarajegowda H. C. and Y. Meti Gangadhar, Ring Opening of Tetrazole via Unusual Vilsmeir-Haack Reaction Forming Novel Triazenes, Letters in Organic Chemistry 2015; 12 (2) . https://dx.doi.org/10.2174/157017861202150213102528
DOI https://dx.doi.org/10.2174/157017861202150213102528 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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