Abstract
4-iodo-l-methylpyrazoles react with a nitrating mixture at 55 °C to give the corresponding 4-nitro-I-methylpyrazoles. The qualitative dependence of the nitrodeiodination rate on the structure of the heterocycles and the reaction conditions was considered.
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Translated fromlzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2722–2725, November, 1996.
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Tret'yakov, E.V., Vasitevsky, S.F. Nitrodeiodination of 4-iodo-l-methylpyrazoles. Russ Chem Bull 45, 2581–2584 (1996). https://doi.org/10.1007/BF01431120
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DOI: https://doi.org/10.1007/BF01431120