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Mendeleev Communications, 2012, Volume 22, Issue 5, Pages 270–272
DOI: https://doi.org/10.1016/j.mencom.2012.09.015 (Mi mendc2816) 		 
This article is cited in 16 scientific papers (total in 16 papers)

Electrochemical Azolation of N-substituted Pyrroles: A New Case in SNH(An) Reactions

V. L. Sigacheva, V. A. Kokorekin, Yu. A. Strelenko, S. V. Neverov, V. A. Petrosyan

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (279 kB) Citations (16)
DOI: https://doi.org/10.1016/j.mencom.2012.09.015
Abstract: Potentiostatic electrolysis (divided cell, anode compartment) of 1-methyl- and 1-phenylpyrroles in the presence of sodium 4-nitro-pyrazolate and sodium 3-nitropyrazolate in MeCN/MeOH gave the corresponding 2-(azol-1-yl)pyrroles in 20–43% current and substance yields.
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Document Type: Article
Language: English


Citation: V. L. Sigacheva, V. A. Kokorekin, Yu. A. Strelenko, S. V. Neverov, V. A. Petrosyan, “Electrochemical Azolation of N-substituted Pyrroles: A New Case in SNH(An) Reactions”, Mendeleev Commun., 22:5 (2012), 270–272
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  • https://www.mathnet.ru/eng/mendc/v22/i5/p270
    • This publication is cited in the following 16 articles:
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