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This article is cited in 13 scientific papers (total in 13 papers)
N-Nitropyrazoles, a new source of nitrogen monoxide
N. B. Grigorieva, V. I. Levinaa, S. A. Shevelevb, I. L. Dalingerb, V. G. Granikc a Centre for Medicinal Chemistry. Sergo Ordzhonikidze All-Russian Research Chemical-Pharmaceutical Institute, Moscow, Russian Federation
b N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
c Russian Research Centre 'Research Institute of Organic Intermediates and Dyes', Moscow, Russian Federation
Abstract:
Electrochemical reduction of N-nitropyrazoles, and chemical reduction by cysteine or potassium ferrocyanide, results in nitrogen monoxide.
Citation:
N. B. Grigoriev, V. I. Levina, S. A. Shevelev, I. L. Dalinger, V. G. Granik, “N-Nitropyrazoles, a new source of nitrogen monoxide”, Mendeleev Commun., 6:1 (1996), 11–12
Linking options:
https://www.mathnet.ru/eng/mendc4889 https://www.mathnet.ru/eng/mendc/v6/i1/p11
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