Abstract:
The nitro group in 3-substituted 4-nitrofuroxans (4-nitro-1,2,5-oxadiazol 2-oxides) can be replaced by the hydride ion under the action of NaBH4 in EtOH, and this reaction is convenient for the preparation of 3-monosubstituted furoxans.
Document Type:
Article
Language: English
Citation:
A. N. Blinnikov, N. N. Makhova, “Novel synthesis of 3-monosubstituted furoxans”, Mendeleev Commun., 9:1 (1999), 13–15
Linking options:
https://www.mathnet.ru/eng/mendc4505
https://www.mathnet.ru/eng/mendc/v9/i1/p13
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Katie J. Alexander, Matthew McConville, Kathryn R. Williams, Konstantin V. Luzyanin, Ian A. O'Neil, Richard Cosstick, “Chemistry of the 8‐Nitroguanine DNA Lesion: Reactivity, Labelling and Repair”, Chemistry A European J, 24:12 (2018), 3013
Ryosuke Matsubara, Akihiro Ando, Yuta Saeki, Kazuo Eda, Naoki Asada, Tomoaki Tsutsumi, Yong Soon Shin, Masahiko Hayashi, “Synthesis of Furoxans (1,2,5‐oxadiazole 2‐oxides) from Styrenes and Nitrosonium Tetrafluoroborate in Non‐Acidic Media and Mechanistic Study”, Journal of Heterocyclic Chem, 53:4 (2016), 1094
N. N. Makhova, A. S. Kulikov, “Advances in the chemistry of monocyclic amino- and nitrofuroxans”, Russian Chem. Reviews, 82:11 (2013), 1007–1033
G. Nikonov, S. Bobrov, Comprehensive Heterocyclic Chemistry III, 2008, 315
Hugo Cerecetto, Mercedes González, Topics in Heterocyclic Chemistry, 10, Bioactive Heterocycles IV, 2007, 265
Aleksei B. Sheremetev, Nina N. Makhova, Willy Friedrichsen, Advances in Heterocyclic Chemistry, 78, 2001, 65
Alexander N. Blinnikov, Nina N. Makhova, “ChemInform Abstract: Novel Synthesis of 3‐Monosubstituted Furoxans.”, ChemInform, 30:28 (1999)
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