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This article is cited in 5 scientific papers (total in 5 papers)
Unexpected formation of 4-hydroxy-6-nitroindoles in the intramolecular cyclization of O-(3-amino-5-nitrophenyl)ketoximes
S. S. Vorob'ev, M. D. Dutov, I. A. Vatsadze, V. V. Kachala, Yu. A. Strelenko, A. A. Sedov, S. A. Shevelev
N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Abstract:
The acid-catalysed cyclization of O-(3-amino-5-nitrophenyl)ketoximes unexpectedly gives, along with 6-amino-4-nitrobenzofurans,
4-hydroxy-6-nitroindoles (in a 1:1 ratio).
Citation:
S. S. Vorob'ev, M. D. Dutov, I. A. Vatsadze, V. V. Kachala, Yu. A. Strelenko, A. A. Sedov, S. A. Shevelev, “Unexpected formation of 4-hydroxy-6-nitroindoles in the intramolecular cyclization of O-(3-amino-5-nitrophenyl)ketoximes”, Mendeleev Commun., 17:2 (2007), 128–129
Linking options:
https://www.mathnet.ru/eng/mendc3401 https://www.mathnet.ru/eng/mendc/v17/i2/p128
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