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This article is cited in 2 scientific papers (total in 2 papers)
Intramolecular cyclization of O-(3,5-diaminophenyl)-substituted ketoximes as a route to 6-amino-4-hydroxyindoles
G. V. Kokurkina, M. D. Dutov, S. A. Shevelev, B. I. Ugrak N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Abstract:
O-(3,5-Diaminophenyl)-substituted ketoximes undergo acid-catalysed cyclization to afford 6-amino-4-hydroxyindoles.
Citation:
G. V. Kokurkina, M. D. Dutov, S. A. Shevelev, B. I. Ugrak, “Intramolecular cyclization of O-(3,5-diaminophenyl)-substituted ketoximes as a route to 6-amino-4-hydroxyindoles”, Mendeleev Commun., 21:4 (2011), 196–197
Linking options:
https://www.mathnet.ru/eng/mendc2914 https://www.mathnet.ru/eng/mendc/v21/i4/p196
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