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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2007 Volume 17, Issue 2, Pages 128–129 (Mi mendc3401)

This article is cited 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).

Language: English

DOI: 10.1016/j.mencom.2007.03.026



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