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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
Fulltext:
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Steklov Math. Inst. of RAS
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