Mendeleev Commun., 2011 Volume 21, Issue 5, Pages 277–279
(Mi mendc2943)
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This article is cited in
10 papers
Unexpected spontaneous ring-contraction rearrangement of trifluoromethylated 1,2-oxazine N-oxides to 1-pyrroline N-oxides
V. Yu. Korotaeva,
A. Yu. Barkova,
P. A. Slepukhinb,
M. I. Kodessb,
V. Ya. Sosnovskikha a Department of Chemistry, Ural Federal University, Ekaterinburg, Russian Federation
b I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation
Abstract:
6-Amino-4-trifluoromethyl-5,6-dihydro-4
H-1,2-oxazine 2-oxides undergo spontaneous rearrangement into 4-amino-2-hydroxy-4-trifluoromethyl-3,4-dihydro-2
H-pyrrole 1-oxides.
Language: English
DOI:
10.1016/j.mencom.2011.09.016
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