Reaction of Z isomers of alkylaromatic 1,2-hydroxylamino oximes with 1,2-diketones |
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Authors: | S A Amitina I A Grigor’ev A Ya Tikhonov |
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Institution: | (1) N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 9 prosp. Akad. Lavrent’eva, 630090 Novosibirsk, Russian Federation |
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Abstract: | The reactions of Z isomers of alkylaromatic 1,2-hydroxylamino oximes containing the hydroxylamino group at the primary or secondary carbon atom
with diacetyl afford 6-acetyl-5,6-dihydro-4H-1,2,5-oxadiazines. The reactions of these compounds with alkylaromatic 1,2-diketones produce N-substituted α-aroylnitrones or 6-aroyl-5,6-dihydro-4H-1,2,5-oxadiazines or, alternatively, their tautomeric mixtures.
Dedicated to the memory of Academician V. A. Koptyug on the occasion of the 75th anniversary of his birth.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 6, pp. 1008–1013, June, 2006. |
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Keywords: | hydroxylamino oximes nitrones 1 2 5-oxadiazines 1 2-diketones tautomerism |
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