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Mendeleev Communications, 2000, Volume 10, Issue 2, Pages 69–71
DOI: https://doi.org/10.1070/MC2000v010n02ABEH001231
(Mi mendc4387)
 

This article is cited in 3 scientific papers (total in 3 papers)

Formation of cyclic ketene N-hydroxyaminals, 2-acylmethylene-1-hydroxyimidazolidines, in the reaction of 1,2-bishydroxylamines with 1,3-ketoaldehydes

D. G. Mazhukin, A. Ya. Tikhonov, V. A. Reznikov, L. B. Volodarsky

N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation
Full-text PDF (103 kB) Citations (3)
Abstract: The reaction of aliphatic 1,2-bishydroxylamines with 1,3-ketoaldehydes generated in situ in acidic media leads to 2-acylmethylene- 1-hydroxyimidazolidines, a new class of cyclic ketene N-hydroxyaminals.
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Document Type: Article
Language: English


Citation: D. G. Mazhukin, A. Ya. Tikhonov, V. A. Reznikov, L. B. Volodarsky, “Formation of cyclic ketene N-hydroxyaminals, 2-acylmethylene-1-hydroxyimidazolidines, in the reaction of 1,2-bishydroxylamines with 1,3-ketoaldehydes”, Mendeleev Commun., 10:2 (2000), 69–71
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  • This publication is cited in the following 3 articles:
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