Acylation of 1-hydroxyamino-2-hydroxyiminoethanes with α-halo acid chlorides and the preparation of 1-hydroxy-2-oxotetrahydropyrazine 4-oxides

Acylation of 1-hydroxyamino-2-hydroxyiminoethanes with α-halo acid chlorides and the preparation of 1-hydroxy-2-oxotetrahydropyrazine 4-oxides Full article

Journal

Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353

Output data

Year: 1984, Volume: 20, Number: 1, Pages: 97-102 Pages count : DOI: 10.1007/BF00505860

Authors

Tikhonov A. Ya. , Volodarskii L. B. , Belova N. V.

Affiliations

1	(Scopus) Novosibirsk Institute of Organic Chemistry, Novosibirsk, Russian Federation

The acylation of 1-hydroxyamino-2-hydroxyiminoethanes with α-halo acid chlorides has given the products of N- and O-acylation at the hydroxyamino group. The action of bases on the products of N-acylation - N-(2-hydroxyiminoalkyl)-2-halohydroxamic acids - has given, depending on the conditions, 1-hydroxy-2-oxo-1,2,3,6- or -1,2,5,6-tetrahydropyrazine 4-oxides and 1,2-oxazetidin-3-ones. © 1984 Plenum Publishing Corporation.

Tikhonov A.Y. , Volodarskii L.B. , Belova N.V.
Acylation of 1-hydroxyamino-2-hydroxyiminoethanes with α-halo acid chlorides and the preparation of 1-hydroxy-2-oxotetrahydropyrazine 4-oxides
Chemistry of Heterocyclic Compounds. 1984. V.20. N1. P.97-102. DOI: 10.1007/BF00505860 Scopus РИНЦ

Scopus	2-s2.0-34250132238
Elibrary	30918860
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