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

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

Journal

Mendeleev Communications
ISSN: 0959-9436

Output data

Year: 2000, Volume: 10, Number: 2, Pages: 69-71 Pages count : 3 DOI: 10.1070/MC2000v010n02ABEH001231

Authors

Mazhukin D.G. ¹ , Tikhonov A.Ya. ¹ , Reznikov V.A. ¹ , Volodarsky L.B. ¹

Affiliations

1	(Scopus) N. N. Vorozhtsov Novosibirsk I., Siberian Branch, Russian Academy of Sciences, 630090 Novosibirsk, Russian Federation

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.

Mazhukin D.G. , Tikhonov A.Y. , Reznikov V.A. , Volodarsky L.B.
Formation of cyclic ketene N-hydroxyaminals, 2-acylmethylene-1-hydroxyimidazolidines, in the reaction of 1,2-bishydroxylamines with 1,3-ketoaldehydes
Mendeleev Communications. 2000. V.10. N2. P.69-71. DOI: 10.1070/MC2000v010n02ABEH001231 WOS Scopus РИНЦ

Published print:

Jan 1, 2000

Web of science	WOS:000086323900015
Scopus	2-s2.0-0040183797
Elibrary	13342626
OpenAlex	W2020044787