Reduction of alpha,alpha-dialkoxy-substituted nitroxides: the synthesis of alpha-alloxynitrones and acetals of N-hydroxyamides

Reduction of alpha,alpha-dialkoxy-substituted nitroxides: the synthesis of alpha-alloxynitrones and acetals of N-hydroxyamides Full article

Journal

Russian Chemical Bulletin
ISSN: 1066-5285 , E-ISSN: 1573-9171

Output data

Year: 1999, Volume: 48, Number: 11, Pages: 2136-2143 Pages count : 8 DOI: 10.1007/BF02494863

Tags

nitroxides; alpha-alkoxynitrones; alpha-methoxynitrones; 2,5-dihydroimidazoles; 2,5-dihydroimidazole 3-oxides; 2H-imidazole N-oxides; 4H-imidazole N-oxides; 4,5-dihydrooxazole 3-oxides; ring-chain tautomerism

Authors

Bakunova S.M. ¹ , Grigor'ev I.A. ¹ , Kirilyuk I.A. ¹ , Volodarsky L.B. ¹

Affiliations

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

Reduction of stable nitroxides derived from tetrahydrooxazole, tetrahydroimidazole, 2,5-dihydroimidazole, and 2,5-dihydroimidazole 3-oxide containing alkoxy groups in alpha-position to the nitroxyl group affords alpha-alkoxynitrones, acetals of N-hydroxyamides, or their equilibrium mixtures.

Bakunova S.M. , Grigor'ev I.A. , Kirilyuk I.A. , Volodarsky L.B.
Reduction of alpha,alpha-dialkoxy-substituted nitroxides: the synthesis of alpha-alloxynitrones and acetals of N-hydroxyamides
Russian Chemical Bulletin. 1999. V.48. N11. P.2136-2143. DOI: 10.1007/BF02494863 WOS Scopus РИНЦ OpenAlex

Published print:

Nov 1, 1999

Web of science:	WOS:000084420700025
Scopus:	2-s2.0-0033475523
Elibrary:	13331712
OpenAlex:	W2950537769

DB	Citing
Web of science	6
Scopus	7
Elibrary	5
OpenAlex	5