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SYNTHESIS OF STABLE OXAZOLIDINE NITROXYL RADICALS WITH METHOXY GROUPS AT THE ALPHA-CARBON ATOMS TO THE RADICAL SITE Full article

Journal BULLETIN OF THE RUSSIAN ACADEMY OF SCIENCES-DIVISION OF CHEMICAL SCIENCE
ISSN: 1063-5211
Output data Year: 1992, Volume: 41, Number: 4, Pages: 758-764 Pages count : 7 DOI: 10.1007/BF01150905
Tags ALPHA-HYDROXYAMINOALCOHOLS; 3-HYDROXYOXAZOLIDINES; STABLE NITROXYL RADICALS; ALPHA-ARYLNITRONES; LEAD DIOXIDE; OXAZOLIDINES
Authors Bakunova S.M. 1 , Grigorev I.A. 1 , Kirilyuk I.A. 1 , Gatilov Yu .V. 1 , Bagryanskaya I.Yu. 1 , Volodarskii L.B. 1
Affiliations
1 Novosibirsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, Novosibirsk 63009

Abstract: The condensation of alpha-hydroxyaminoalcohols with aldehydes and acetone gave 3-hydroxyoxazolidines and tautomeric N-(2-hydroxyethyl)-alpha-arylnitrones, whose oxidation by PbO2 in methanol leads to stable oxazolidine nitroxyl radicals with methoxy groups at C2 and C4.
Cite: Bakunova S.M. , Grigorev I.A. , Kirilyuk I.A. , Gatilov Y.V. , Bagryanskaya I.Y. , Volodarskii L.B.
SYNTHESIS OF STABLE OXAZOLIDINE NITROXYL RADICALS WITH METHOXY GROUPS AT THE ALPHA-CARBON ATOMS TO THE RADICAL SITE
BULLETIN OF THE RUSSIAN ACADEMY OF SCIENCES-DIVISION OF CHEMICAL SCIENCE. 1992. V.41. N4. P.758-764. DOI: 10.1007/BF01150905 WOS Scopus OpenAlex
Dates:
Published print: Apr 1, 1992
Identifiers:
Web of science: WOS:A1992KB91200011
Scopus: 2-s2.0-34249836621
OpenAlex: W2001862556
Citing:
DB Citing
Web of science 5
Scopus 4
OpenAlex 1
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