SYNTHESIS OF STABLE OXAZOLIDINE NITROXYL RADICALS WITH METHOXY GROUPS AT THE ALPHA-CARBON ATOMS TO THE RADICAL SITE Full article
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BULLETIN OF THE RUSSIAN ACADEMY OF SCIENCES-DIVISION OF CHEMICAL SCIENCE
ISSN: 1063-5211 |
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| 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 | ||
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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
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 |