Reaction of Z isomers of alkylaromatic 1,2-hydroxylamino oximes with 1,2-diketones Full article
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Russian Chemical Bulletin
ISSN: 1066-5285 , E-ISSN: 1573-9171 |
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| Output data | Year: 2006, Volume: 55, Number: 6, Pages: 1046-1051 Pages count : DOI: 10.1007/s11172-006-0374-0 | ||
| Tags | hydroxylamino oximes; nitrones; 1,2,5-oxadiazines; 1,2-diketones; tautomerism | ||
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Abstract:
The reactions of Z isomers of alkylaromatic 1,2-hydroxylamino oximes containing the hydroxylamino group at the primary or secondary carbon atom with diacetyl afford 6-acetyl5,6-dihydro-4H-1,2,5-oxadiazines. The reactions of these compounds with alkylaromatic 1,2-diketones produce N-substituted alpha-aroylnitrones or 6-aroy1-5,6-dihydro-4H-1,2,5-oxadiazines or, alternatively, their tautomeric mixtures.
Cite:
Amitina S.A.
, Grigor'ev L.A.
, Tikhonov A.Y.
Reaction of Z isomers of alkylaromatic 1,2-hydroxylamino oximes with 1,2-diketones
Russian Chemical Bulletin. 2006. V.55. N6. P.1046-1051. DOI: 10.1007/s11172-006-0374-0 WOS Scopus РИНЦ OpenAlex
Reaction of Z isomers of alkylaromatic 1,2-hydroxylamino oximes with 1,2-diketones
Russian Chemical Bulletin. 2006. V.55. N6. P.1046-1051. DOI: 10.1007/s11172-006-0374-0 WOS Scopus РИНЦ OpenAlex
Dates:
| Published print: | Jun 1, 2006 |
Identifiers:
| Web of science: | WOS:000242652000016 |
| Scopus: | 2-s2.0-33750716866 |
| Elibrary: | 13508810 |
| OpenAlex: | W1972035782 |