Reactions of polyfluorinated chalcones with hydroxylamine and subsequent intramolecular cyclization Full article
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Journal of Fluorine Chemistry
ISSN: 1873-3328 , E-ISSN: 0022-1139 |
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| Output data | Year: 2026, Volume: 292, Article number : 110591, Pages count : 8 DOI: 10.1016/j.jfluchem.2026.110591 | ||||||
| Tags | Polyfluorinated chalcones Reactions with hydroxylamine Oximes Dihydroquinolines Benzisoxazole | ||||||
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Abstract:
Polyfluorinated chalcones react with hydroxylamine hydrochloride to form oximes, 3-hydroxylaminooximes, dihydroquinoline and benzisoxazole derivatives, depending on the chalcone structure and the reaction conditions. The last two structure types are formed as a result of intramolecular cyclization by replacing the ortho-fluorine atom in the perfluoro phenyl ring next to the carbonyl group.
Cite:
Gavrilov I.N.
, Orlova N.A.
, Demakov P.A.
, Rybalova T.V.
Reactions of polyfluorinated chalcones with hydroxylamine and subsequent intramolecular cyclization
Journal of Fluorine Chemistry. 2026. V.292. 110591 :1-8. DOI: 10.1016/j.jfluchem.2026.110591
Reactions of polyfluorinated chalcones with hydroxylamine and subsequent intramolecular cyclization
Journal of Fluorine Chemistry. 2026. V.292. 110591 :1-8. DOI: 10.1016/j.jfluchem.2026.110591
Dates:
| Submitted: | May 15, 2026 |
| Accepted: | Jun 15, 2026 |
| Published online: | Jun 23, 2026 |
| Published print: | Jul 1, 2026 |
Identifiers:
No identifiers