2010
DOI: 10.1002/chin.201104145
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ChemInform Abstract: Microwave Assisted Novel Synthesis of Isoxazole and Their Antibacterial Activity.

Abstract: Novel isoxazolylchromenones (V) are synthesized via Baker—Venkataraman transformation of esters (III) and subsequent microwave‐assisted reaction of the obtained propanediones (IV) with hydroxylamine.

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“…From the literature survey, it was found that large numbers of isoxazoline derivatives of pharmacological significance were synthesized by the action of hydroxylamine hydrochloride on chalcones in presence of base [14][15][16][17][18][19] . In present communication we have synthesized isoxazolines from chalcones and hydroxylamine hydrochloride using basic alumina as solid support under microwave and the structures of the compounds were confirmed by 1 H NMR, IR, mass spectra and elemental (C, H, N) analysis.…”
Section: Introductionmentioning
confidence: 99%
“…From the literature survey, it was found that large numbers of isoxazoline derivatives of pharmacological significance were synthesized by the action of hydroxylamine hydrochloride on chalcones in presence of base [14][15][16][17][18][19] . In present communication we have synthesized isoxazolines from chalcones and hydroxylamine hydrochloride using basic alumina as solid support under microwave and the structures of the compounds were confirmed by 1 H NMR, IR, mass spectra and elemental (C, H, N) analysis.…”
Section: Introductionmentioning
confidence: 99%
“…Commonly, isoxazoline derivatives are constructed by 1,3-dipolar cycloaddition of alkenes to nitrile oxides generated in situ by dehydration of nitro compounds or dehydrogenation of oximes. ,,, 3-Acetyl- and 3-benzoyl isoxazolines were synthesized by the reaction of alkenes with acetone or acetophenone in the presence of (NH 4 ) 2 Ce(NO 3 ) 6 or (NH 4 ) 2 Ce(NO 3 ) 5 ·4H 2 O involving the intermediate nitro ketones which were further oxidized to the nitrile oxides. Δ 2 - Isoxazolines are also formed via base-catalyzed or catalyst-free cyclization of α,β-unsaturated ketones with hydroxylamine. ,, Isoxazolinylacetates were synthesized from oximes of β,γ-unsaturated ketones by their palladium-mediated nucleometalation/methoxycarbonylation . The same oximes when subjected to palladium-catalyzed [Pd(dba) 3 /phosphine/NaOBu t ] carboetherification together with arylbromides gave 3-aryl-5-benzyl Δ 2 - isoxazolines …”
mentioning
confidence: 99%