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Synthesis of 4-oxo-3a,4,5,6-tetrahydroimidazo[1,5-b]isoxazole-3-carboxylic acid esters

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Coşkun, Necdet
Yılmaz, Bilal

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Taylor & Francis

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Özet

3-Imidazoline 3-oxides react regioselectively with 3-phenylpropanoic acid alkyl esters to give the corresponding 2-phenyl-3a,4,5,6-tetrahydroimidazol 1,5-b]isoxazole-3-carboxylic acid alkyl esters. This adducts convert to imidazole and the corresponding. alkyl 3-oxo-3-phenylpropanoic acid esters when treated with alkoxides or heated under vacuum. Attempts to oxidise the carbon-carbon double bond using KMnO4-FeSO4 led to the formation of heretofore unknown 4-oxo-3a,4,5,6-tetrahydroimidazo[1,5-b]isoxazoles.

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Chemistry, Imidazole, Heterocycles, Adducts, Nitrones, 1,3-dipolar cycloaddition, Imidazoline 3-oxides, Diastereoselective addition, Regio

Alıntı

Coşkun, N. ve Yılmaz, B. (2004). “Synthesis of 4-oxo-3a,4,5,6-tetrahydroimidazo[1,5-b]isoxazole-3-carboxylic acid esters”. Synthetic Communications, 34(9), 1617-1623.

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