Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/25911
Title: Synthesis of 4-oxo-3a,4,5,6-tetrahydroimidazo[1,5-b]isoxazole-3-carboxylic acid esters
Authors: Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü.
Coşkun, Necdet
Yılmaz, Bilal
7004177880
7006501968
Keywords: Chemistry
Imidazole
Heterocycles
Adducts
Nitrones
1,3-dipolar cycloaddition
Imidazoline 3-oxides
Diastereoselective addition
Regio
Issue Date: May-2004
Publisher: Taylor & Francis
Citation: 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.
Abstract: 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.
URI: https://doi.org/10.1081/SCC-120030749
https://www.tandfonline.com/doi/pdf/10.1081/SCC-120030749
http://hdl.handle.net/11452/25911
ISSN: 0039-7911
Appears in Collections:Web of Science

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