Abstract
An efficient and versatile synthesis of 3-azolyl-6-(1,2-oxazol-5-yl)-2H-chromene-2-ones using a Knoevenagel reaction and subsequent cleavage with hydroxylamine hydrochloride is described.
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We thank Enamine Ltd for providing the 13C NMR spectra.
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Lozinski, O.A., Shokol, T.V. & Khilya, V.P. 4H,8H-Pyrano[2,3-f]chromene-4,8-diones as versatile precursors for the synthesis of 6-(1,2-oxazol-5-yl)-2H-chromene-2-ones. Monatsh Chem 144, 217–222 (2013). https://doi.org/10.1007/s00706-012-0844-z
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DOI: https://doi.org/10.1007/s00706-012-0844-z