Abstract
2-Aryl-4-methyl-5-acetylthiazoles, which were prepared from arylthioamides and chloroacetylacetone, were treated with 6-substituted-3-formylchromones or arylaldehydes to give a series of eighteen new thiazolylchalcones in good yields. The structures of all the synthesized compounds were characterized by 1H NMR, 13C NMR, and ES-MS spectrometry. Additionally, the crystal structures of two of these chalcones were determined by X-ray diffraction analysis. © 2012 HeteroCorporation.
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CITATION STYLE
Tazoo, D., Oniga, O., Bohle, D. S., Chua, Z., & Dongo, E. (2012). General two-step preparation of chalcones containing thiazole. Journal of Heterocyclic Chemistry, 49(4), 768–773. https://doi.org/10.1002/jhet.853
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