Abstract
Reactions of α-bromoacetylphenoxathiin, α-bromoacetylphenoxathiin 10,10-dioxide, or α-bromoacetylthianthrene with certain p-(arylsulfonyl)thiobenzamides lead to the formation of the corresponding 2,4-disubstituted thiazoles. The new compounds were characterized through elemental analysis and spectral data (IR, 1H NMR, and 13C NMR).
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Loloiu, T., Saramet, I., Loloiu, G. et al. Synthesis of New Thiazoles from α-Halohetaryl Ketones. Chemistry of Heterocyclic Compounds 37, 353–359 (2001). https://doi.org/10.1023/A:1017567302267
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DOI: https://doi.org/10.1023/A:1017567302267