Abstract
5-(1,2,3,4-Tetrahydroxybutyl)-2-methylfuran-3-carbohydrazide (2) was condensed with a variety of ketones to afford carbohydrazide derivatives 3-6. Acetylation of 3-5 afforded the acetyl derivatives 7-9, while periodate oxidation of 3-6 afforded the formyl derivatives 10-13. Acid catalyzed condensation of thiosemicarbazide or o-tolylthiosemicarbazide with the prepared aldehydes 10-12 gave thiosemicarbazone derivatives 14-19. Cyclization of the latter with acetic anhydride afforded 4,5-dihydro- 1,3,4-thiadiazolyl derivatives 20-25. On the other hand, condensation of p-tosylhydrazine with the prepared aldehydes 10-12 afforded p-tosylhydrazone derivatives 26-28. Cyclization of 26-28 with acetic anhydride afforded 1,2,3,4-oxathiadiazole derivatives 29-31 respectively. Moreover, the obtained results regarding to the effect of some of the prepared compounds on tyrosinase enzyme showed that the majority of these compounds having an inhibitory effect; especially compounds 12, 16, 17, and 28. © 2012 by the authors.
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El-Sadek, M. M., Hassan, S. Y., Abdelwahab, H. E., & Yacout, G. A. (2012). Synthesis of new 1,3,4-thiadiazole and 1,2,3,4-oxathiadiazole derivatives from carbohydrate precursors and study of their effect on tyrosinase enzyme. Molecules, 17(7), 8378–8396. https://doi.org/10.3390/molecules17078378
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