Abstract: New sulfur and nitrogen containing heterocycles with monoterpenic skeleton were prepared starting from the corresponding monoterpenic thiosemicarbazones. Chloroacetic acid or ethyl bromoacetate were used to have 2-substituted thiazolidin-4-ones beside indazole 8 resulting from pulegone thiosemicarbazone rearrangement in both acidic or basic media. The structures of the newly obtained compounds were confirmed by analytical mass and NMR spectra, as well as DFT calculations. All synthesized compounds were tested against fungi (Aspergillus fumigatus), yeast (Candida albicans), gram-negative (Acinetobacter baumannii and Pseudomonas aeruginosa) and gram-positive bacteria.............
Keywords: Thiosemicarbazones, monoterpenic thiazolidin-4-one, Indazole, heterocyclisation, DFT calculation, antibacterial and antifungal activities, MIC.
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