| Makale Türü |
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| Dergi Adı | Chemistry and Biodiversity (Q3) | ||
| Dergi ISSN | 1612-1872 Wos Dergi Scopus Dergi | ||
| Dergi Tarandığı Indeksler | SCI-Expanded | ||
| Makale Dili | Türkçe | Basım Tarihi | 10-2023 |
| Cilt / Sayı / Sayfa | 20 / 11 / – | DOI | 10.1002/cbdv.202301063 |
| Makale Linki | https://doi.org/10.1002/cbdv.202301063 | ||
| UAK Araştırma Alanları |
Atom, Molekül ve Lazer Fiziği
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| Özet |
| Eleven new thiosemicarbazone derivatives (1–11) were designed from nine different biologically and pharmacologically important isothiocyanate derivatives containing functional groups such as fluorine, chlorine, methoxy, methyl, and nitro at various positions of the phenyl ring, in addition to the benzyl unit in the molecular skeletal structure. First, their substituted‐thiosemicarbazide derivatives were synthesized from the treatment of isothiocyanate with hydrazine to synthesize the designed compounds. Through a one‐step easy synthesis and an eco‐friendly process, the designed compounds were synthesized with yields of up to 95 % from the treatment of the thiosemicarbazides with aldehyde derivatives having methoxy and hydroxy groups. The structures of the synthesized molecules were elucidated with elemental analysis and FT–IR, 1H‐NMR, and 13C‐NMR spectroscopic methods. The electronic and … |
| Anahtar Kelimeler |
| DFT | enzyme inhibition | molecular docking | structure characterization | thiosemicarbazones |
| Atıf Sayıları | |
| Web of Science | 12 |
| Scopus | 12 |
| Google Scholar | 12 |
| Dergi Adı | CHEMISTRY & BIODIVERSITY |
| Yayıncı | Wiley-Blackwell |
| Açık Erişim | Hayır |
| ISSN | 1612-1872 |
| E-ISSN | 1612-1880 |
| CiteScore | 3,5 |
| SJR | 0,425 |
| SNIP | 0,700 |