Makale detayı · 2017 · article
Synthesis and antimicrobial activity of new piperazine-based heterocyclic compounds
Veri kaynağı ayrımı
- YÖKSİSYÖKSİS makale kaydı
- YÖKSİS dergi adıHeterocyclic Communications
- Katalog eşleşmesi (ISSN)Heterocyclic Communications
- OpenAlexOpenAlex zenginleştirmesi (özet, atıf, konular)
Özet
Abstract The hydrazide 5 , that was obtained from 1-(4-fluorophenyl)piperazine ( 1 ), was converted to the corresponding carbothioamides 6a–c by the reaction with alkyl(aryl) isothiocyanates. The synthesis of conazole analogs 10a–f was performed via the intermediary of triazoles 7a–c . The condensation of triazoles 7a–c with several heterocyclic amines in the presence of formaldehyde afforded the corresponding N -aminoalkylated triazoles 11–14 . The effect of different catalysts and solvents on conventional and microwave (MW)-prompted reactions was examined. The synthesized compounds were screened for their antimicrobial activities.
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Yerel katalogda bu makaleye atıf yapan 23 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).
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