Synthesis of methyl (E)-2' ,4'' -thiazachalcones and their N-alkyl derivatives, photochemistry with theoretical calculations and antimicrobial activities
Experimental and theoretical calculation showed that δ -truxinic type dimer is the most stable isomer.
📌 3 Key Takeaways
🎯
Objective & Hypothesis:A series of 9 new (E) -thiazachalcones (1-3), and their N -alkyl substituted derivatives (4-6), and stereoselective dimerization products (7-9) were synthesized, then tested for antimicrobial activity against all test microorganisms except Pseudomonas aeruginosa.
📊
Key Findings & Data:The new compounds (1-6) without dimerization products (7-9) showed good antimicrobial property against Staphylococcus aureus, Listeria monocitogenes, and Enterococcus faecalis.
💡
Conclusion & Impact:Experimental and theoretical calculation showed that δ -truxinic type dimer is the most stable isomer.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
A series of 9 new (E) -thiazachalcones (1-3), and their N -alkyl substituted derivatives (4-6), and stereoselective dimerization products (7-9) were synthesized, then tested for antimicrobial activity against all test microorganisms except Pseudomonas aeruginosa. The new compounds (1-6) without dimerization products (7-9) showed good antimicrobial property against Staphylococcus aureus, Listeria monocitogenes, and Enterococcus faecalis. The possible dimerization products of compounds (1-3) were calculated theoretically. Experimental and theoretical calculation showed that δ -truxinic type dimer is the most stable isomer.
🔖
Cite This Article
USTA, A., YAYLI, N., KARAOĞLU, A. Ş., YAYLI, N., YAŞAR, A. (2022). Synthesis of methyl (E)-2' ,4'' -thiazachalcones and their N-alkyl derivatives, photochemistry with theoretical calculations and antimicrobial activities. Turkish Journal of Chemistry, Cilt: 33 - Sayı: 5, 621–632. https://ajindex.com/articles/602131