New unsymmetrically substituted triazacyclohexanes: Synthesis, characterisation, antimicrobial properties and DFT study
dc.contributor.author | Amel Messai | |
dc.date.accessioned | 2024-02-18T17:17:04Z | |
dc.date.available | 2024-02-18T17:17:04Z | |
dc.date.issued | 2016-09-21 | |
dc.description.abstract | New five unsymmetrically substituted 1,3,5-triazacyclohexanes compounds, carrying aliphatic as well as aromatic substituent, were synthesized and structural analyses were performed by FTIR, 1H NMR and single crystal X-ray techniques. Experimental research was complemented by quantum mechanical calculations. The present triazacyclohexane rings adopt a chair conformation by both R1 substituents in axial positions and R2 group in an equatorial form. Further, all compounds were screened for their antibacterial and anti-fungal properties. By revealing further insight into triazacyclohexanes systems, the data theoretically predicted and experimentally obtained in current research may be helpful guide for the medicinal chemists. | |
dc.identifier.uri | http://dspace.univ-khenchela.dz:4000/handle/123456789/1497 | |
dc.language.iso | en | |
dc.title | New unsymmetrically substituted triazacyclohexanes: Synthesis, characterisation, antimicrobial properties and DFT study | |
dc.type | Article |
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