New unsymmetrically substituted triazacyclohexanes: Synthesis, characterisation, antimicrobial properties and DFT study

dc.contributor.authorAmel Messai
dc.date.accessioned2024-02-18T17:17:04Z
dc.date.available2024-02-18T17:17:04Z
dc.date.issued2016-09-21
dc.description.abstractNew 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.urihttp://dspace.univ-khenchela.dz:4000/handle/123456789/1497
dc.language.isoen
dc.titleNew unsymmetrically substituted triazacyclohexanes: Synthesis, characterisation, antimicrobial properties and DFT study
dc.typeArticle
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