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dc.contributor.advisorLe, Quang Phong
dc.contributor.authorPhan, Tuong Ni
dc.date.accessioned2024-03-20T02:04:16Z
dc.date.available2024-03-20T02:04:16Z
dc.date.issued2020-03
dc.identifier.urihttp://keep.hcmiu.edu.vn:8080/handle/123456789/4899
dc.description.abstractDihydro – 1,3,5 – triazines are heterocyclic aromatic compounds whose derivatives were synthesized from aldehydes and characterized by 1H NMR spectra. This kind of compound and their derivatives have potential antibacterial agents, antimalarials and malignancy – infectious disease. This study was conducted to determine the optimal condition of the process of synthesizing target compounds. The research explored the reaction of substituted benzaldehydes with substituted amidine hydrochloride in the presence of DMSO which induces the forming of 1,2 - dihydro – 1,3,5 – triazine derivatives. The results depicted the good yields of the reaction.en_US
dc.language.isoenen_US
dc.subjectNitrogen heterocyclesen_US
dc.subjectDihydro -1,3,5-triazinesen_US
dc.subjectamidine hydrochloridesen_US
dc.titleOne-Step Synthesis Of Dihydro -1,3,5-Triazines From Aldehyesen_US
dc.typeThesisen_US


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