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Synthesis and Antibacterial Activities of 4—Amino—3—(1—aryl—5—methyl—1,2,3—triazol—4—yl)—5—mercapto—1,2,4—triazoles/2—Amino—5—(1—aryl—5—methyl—1,2,3—triazol—4—yl)—1,3,4—
引用本文:ZHANG,Yan WANG,Qin 等.Synthesis and Antibacterial Activities of 4—Amino—3—(1—aryl—5—methyl—1,2,3—triazol—4—yl)—5—mercapto—1,2,4—triazoles/2—Amino—5—(1—aryl—5—methyl—1,2,3—triazol—4—yl)—1,3,4—[J].中国化学,2002,20(2):168-173.
作者姓名:ZHANG,Yan  WANG,Qin
作者单位:[1]DepartmentofChemistry,NationalLaboratoryofAppliedOrganicChemistry,LanzhouUniversity,Lanzhou,Gansu730000,China [2]DepartmentofBiology,LanzhouUniversity,Lanzhou,Gansu730000,China
摘    要:Treatment of 4-amino-3-(1-aryl-5-methyl-1,2,3-triazol-4-yl)-5-mercapto-1,2,4-triazoles/2-amino-5-(1-aryl-5-methyl-1,2,3-triazole-4-yl)-1,3,4-thiadiazoles with benzaldehyde,acetone and ω-bromoacetophenone was tested and compared.The title compounds Schiff bases,amides,imidazolo 2,1-b]-1,3,4-thiadiazoles and 7H-s-triazolo3,4-b]-1,3,4-thiadiazines have been confirmed by elemental analyses,^1H NMR,IR and MS spectra.All the compounds have also been screened for their antibacterial activities against B.subtilis,S.aureus and E.coli.

关 键 词:合成  抗菌活性  4-氨基-3-(1-芳基-5-甲基-1,2,3-三唑-4-基)-1,3,4-噻重氮  衍生物
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