首页> 外文期刊>Indian Journal of Chemistry, Section B. Organic Including Medicinal >Synthesis of 1,5-benzothiazepines:Part XXX-Synthesis and antimicrobial studies of 10-substituted-6a,7-dihydro-6H-7-(4-fluorophenyl)-6-phenyl [1] benzopyrano [3,4-c] [1,5] benzothiazepines
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Synthesis of 1,5-benzothiazepines:Part XXX-Synthesis and antimicrobial studies of 10-substituted-6a,7-dihydro-6H-7-(4-fluorophenyl)-6-phenyl [1] benzopyrano [3,4-c] [1,5] benzothiazepines

机译:1,5-苯并硫氮杂ze的合成:第XXX部分-10-取代的-6a,7-二氢-6H-7-(4-氟苯基)-6-苯基[1]苯并吡喃[3,4-c]的合成和抗菌研究[1,5]苯并硫氮杂s

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摘要

Flavindogenide,3-(4-fluorobenzylidene)-flavanone has been reacted with six 5-substituted-2-aminobenzenethiols,the substituents being halogens as fluoro,chloro bromo,alkyl as methyl and alkoxyl as methoxyl and ethoxyl,to obtain a series of six new compounds,10-substituted-6a,7-dihydro-6H-7-(4-fluorophenyl)-6-phenyl[1] benzopyrano[3,4-c][1,5]benzo-thiazepines 3a-f.The products are characterized on the basis of microanalytical data for elements and IR,~1H NMR,~(19)F NMR and mass spectral studies.All the synthesized compounds have been evaluated for their antimicrobial activity against the bacteria Escherichia coli and GFC (Alteromonas tetraodonis-a new Gram-negative bacteria family) and fungi,Aspergillus niger,A.flavus and Curvularia lunata.All the compounds showed equal/greater bactericidal activity but for 3d showing lesser activity against E.coli and 3c against GFC.
机译:Flavindogenide,3-(4-氟苄叉基)-flavanone已与六个5-取代的-2-氨基苯硫醇反应,取代基是作为氟的卤素,氯溴,作为甲基的烷基以及作为甲氧基和乙氧基的烷氧基,得到一系列的六个新化合物,10-取代的-6a,7-二氢-6H-7-(4-氟苯基)-6-苯基[1]苯并吡喃并[3,4-c] [1,5]苯并-噻嗪类3a-f。根据元素的微观分析数据和IR,〜1H NMR,〜(19)F NMR和质谱研究对产物进行表征。所有合成的化合物均已评估了其对大肠杆菌和GFC细菌的抗菌活性(Alteromonas tetraodonis -革兰氏阴性菌新家族)和真菌,黑曲霉,黄曲霉和弯孢弯曲菌。所有化合物均显示出相同/更大的杀菌活性,但3d对大肠杆菌的活性较低,而3c对GFC的活性较低。

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