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首页> 外文期刊>Phosphorus, Sulfur, and Silicon and the Related Elements >Syntheses of 1,5-benzothiazepines - Part XXXI: Syntheses and antimicrobial studies of 10-substituted-7(monochlorophenyl/dichlorophenyl)-6H-6a,7-dihydro-6-phenyl[1]benzopyrano[3,4-c]-[1,5]benzothiazepines
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Syntheses of 1,5-benzothiazepines - Part XXXI: Syntheses and antimicrobial studies of 10-substituted-7(monochlorophenyl/dichlorophenyl)-6H-6a,7-dihydro-6-phenyl[1]benzopyrano[3,4-c]-[1,5]benzothiazepines

机译:1,5-苯并硫氮杂s类化合物的合成-第XXXI部分:10-取代的7(一氯苯基/二氯苯基)-6H-6a,7-二氢-6-苯基[1]苯并吡喃[3,4-c]-的合成和抗菌研究[1,5]苯并噻氮平

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摘要

Two flavindogenides, 3-(2-chlorobenzylidene)-flavanone and 3-(2,4-dichlorobenzylidene)-flavanone reacted with six 5-substittited-2-aminobenzenethiols, the substituents being fluoro, chloro, bromo, methyl, methoxyl, and ethoxyl, to give respective 12 new compounds, 10-substititted-7-(2-chlorophenyl/2,4-dichlorophenyl)-6H-6a,7-dihydro-6-phenyl[1]benzopyrano[3,4-c][1,5]benzothiazepines (5a-1) in 60-70% yields. The products were characterized on the basis of microanalytical data for elements and. IR, H-1, and C-13 NMR and mass spectral studies. All the synthesized compounds were evaluated for their antimicrobial activity against the bacteria, Escherichia coli and GFC, and the fungi, Aspergillus niger, Aspergillus flavus, and Curvularia lunata.
机译:两种黄酮,3-(2-氯苄叉基)-黄酮和3-(2,4-二氯苄叉基)-黄酮与六个5-取代的-2-氨基苯硫醇反应,取代基为氟,氯,溴,甲基,甲氧基和乙氧基。 ,分别得到12个新化合物,即10-取代的7-(2-氯苯基/ 2,4-二氯苯基)-6H-6a,7-二氢-6-苯基[1]苯并吡喃并[3,4-c] [1 ,5]苯并硫氮杂ze(5a-1),产率为60-70%。根据元素和元素的微观分析数据对产品进行表征。 IR,H-1和C-13 NMR和质谱研究。评价所有合成的化合物对细菌,大肠杆菌和GFC以及真菌,黑曲霉,黄曲霉和弯孢弯曲菌的抗菌活性。

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