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A Study of Antibacterial Activity of Some Novel 8-Methoxy-4-methyl-quinoline Derivatives
Singh, Sheoraj,Kumar, Vikas,Kumar, Ashok,Sharma, Shalabh,Dua, Piyush Korean Chemical Society 2010 Bulletin of the Korean Chemical Society Vol.31 No.12
In the present study, some quinoline derivatives have been synthesized like 8-methoxy-4-methyl-2-amino-(3'-chloro-2'-oxo-4'-substituted aryl-1'-azetidinyl)quinolines 8-12 and 8-methoxy-4-methyl-2-amino-(2'-substituted aryl-4'-oxo-1',3'-thiazolidin-3'-yl) quinolines 13-17 from 8-methoxy-4-methyl-2-(substituted arylidenyliminoamino)-quinolines 3-7. The structural assignments of these compounds were based on spectral (IR, $^1H$-NMR, Mass) and elemental (C, H, N) analysis. Further, these compounds were evaluated for antibacterial activity against various bacterial strains. Three compounds 10, 11 and 16 were found to exhibit potent antibacterial activity as compared to the standard drug amphicillin.
A Study of Antibacterial Activity of Some Novel 8-Methoxy-4-methyl-quinoline Derivatives
Sheoraj Singh,Vikas Kumar,Ashok Kumar,Shalabh Sharma,Piyush Dua 대한화학회 2010 Bulletin of the Korean Chemical Society Vol.31 No.12
In the present study, some quinoline derivatives have been synthesized like 8-methoxy-4-methyl-2-amino-(3'-chloro-2'-oxo-4'-substituted aryl-1'-azetidinyl)quinolines 8-12 and 8-methoxy-4-methyl-2-amino-(2'-substituted aryl-4'-oxo-1',3'-thiazolidin-3'-yl) quinolines 13-17 from 8-methoxy-4-methyl-2-substituted arylidenyliminoamino)-quinolines 3-7. The structural assignments of these compounds were based on spectral (IR, 1H-NMR, Mass) and elemental (C, H,N) analysis. Further, these compounds were evaluated for antibacterial activity against various bacterial strains. Three compounds 10, 11 and 16 were found to exhibit potent antibacterial activity as compared to the standard drug amphicillin.