Zobrazeno 1 - 4
of 4
pro vyhledávání: '"K. H. Deitcher"'
Autor:
Fred Konzelmann, Harry Allen Albrecht, Chung Chen Wei, G. Beskid, J. G. Christenson, N H Georgopapadakou, Dennis D. Keith, David L. Pruess, K. H. Deitcher
Publikováno v:
Journal of Medicinal Chemistry. 37:400-407
We have previously reported that linking quinolones to the cephalosporin 3'-position through an ester bond, a carbamate function, or a bond through a quaternary nitrogen produced cephalosporins with a dual mode of antibacterial action. We now describ
Autor:
N H Georgopapadakou, Chung Chen Wei, Dennis D. Keith, G. Beskid, J. G. Christenson, Fred Konzelmann, Harry Allen Albrecht, K. H. Deitcher, David L. Pruess
Publikováno v:
ChemInform. 25
We have previously reported that linking quinolones to the cephalosporin 3'-position through an ester bond, a carbamate function, or a bond through a quaternary nitrogen produced cephalosporins with a dual mode of antibacterial action. We now describ
Autor:
Sepinwall J, R. Cleeland, Chan Ka-Kong, J. G. Christenson, Dennis D. Keith, Harry Allen Albrecht, G. Beskid, K. H. Deitcher, N H Georgopapadakou, David L. Pruess
Publikováno v:
Journal of Medicinal Chemistry. 33:77-86
According to the generally accepted mechanism by which bacterial enzymes react with cephalosporins, opening of the beta-lactam ring can lead to the expulsion of a 3'-substituent. A series of dual-action cephalosporins was prepared in which antibacter
Publikováno v:
Synthesis. 1977:492-494