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Studies on Semisynthesis and Anibacterial Activity of 7 β-(5-Methyl-1-Aryl-1H-1,2,3-Triazoly-4-Carboxamido) Cephalosporins
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作者 Zi Yi ZHANG Yu Xiang LIANG(National Laboratory of Applied Organic Chemistry, Department of Chemistry,Lanzhou University, Lanzhou 73000)Zuo Wu GUAN(Institute of Applied Pharmacy, Beijing Medical University, Beijing 100083) 《Chinese Chemical Letters》 SCIE CAS CSCD 1997年第4期295-298,共4页
Nine new derivatives of 7 β - (5- methyl- 1- aryl- 1H-1, 2, 3- triazoly- 4- carboxamido) cephalosporins were synthesized by acylction of 7 β -amino group of 7-ACA, 7-ADCA and 7-ACT with 5 -methsyl- 1 -aryl- 1 H- 1,2... Nine new derivatives of 7 β - (5- methyl- 1- aryl- 1H-1, 2, 3- triazoly- 4- carboxamido) cephalosporins were synthesized by acylction of 7 β -amino group of 7-ACA, 7-ADCA and 7-ACT with 5 -methsyl- 1 -aryl- 1 H- 1,2,3-triazoly-4-formyl chloride. The structure of the compounds were confirmed by elementray analysis IR, HNMR and FAB-MS. Some of them showed significant antibacterial activity 展开更多
关键词 Activity MS FAB Studies on Semisynthesis and anibacterial Activity of 7 CEPHALOSPORINS Methyl-1-Aryl-1H-1 2 3-Triazoly-4-Carboxamido
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