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Synthesis of derivatives of imidazo[4,5-b]pyridine: Novel sulfur contained side chains for macrolide antibiotics
作者姓名:Lu  Liu  Peng  Xu  Liang  Zhou  Ping  Sheng  Lei
作者单位:Key Laboratory of Bioactivity Substance and Resources Utilization of Chinese Herbal Medicine, Ministry of Education, Institute of Materia Medica, Peking Union Medical College & Chinese Academy of Medical Science, Beijing 100050, China
基金项目:Finacial support of this research by the National Natural Science Foundation of China (No. 30572275) and Natural Science Foundation of Beijing (No. 7062047) are gratefully acknowledged by the authors.
摘    要:Two series of novel derivatives of imidazo4,5-b]pyridine were synthesized. These compounds could be used as side chains of semisynthesised ketolide antibiotics. The side chains have free amine group which can attached to ketolide core. Macrolides with this kind of side chains will show obvious activities against erythromycin-resistant strains. The structure of the side chains was confirmed by ^1H, ^13C NMR, MS, HMBC spectra. 2007 Ping Sheng Lei. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.

关 键 词:咪唑  嘧啶  大环内酯  合成  杂芳化作用
收稿时间:2007-09-20

Synthesis of derivatives of imidazo[4,5-b]pyridine: Novel sulfur contained side chains for macrolide antibiotics
Lu Liu Peng Xu Liang Zhou Ping Sheng Lei.Synthesis of derivatives of imidazo[4,5-b]pyridine: Novel sulfur contained side chains for macrolide antibiotics[J].Chinese Chemical Letters,2008,19(1):1-4.
Authors:Lu Liu Peng Xu Liang Zhou Ping Sheng Lei
Institution:Key Laboratory of Bioactivity Substance and Resources Utilization of Chinese Herbal Medicine, Ministry of Education, Institute of Materia Medica, Peking Union Medical College & Chinese Academy of Medical Science, Beijing 100050, China
Abstract:Two series of novel derivatives of imidazo4,5-b]pyridine were synthesized. These compounds could be used as side chains of semisynthesised ketolide antibiotics. The side chains have free amine group which can attached to ketolide core. Macrolides with this kind of side chains will show obvious activities against erythromycin-resistant strains. The structure of the side chains was confirmed by ^1H, ^13C NMR, MS, HMBC spectra. 2007 Ping Sheng Lei. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.
Keywords:Macrolide  Heterarylalkyl sulfur contained side chain  Imidazo[4  5-b]pyridine  Synthesis  HMBC
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