中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Expeditious one-pot synthesis of C3-piperazinyl-substituted quinolines: key precursors to potent c-Met inhibitors

文献类型:期刊论文

作者Wang, Yuanxiang2; Ai, Jing1; Liu, Gang2; Geng, Meiyu1; Zhang, Ao2
刊名ORGANIC & BIOMOLECULAR CHEMISTRY
出版日期2011
卷号9期号:17页码:5930-5933
ISSN号1477-0520
DOI10.1039/c1ob05830d
文献子类Article
英文摘要An effective one-pot synthesis of quinolines bearing diverse C3-piperazinyl functions was developed by using a modified Friedlander's protocol. The method not only enables the synthesis of our early reported c-Met inhibitor on a large scale, but also provides a way to generate novel multi-substituted quinolines for further structure-activity relationship (SAR) study.
WOS关键词KINASE ; OPTIMIZATION ; DISCOVERY
WOS研究方向Chemistry
语种英语
出版者ROYAL SOC CHEMISTRY
WOS记录号WOS:000293756800004
源URL[http://119.78.100.183/handle/2S10ELR8/278672]  
专题药理学第一研究室
药物化学研究室
通讯作者Geng, Meiyu
作者单位1.Chinese Acad Sci, Div Antitumor Pharmacol, SIMM, Shanghai 201203, Peoples R China;
2.Chinese Acad Sci, Synthet Organ & Med Chem Lab, SIMM, Shanghai 201203, Peoples R China
推荐引用方式
GB/T 7714
Wang, Yuanxiang,Ai, Jing,Liu, Gang,et al. Expeditious one-pot synthesis of C3-piperazinyl-substituted quinolines: key precursors to potent c-Met inhibitors[J]. ORGANIC & BIOMOLECULAR CHEMISTRY,2011,9(17):5930-5933.
APA Wang, Yuanxiang,Ai, Jing,Liu, Gang,Geng, Meiyu,&Zhang, Ao.(2011).Expeditious one-pot synthesis of C3-piperazinyl-substituted quinolines: key precursors to potent c-Met inhibitors.ORGANIC & BIOMOLECULAR CHEMISTRY,9(17),5930-5933.
MLA Wang, Yuanxiang,et al."Expeditious one-pot synthesis of C3-piperazinyl-substituted quinolines: key precursors to potent c-Met inhibitors".ORGANIC & BIOMOLECULAR CHEMISTRY 9.17(2011):5930-5933.

入库方式: OAI收割

来源:上海药物研究所

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