中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Electrophile-driven regioselective synthesis of functionalized quinolines

文献类型:期刊论文

作者Ali Shaukat; Zhu HT(祝海涛); Xia XF(夏晓峰); Ji KG(纪克攻); Yang YF(杨艳芳); Song XR(宋贤荣); Liang YM(梁永民)
刊名J. Org. Lett.
出版日期2011
卷号13期号:10页码:2598-2601
ISSN号0022-3263
通讯作者梁永民
中文摘要Highly substituted 3-iodoquinolines bearing different alkyl and aryl moieties can be synthesized in moderate to excellent yields (up to 99%) by 6-endo-dig iodocyclization of 2-tosylaminophenylprop-1-yn-3-ols with molecular iodine (I2) under mild conditions. The cyclization is highly regioselective and the resulting 3-iodoquinolines can be further functionalized by various coupling reactions.
学科主题材料科学与物理化学
收录类别SCI
资助信息the National Science Foundation (NSF-21072080);the National Basic Research Program of China (973 Program),2010CB833203
语种英语
WOS记录号WOS:000290465800023
公开日期2013-10-15
源URL[http://210.77.64.217/handle/362003/3963]  
专题兰州化学物理研究所_固体润滑国家重点实验室
推荐引用方式
GB/T 7714
Ali Shaukat,Zhu HT,Xia XF,et al. Electrophile-driven regioselective synthesis of functionalized quinolines[J]. J. Org. Lett.,2011,13(10):2598-2601.
APA Ali Shaukat.,Zhu HT.,Xia XF.,Ji KG.,Yang YF.,...&Liang YM.(2011).Electrophile-driven regioselective synthesis of functionalized quinolines.J. Org. Lett.,13(10),2598-2601.
MLA Ali Shaukat,et al."Electrophile-driven regioselective synthesis of functionalized quinolines".J. Org. Lett. 13.10(2011):2598-2601.

入库方式: OAI收割

来源:兰州化学物理研究所

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