中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Facile Synthesis of Trisubstituted Carbazoles by Acid-Catalyzed Ring-Opening Annulation of 2-Amidodihydrofurans with Indoles

文献类型:期刊论文

作者Zhao JJ(赵静静)1,2; Li P(李盼)1; Xia CG(夏春谷)1; Li FW(李福伟)1; Li FW(李福伟)
刊名Chemistry - A European Journal
出版日期2015
卷号21期号:46页码:16383-16386
关键词acid-catalysis carbazoles chemoselectivity regioselectivity ring-opening annulation
ISSN号0947-6539
通讯作者李福伟
英文摘要A mild and convenient synthesis of carbazoles by TfOTMS (trimethylsilyl trifluoromethanesulfonate)-catalyzed ring-opening annulation of 2-amidodihydrofurans is presented with a high degree of chemoselectivity and regioselectivity. This procedure was also scaled up to a gram-scale synthesis. The reaction could involve an iminonium intermediate through a series of CO, CN bond cleavages, CC bond formations, and a 1,2-migration process.
学科主题物理化学与绿色催化
收录类别SCI
资助信息the Chinese Academy of Science;the National Natural Science Foundation of China (21133011;21373246;21522309)
语种英语
WOS记录号WOS:000365132100013
源URL[http://210.77.64.217/handle/362003/18893]  
专题兰州化学物理研究所_OSSO国家重点实验室
通讯作者Li FW(李福伟)
作者单位1.Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth Oxidat, Lanzhou 730000, Peoples R China
2.Chinese Acad Sci, Grad Univ, Beijing 100049, Peoples R China
推荐引用方式
GB/T 7714
Zhao JJ,Li P,Xia CG,et al. Facile Synthesis of Trisubstituted Carbazoles by Acid-Catalyzed Ring-Opening Annulation of 2-Amidodihydrofurans with Indoles[J]. Chemistry - A European Journal,2015,21(46):16383-16386.
APA Zhao JJ,Li P,Xia CG,Li FW,&李福伟.(2015).Facile Synthesis of Trisubstituted Carbazoles by Acid-Catalyzed Ring-Opening Annulation of 2-Amidodihydrofurans with Indoles.Chemistry - A European Journal,21(46),16383-16386.
MLA Zhao JJ,et al."Facile Synthesis of Trisubstituted Carbazoles by Acid-Catalyzed Ring-Opening Annulation of 2-Amidodihydrofurans with Indoles".Chemistry - A European Journal 21.46(2015):16383-16386.

入库方式: OAI收割

来源:兰州化学物理研究所

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