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dc.contributor.authorHao, Luzh_CN
dc.contributor.authorPan, Yingmingzh_CN
dc.contributor.authorWang, Taozh_CN
dc.contributor.authorLin, Minzh_CN
dc.contributor.authorChen, Lizh_CN
dc.contributor.authorZhan, Zhuang-pingzh_CN
dc.contributor.author陈亮zh_CN
dc.date.accessioned2013-12-12T02:24:28Z
dc.date.available2013-12-12T02:24:28Z
dc.date.issued2010-12-17zh_CN
dc.identifier.citationAdvanced Synthesis & Catalysis, 2010,352(18):3215-3222zh_CN
dc.identifier.issn1615-4150zh_CN
dc.identifier.otherISI:000285397800021zh_CN
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/65567
dc.descriptionNational Natural Science Foundation of China [20772098, 21072159]zh_CN
dc.description.abstractAn efficient cascade methodology toward chemoselective synthesis of N-fused heterocycles including 9H-pyrrolo[1,2-a] indole, 3H-pyrrolo[1,2-a]indole and 1H-pyrrolo[1,2-a]indole derivatives has been developed. This transformation proceeds via a silver(I) triflate-catalyzed consecutive Friedel-Crafts reaction/N-C bond formation sequence between readily available propargyl alcohols and 3-substituted 1H-indoles. Not only is excellent chemoselectivity observed according to the substitution patterns of propargyl alcohols, but also the Lewis acid-catalyzed N-C bond formation process can be carried out under base- and ligand-free conditions.zh_CN
dc.language.isoen_USzh_CN
dc.source.urihttp://dx.doi.org/10.1002/adsc.201000525zh_CN
dc.subjectONE-POT SYNTHESISzh_CN
dc.subjectFECL3-CATALYZED NUCLEOPHILIC-SUBSTITUTIONzh_CN
dc.subjectAZIDE CYCLOADDITION CHEMISTRYzh_CN
dc.subjectPROPARGYLIC ALCOHOLSzh_CN
dc.subjectAROMATIC-COMPOUNDSzh_CN
dc.subjectTANDEM REACTIONzh_CN
dc.subjectDERIVATIVESzh_CN
dc.subjectINDOLESzh_CN
dc.subjectCATIONSzh_CN
dc.subjectFURANSzh_CN
dc.titleChemoselective Cascade Synthesis of N-Fused Heterocycles via Silver(I) Triflate-Catalyzed Friedel-Crafts/N-C Bond Formation Sequencezh_CN
dc.typeArticlezh_CN


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