Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/33894
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dc.contributor.authorKao, Hsin-Lunen_US
dc.contributor.authorChen, Chin-Kengen_US
dc.contributor.authorWang, Yu-Jenen_US
dc.contributor.authorLee, Chin-Faen_US
dc.contributor.other國立中興大學化學系zh_TW
dc.contributor.otherNational Chung Hsing University,Department of Chemistryen_US
dc.date2011-3zh_TW
dc.date.accessioned2014-06-06T07:46:51Z-
dc.date.available2014-06-06T07:46:51Z-
dc.identifier.issn1434-193Xzh_TW
dc.identifier.urihttp://hdl.handle.net/11455/33894-
dc.description.abstractCommercially available Cu(2)O powder is a very reactive catalyst for the coupling of thiols to aryl iodides. A variety of functional groups including esters, unprotected amines, alcohols, and heterocycles tolerate the reaction conditions. Moreover, di-ortho-substituted aryl iodides with sterically demanding substrates were also coupled to give the desired aryl thioethers in good to excellent yields.en_US
dc.language.isoen_USzh_TW
dc.relationEuropean Journal of Organic Chemistry, Issue 9, Page(s) 1776-1781.en_US
dc.subjectCopperen_US
dc.subjectCross-couplingen_US
dc.subjectSulfuren_US
dc.subjectThioethersen_US
dc.subjectHomogeneous catalysisen_US
dc.subjectsulfur bond formationen_US
dc.subjectc-sen_US
dc.subjectnucleophilic-substitutionen_US
dc.subjectboronic acidsen_US
dc.subjectpalladiumen_US
dc.subjecthalidesen_US
dc.subjectliganden_US
dc.subjectarylationen_US
dc.subjectcomplexesen_US
dc.subjectoxideen_US
dc.titleAn Efficient Copper-Catalyzed Cross-Coupling Reaction of Thiols with Aryl Iodidesen_US
dc.typeJournal Articlezh_TW
dc.identifier.doi10.1002/ejoc.201001667zh_TW
dc.contributor.catalogerMiao-zhen Luoen_US
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