Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/34676
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dc.contributor.authorChen, H.H.en_US
dc.contributor.author陳耀鐘zh_TW
dc.contributor.authorHuang, H.M.en_US
dc.contributor.authorChen, S.C.en_US
dc.contributor.authorChen, Y.J.en_US
dc.date2010zh_TW
dc.date.accessioned2014-06-06T07:48:08Z-
dc.date.available2014-06-06T07:48:08Z-
dc.identifier.issn0009-4536zh_TW
dc.identifier.urihttp://hdl.handle.net/11455/34676-
dc.description.abstractAn efficient copper-catalyzed N-arylation of azaheterocycles with aryl iodides using 1,1,1-tris(hydroxymethyl)ethane as a tridentates O-donor ligand has been accomplished in good to excellent yields. Moreover, this highly efficient catalyst system has been successfully demonstrated to one-step synthesis of toloxatone and a shorter route to formal synthesis of linezolid in good yields.en_US
dc.language.isoen_USzh_TW
dc.relationJournal of the Chinese Chemical Societyen_US
dc.relation.ispartofseriesJournal of the Chinese Chemical Society, Volume 57, Issue 1, Page(s) 14-18.en_US
dc.subjectCopperen_US
dc.subjectCross-couplingen_US
dc.subjectN-Arylationen_US
dc.subjectAzaheterocyclesen_US
dc.subject1,1,1-Tris(hydroxymethyl)ethaneen_US
dc.subjectnitrogen-containing heterocyclesen_US
dc.subjectcross-coupling reactionsen_US
dc.subjectc-nen_US
dc.subjectbonden_US
dc.subjectformationen_US
dc.subjectheteroaryl halidesen_US
dc.subjectarylboronic acidsen_US
dc.subjectmild conditionsen_US
dc.subjectcopperen_US
dc.subjectimidazolesen_US
dc.subject3-aryl-2-oxooxazolidinesen_US
dc.titleHighly Efficient Cul-catalyzed N-Arylation of Azaheterocycles with Aryl Iodides Using 1,1,1-Tris(hydroxymethyl)ethane as a Tridentate O-Donor Ligand: A Shorter Route to Toloxatone and Formal Synthesis of Linezoliden_US
dc.typeJournal Articlezh_TW
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