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dc.contributor.authorAnnamalai, Pratheepkumaren_US
dc.contributor.authorChen, Wu-Yinen_US
dc.contributor.authorRaju, Selvamen_US
dc.contributor.authorHsu, Kou-Chien_US
dc.contributor.authorUpadhyay, Nitinkumar Satyadeven_US
dc.contributor.authorCheng, Chien-Hongen_US
dc.contributor.authorChuang, Shih-Chingen_US
dc.date.accessioned2017-04-21T06:55:24Z-
dc.date.available2017-04-21T06:55:24Z-
dc.date.issued2016-11-17en_US
dc.identifier.issn1615-4150en_US
dc.identifier.urihttp://dx.doi.org/10.1002/adsc.201600488en_US
dc.identifier.urihttp://hdl.handle.net/11536/133000-
dc.description.abstractPalladium-catalyzed cycloaromatization of N-acyl-2-aminobiaryls, through a sequence of ortho C-H bond activation/alkyne insertion/meta C-H bond activation/alkyne insertion, was developed. An efficient synthesis of multiaryl-substituted naphthalenes, N-[2-(5,6,7,8-tetraarylnaphthalen-1-yl) aryl] acetamides, was demonstrated using molecular oxygen as the sole oxidant. Furthermore, through Buchwald\'s synthetic protocol, two compounds were converted into corresponding fluorescent carbazoles in 30-40% yield by intramolecular C-N bond formation.en_US
dc.language.isoen_USen_US
dc.subjectalkynesen_US
dc.subjectaromatic homologationen_US
dc.subjectC-H activationen_US
dc.subjectnaphthalenesen_US
dc.subjectpalladiumen_US
dc.titlePalladium-Catalyzed Selective Aryl Ring C-H Activation of N-Acyl-2-aminobiaryls: Efficient Access to Multiaryl-Substituted Naphthalenesen_US
dc.identifier.doi10.1002/adsc.201600488en_US
dc.identifier.journalADVANCED SYNTHESIS & CATALYSISen_US
dc.citation.volume358en_US
dc.citation.issue22en_US
dc.citation.spage3642en_US
dc.citation.epage3648en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000390408200016en_US
Appears in Collections:Articles