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dc.contributor.authorLee, Wei-Chihen_US
dc.contributor.authorChen, Chien-Hungen_US
dc.contributor.authorLiu, Cheng-Yuanen_US
dc.contributor.authorYu, Ming-Shiuanen_US
dc.contributor.authorLin, Yung-Hueien_US
dc.contributor.authorOng, Tiow-Ganen_US
dc.date.accessioned2016-03-28T00:04:22Z-
dc.date.available2016-03-28T00:04:22Z-
dc.date.issued2015-01-01en_US
dc.identifier.issn1359-7345en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c5cc07455jen_US
dc.identifier.urihttp://hdl.handle.net/11536/129599-
dc.description.abstractpara-CH activation of pyridine with allylbenzene is described by Ni/Al cooperative catalysis in combination with a bulkier NHC ligand and a Lewis acid, leading to linear hydroheteroarylation products. Interestingly, the branch selectivity can be achieved by using the combination of a less sterically hindered amino-NHC ligand and AlMe3 through tandem reaction of facile alkene isomerization followed by a slow CH bond activation process.en_US
dc.language.isoen_USen_US
dc.titleNickel-catalysed para-CH activation of pyridine with switchable regioselective hydroheteroarylation of allylarenesen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c5cc07455jen_US
dc.identifier.journalCHEMICAL COMMUNICATIONSen_US
dc.citation.volume51en_US
dc.citation.issue96en_US
dc.citation.spage17104en_US
dc.citation.epage17107en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000367469400012en_US
dc.citation.woscount0en_US
Appears in Collections:Articles