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dc.contributor.authorLiu, Cheng-Yuanen_US
dc.contributor.authorChen, Ying-Hoen_US
dc.contributor.authorChen, Chih-Haoen_US
dc.contributor.authorYu, Ming-Shiuanen_US
dc.contributor.authorTsai, Fu-Yuen_US
dc.contributor.authorOng, Tiow-Ganen_US
dc.date.accessioned2019-04-03T06:39:48Z-
dc.date.available2019-04-03T06:39:48Z-
dc.date.issued2016-09-01en_US
dc.identifier.issn0039-7881en_US
dc.identifier.urihttp://dx.doi.org/10.1055/s-0035-15661438en_US
dc.identifier.urihttp://hdl.handle.net/11536/134269-
dc.description.abstractA catalytic paradigm is described featuring a synergistic interaction between nickel, aluminum and different ligands to impart a rather remote C-H alkenylation of imidazo[1,5-a] pyridines at the C-8 position without the necessity of installing a directing group. The scope of the direct C-H activation reactions of various 5-aryl- and 3-arylimidazopyridines is established using different sterically hindered alkynes.en_US
dc.language.isoen_USen_US
dc.subjectC-H activationen_US
dc.subjectnickelen_US
dc.subjectaluminumen_US
dc.subjectimidazopyridinesen_US
dc.subjectcooperative catalysisen_US
dc.titleSelective C(8)-H Activation of Imidazopyridines Mediated by Cooperative Nickel-Aluminum Catalysisen_US
dc.typeArticleen_US
dc.identifier.doi10.1055/s-0035-15661438en_US
dc.identifier.journalSYNTHESIS-STUTTGARTen_US
dc.citation.volume48en_US
dc.citation.issue17en_US
dc.citation.spage2781en_US
dc.citation.epage2788en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000384022700008en_US
dc.citation.woscount1en_US
Appears in Collections:Articles


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