完整後設資料紀錄
DC 欄位語言
dc.contributor.authorDhole, Sandipen_US
dc.contributor.authorSun, Chung-Mingen_US
dc.date.accessioned2019-04-02T06:00:30Z-
dc.date.available2019-04-02T06:00:30Z-
dc.date.issued2019-02-01en_US
dc.identifier.issn1615-4150en_US
dc.identifier.urihttp://dx.doi.org/10.1002/adsc.201801241en_US
dc.identifier.urihttp://hdl.handle.net/11536/148827-
dc.description.abstractA facile and straightforward synthesis of benzoimidazo[2,1-a]isoquinolines through Ru(II)-catalyzed [4+2] annulation reaction of 2-aryl benzimidazole and styrene has been explored. Tentative mechanistic studies imply the current reaction involves sequential C-C/C-N bond formation through the ortho C-H activation of 2-aryl benzimidazole followed by C-N reductive elimination. This newly developed strategy is widely applicable and tolerates various 2-arylbenzimidazole and vinyl derivatives, and allows the attractive vehicle for direct construction of diverse C6-substituated benzoimidazoisoquinoline scaffold in good yields.en_US
dc.language.isoen_USen_US
dc.subjectBenzoimidazo[2,1-a]isoquinolines Rutheniumen_US
dc.subject[4+2] annulationen_US
dc.subject2-aryl benzimidazoleen_US
dc.subjectStyreneen_US
dc.titleDirect Access to Dihydrobenzoimidazo[2,1-a]isoquinolines through Ruthenium-catalyzed Formal [4+2] Annulationen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/adsc.201801241en_US
dc.identifier.journalADVANCED SYNTHESIS & CATALYSISen_US
dc.citation.volume361en_US
dc.citation.spage535en_US
dc.citation.epage541en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000457795500021en_US
dc.citation.woscount0en_US
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