完整後設資料紀錄
DC 欄位語言
dc.contributor.authorDhole, Sandipen_US
dc.contributor.authorChiu, Wei-Jungen_US
dc.contributor.authorSun, Chung-Mingen_US
dc.date.accessioned2019-09-02T07:46:19Z-
dc.date.available2019-09-02T07:46:19Z-
dc.date.issued2019-06-18en_US
dc.identifier.issn1615-4150en_US
dc.identifier.urihttp://dx.doi.org/10.1002/adsc.201900088en_US
dc.identifier.urihttp://hdl.handle.net/11536/152701-
dc.description.abstractCatalyst-controlled chemodivergent annulation between o-indolo anilines and diazo compounds has explored for the synthesis of indolo-fused diazepine and quinoxaline Under the Rh(III) catalyst, reaction proceeded through the free amine assisted C2-H activation followed by amidation leading to the diazepino [1,7-alpha]indole in a highly selective manner. While with Ru(II) catalyst, reaction involves formation Ru-carbene complex followed by -NH2 group insertion and cascade cyclization via metallo-ene type reaction, beta-hydride elimination to furnish the indolo[1,2-alpha]quinoxaline as the predominating product. This strategy directs modular approach towards the construction of unique indolo-fused diazepine/quinoxaline as well as pyrrolo-fused diazepine/quinoxaline scaffolds in excellent yields.en_US
dc.language.isoen_USen_US
dc.subjectCatalyst-controlleden_US
dc.subjectChemodivergent Annulationen_US
dc.subjectIndolo/Pyrrolo-Fused Diazepine and Quinoxalineen_US
dc.titleCatalyst-Controlled Chemodivergent Annulation to Indolo/Pyrrolo-Fused Diazepine and Quinoxalineen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/adsc.201900088en_US
dc.identifier.journalADVANCED SYNTHESIS & CATALYSISen_US
dc.citation.volume361en_US
dc.citation.issue12en_US
dc.citation.spage2916en_US
dc.citation.epage2925en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000478036100015en_US
dc.citation.woscount0en_US
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