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dc.contributor.authorNarhe, Bharat D.en_US
dc.contributor.authorTsai, Min-Huanen_US
dc.contributor.authorSun, Chung-Mingen_US
dc.date.accessioned2019-04-02T06:00:06Z-
dc.date.available2019-04-02T06:00:06Z-
dc.date.issued2014-08-01en_US
dc.identifier.issn2156-8952en_US
dc.identifier.urihttp://dx.doi.org/10.1021/co500049ren_US
dc.identifier.urihttp://hdl.handle.net/11536/147783-
dc.description.abstractA two-step, three-component coupling reaction on ionic liquid supported 2-cyanomethylbenzimidazoles, methyl 2-formylbenzoate, and isocyanides under microwave activation is explored. Knoevenagel condensation of 2-cyanomethylbenzimidazole with methyl-2-formylbenzoate in the presence of piperidine catalyst is followed by [4 + 1] cycloaddition with an isocyanide in the next step. Consequent intramolecular delta-lactam formation allows rapid construction of novel aza-pentacycles, benzimidazo [1',2':1,5]pyrrolo [2,3-c]isoquinolines.en_US
dc.language.isoen_USen_US
dc.subjectmicrowaveen_US
dc.subjectionic liquid supporten_US
dc.subjectpyrrolo[1,2-a]benzimidazoleen_US
dc.subjectbenzimidazo[1',2':1,5]pyrrolo[2,3-c]isoquinolinesen_US
dc.titleRapid Two-Step Synthesis of Benzimidazo[1 ',2 ':1,5]-pyrrolo[2,3-c]isoquinolines by a Three-Component Coupling Reactionen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/co500049ren_US
dc.identifier.journalACS COMBINATORIAL SCIENCEen_US
dc.citation.volume16en_US
dc.citation.spage421en_US
dc.citation.epage427en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000340344500008en_US
dc.citation.woscount10en_US
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