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dc.contributor.authorChen, Chih-Hauen_US
dc.contributor.authorYellol, Gorakh S.en_US
dc.contributor.authorLin, Po-Tsungen_US
dc.contributor.authorSun, Chung-Mingen_US
dc.date.accessioned2014-12-08T15:20:43Z-
dc.date.available2014-12-08T15:20:43Z-
dc.date.issued2011-10-07en_US
dc.identifier.issn1523-7060en_US
dc.identifier.urihttp://dx.doi.org/10.1021/ol201985pen_US
dc.identifier.urihttp://hdl.handle.net/11536/14744-
dc.description.abstractA novel base-catalyzed Povarov reaction of arylamines, aldehydes, and electron-deficient dienophiles has been developed. An unprecedented in situ [1,3] sigmatropic rearrangement leading to 4,10-dihydropyrimido[1,2-a]benzimidazoles has also been discovered. An insight of the plausible mechanism is discussed and supported by X-ray crystal study. This cascade reaction is achieved in a one-pot multicomponent fashion on soluble support under microwave conditions.en_US
dc.language.isoen_USen_US
dc.titleBase-Catalyzed Povarov Reaction: An Unusual [1,3] Sigmatropic Rearrangement to Dihydropyrimidobenzimidazolesen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/ol201985pen_US
dc.identifier.journalORGANIC LETTERSen_US
dc.citation.volume13en_US
dc.citation.issue19en_US
dc.citation.spage5120en_US
dc.citation.epage5123en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000295313900037-
dc.citation.woscount13-
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