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dc.contributor.authorLin, Yu-Weien_US
dc.contributor.authorDeng, Jie-Chengen_US
dc.contributor.authorHsieh, You-Zungen_US
dc.contributor.authorChuang, Shih-Chingen_US
dc.date.accessioned2014-12-08T15:34:34Z-
dc.date.available2014-12-08T15:34:34Z-
dc.date.issued2014-01-07en_US
dc.identifier.issn1477-0520en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c3ob41811aen_US
dc.identifier.urihttp://hdl.handle.net/11536/23606-
dc.description.abstractWe demonstrate a straightforward synthesis of gamma-lactams possessing an a-phosphorus Aide moiety from assembly of phosphines, N-tosyl aldimines and an enyne through an initial alpha(delta')-attack of phosphines to an enyne in up to 79% yield. The investigated multicomponent reaction tolerates a variety of triaryl-phosphines and electron-poor aldimines to give gamma-lactams in one pot. One of the lactams, with the tri(p-tol)phosphine and 4-cyanophenyl moiety, exhibits fluorescence emission at 447 nm with a quantum yield of 0.11.en_US
dc.language.isoen_USen_US
dc.titleOne-pot formation of fluorescent gamma-lactams having an alpha-phosphorus ylide moiety through three-component alpha(delta ')-Michael reactions of phosphines with an enyne and N-tosyl aldiminesen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c3ob41811aen_US
dc.identifier.journalORGANIC & BIOMOLECULAR CHEMISTRYen_US
dc.citation.volume12en_US
dc.citation.issue1en_US
dc.citation.spage162en_US
dc.citation.epage170en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000329551100019-
dc.citation.woscount4-
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