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dc.contributor.authorLu, Qingen_US
dc.contributor.authorXin Huangen_US
dc.contributor.authorSong, Gonghuaen_US
dc.contributor.authorSun, Chung-Mingen_US
dc.contributor.authorJasinski, Jerry P.en_US
dc.contributor.authorKeeley, Amanda C.en_US
dc.contributor.authorZhang, Weien_US
dc.date.accessioned2014-12-08T15:31:12Z-
dc.date.available2014-12-08T15:31:12Z-
dc.date.issued2013-07-01en_US
dc.identifier.issn2156-8952en_US
dc.identifier.urihttp://dx.doi.org/10.1021/co400026sen_US
dc.identifier.urihttp://hdl.handle.net/11536/22221-
dc.description.abstractA strategy of combining [3 + 2] cycloaddition and intramolecular Diels-Alder reaction is developed for the [3 + 2] cycloaddition of azomethine ylides and maleimides were derivatized for intramolecular Diels-Alder reaction of furan to form highly condensed heterocyclic products as racemic single diastereomers.en_US
dc.language.isoen_USen_US
dc.subjectsequential cycloadditionsen_US
dc.subjectstereoselective annulationen_US
dc.subject[3+2] cycloadditionen_US
dc.subjectintramolecular Diels-Alder reactionen_US
dc.subjectpolyheterocyclic scaffolden_US
dc.titleSequential [3+2] and [4+2] Cycloadditions for Stereoselective Synthesis of a Novel Polyheterocyclic Scaffolden_US
dc.typeArticleen_US
dc.identifier.doi10.1021/co400026sen_US
dc.identifier.journalACS COMBINATORIAL SCIENCEen_US
dc.citation.volume15en_US
dc.citation.issue7en_US
dc.citation.spage350en_US
dc.citation.epage355en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000321793500005-
dc.citation.woscount0-
Appears in Collections:Articles


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