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dc.contributor.author오창호-
dc.date.accessioned2018-03-12T06:08:14Z-
dc.date.available2018-03-12T06:08:14Z-
dc.date.issued2013-06-
dc.identifier.citationChemistry - A European Journal. (Chemistry - A European Journal, 5 August 2013, 19(32), P.10501-10505en_US
dc.identifier.issn0947-6539-
dc.identifier.urihttp://onlinelibrary.wiley.com/doi/10.1002/chem.201301384/full-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/45420-
dc.description.abstractA new Au-catalyzed cascade reaction was developed for the conversion of propargylic acetates 1 to benzannulated products 2 in good to excellent yields. The gold catalyst is involved in generating intermediate A and in the ene-type reaction of intermediate B for the formation of product 2 (see scheme).en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectcarbenesen_US
dc.subjectcatalysisen_US
dc.subjectcycloisomerizationen_US
dc.subjectene reactionen_US
dc.subjectgolden_US
dc.subjectpropargyl carboxylateen_US
dc.titleGold Carbenes from Substituted Propargyl Acetates: Intramolecular Ene-type Reactions to 2-Acetoxynaphthalene Derivativesen_US
dc.typeArticleen_US
dc.relation.no32-
dc.relation.volume19-
dc.identifier.doi10.1002/chem.201301384-
dc.relation.page10501-10505-
dc.relation.journalCHEMISTRY-A EUROPEAN JOURNAL-
dc.contributor.googleauthorOh, C.H.-
dc.contributor.googleauthorKim, J.H-
dc.contributor.googleauthorPiao, L.-
dc.contributor.googleauthorYu, J.-
dc.contributor.googleauthorKim, S.Y-
dc.relation.code2013009401-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF NATURAL SCIENCES[S]-
dc.sector.departmentDEPARTMENT OF CHEMISTRY-
dc.identifier.pidchangho-
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COLLEGE OF NATURAL SCIENCES[S](자연과학대학) > CHEMISTRY(화학과) > Articles
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