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dc.contributor.author류재상-
dc.date.accessioned2016-08-28T12:08:30Z-
dc.date.available2016-08-28T12:08:30Z-
dc.date.issued2012-
dc.identifier.issn0040-4020-
dc.identifier.otherOAK-8866-
dc.identifier.urihttp://dspace.ewha.ac.kr/handle/2015.oak/222719-
dc.description.abstractCatalytic intramolecular additions of hydroxyl groups to tethered conjugated dienes are described. The reactions proceed smoothly at 60 °C in the presence of 5 mol % of (PPh 3)AuCl/AgOTf as a catalyst. A broad range of structurally diverse conjugated dienes produce substituted tetrahydrofurans and tetrahydropyrans in good yields. This reaction represents an atom-economic route to construct five- and six-membered cyclic ethers. © 2012 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.titleGold-catalyzed intramolecular hydroalkoxylation/cyclization of conjugated dienyl alcohols-
dc.typeArticle-
dc.relation.issue24-
dc.relation.volume68-
dc.relation.indexSCI-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage4805-
dc.relation.lastpage4812-
dc.relation.journaltitleTetrahedron-
dc.identifier.doi10.1016/j.tet.2012.03.120-
dc.identifier.wosidWOS:000304798800029-
dc.identifier.scopusid2-s2.0-84861221977-
dc.author.googleChandrasekhar B.-
dc.author.googleRyu J.-S.-
dc.contributor.scopusid류재상(36081118200)-
dc.date.modifydate20170601153005-
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약학대학 > 약학과 > Journal papers
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