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dc.contributor.author윤소원-
dc.date.accessioned2018-03-30T01:14:02Z-
dc.date.available2018-03-30T01:14:02Z-
dc.date.issued2014-04-
dc.identifier.citationOrganic & Biomolecular Chemistry , 2014, 12(15), p.2388-2393en_US
dc.identifier.issn1477-0520-
dc.identifier.issn1477-0539-
dc.identifier.urihttp://pubs.rsc.org/en/Content/ArticleLanding/2014/OB/C3OB42546K#!divAbstract-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/54086-
dc.description.abstractAn efficient NHC-catalyzed domino oxidation/oxa-Michael addition reaction of 2-alkenylbenzaldehydes has been developed to afford 3-substituted phthalides bearing a C3-stereogenic center with a broad substrate scope and wide functional group tolerance. The preliminary results of the asymmetric process have been provided as well.en_US
dc.description.sponsorshipNational Research Foundation of Korea (NRF) Ministry of Education, Science and Technologyen_US
dc.language.isoenen_US
dc.publisherROYAL SOC CHEMISTRY, THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLANDen_US
dc.subjectN-HETEROCYCLIC CARBENEen_US
dc.subjectSTETTER-ALDOL-MICHAELen_US
dc.subjectAROMATIC-ALDEHYDESen_US
dc.subjectAEROBIC CONDITIONSen_US
dc.subjectASYMMETRIC ORGANOCATALYSISen_US
dc.subjectALKYL-HALIDESen_US
dc.subjectESTERIFICATIONen_US
dc.subjectALCOHOLSen_US
dc.subjectACIDen_US
dc.subjectHYDROACYLATIONen_US
dc.titleNHC-catalyzed oxidative cyclization reaction for the synthesis of 3-substituted phthalidesen_US
dc.typeArticleen_US
dc.relation.no15-
dc.relation.volume12-
dc.identifier.doi10.1039/c3ob42546k-
dc.relation.page2388-2393-
dc.relation.journalORGANIC & BIOMOLECULAR CHEMISTRY-
dc.contributor.googleauthorYoun, S.-
dc.contributor.googleauthorSong, H.-
dc.contributor.googleauthorPark, J.-
dc.relation.code2014037105-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF NATURAL SCIENCES[S]-
dc.sector.departmentDEPARTMENT OF CHEMISTRY-
dc.identifier.pidsowony73-
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COLLEGE OF NATURAL SCIENCES[S](자연과학대학) > CHEMISTRY(화학과) > Articles
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