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dc.contributor.author이용록ko
dc.contributor.author판딧라메쉬월프라사드ko
dc.date.accessioned2015-12-17T03:55:54Z-
dc.date.available2015-12-17T03:55:54Z-
dc.date.created2015-11-13-
dc.date.issued201410-
dc.identifier.citationADVANCED SYNTHESIS & CATALYSIS, v.356, no.14-15, pp.3171 - 3179-
dc.identifier.issn1615-4150-
dc.identifier.urihttp://hdl.handle.net/YU.REPOSITORY/30642-
dc.identifier.urihttp://dx.doi.org/10.1002/adsc.201400295-
dc.description.abstractThe direct arylation of C(sp(3))-H bonds adjacent to oxygen in ethers with phenol and naphthol derivatives was developed via palladium(II) acetate/copper(II) triflate [Pd(OAc)(2)/Cu(OTf)(2)]-catalyzed cross-dehydrgenative coupling in the presence of tert-butyl hyroperoxide (TBHP). This process provides exclusive installation of a tetrahydrofuranyl moiety at a more hindered position of multiply substituted phenol derivatives. The cross-dehydrogenative coupling of 1,4-dihydroxynaphthalene with cyclic ethers and free alcohols afforded biologically interesting 2-substituted 1,4-naphthoquinone derivatives.-
dc.language영어-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.subjectCROSS-COUPLING REACTIONS-
dc.subjectC-H BONDS-
dc.subjectN-HETEROCYCLIC CARBENES-
dc.subjectACYL-CLAISEN APPROACH-
dc.subjectTRANSITION-METAL-
dc.subjectNATURAL-PRODUCTS-
dc.subjectNAPHTHOQUINONE DERIVATIVES-
dc.subjectSTEREOSELECTIVE-SYNTHESIS-
dc.subjectORGANIC-SYNTHESIS-
dc.subjectFUNCTIONALIZATION-
dc.titleDirect Oxidative Arylation of C(sp(3))-H Bonds Adjacent to Oxygen of Ethers and Alcohols-
dc.typeArticle-
dc.identifier.wosid000342906100035-
dc.identifier.scopusid2-s2.0-84906805149-
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공과대학 > 화학공학부 > Articles
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