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dc.contributor.author김영미-
dc.contributor.author이상기-
dc.date.accessioned2016-08-28T12:08:11Z-
dc.date.available2016-08-28T12:08:11Z-
dc.date.issued2009-
dc.identifier.issn1477-0520-
dc.identifier.otherOAK-5447-
dc.identifier.urihttp://dspace.ewha.ac.kr/handle/2015.oak/220147-
dc.description.abstractAn effective and general route for the regioselective synthesis of 1-phenylpyrazoles has been developed from β-enaminoketoesters prepared by tandem Blaise-acylation. This method is applicable to a very broad range of substrates, generating a diverse set of 3-aryl-5-alkyl, 3-alkyl-5-aryl, 3,5-diaryl, and 3,5-dialkyl substituted pyrazoles regioselectively. The dichotomous regioselective synthesis of isotopically discriminated 3-CD 3-5-CH 3 and 3-CH 3-5-CD 3 substituted pyrazoles showcases the power of this protocol. © The Royal Society of Chemistry 2009.-
dc.languageEnglish-
dc.titleAn effective and general method for the highly regioselective synthesis of 1-phenylpyrazoles from β-enaminoketoesters, tandem Blaise-acylation adducts-
dc.typeArticle-
dc.relation.issue6-
dc.relation.volume7-
dc.relation.indexSCI-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage1132-
dc.relation.lastpage1136-
dc.relation.journaltitleOrganic and Biomolecular Chemistry-
dc.identifier.doi10.1039/b820324e-
dc.identifier.wosidWOS:000263922700014-
dc.identifier.scopusid2-s2.0-62249157813-
dc.author.googleKo Y.O.-
dc.author.googleChun Y.S.-
dc.author.googlePark C.-L.-
dc.author.googleKim Y.-
dc.author.googleShin H.-
dc.author.googleAhn S.-
dc.author.googleHong J.-
dc.author.googleLee S.-G.-
dc.contributor.scopusid김영미(8361744900)-
dc.contributor.scopusid이상기(15082786300)-
dc.date.modifydate20201102081004-
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자연과학대학 > 화학·나노과학전공 > Journal papers
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