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Reactions of Aryl 5-Substituted-2-Thiophenecarboxylate Promoted by 4-Z-C6H4O-/4-Z-C6H4OH in 20 mol% DMSO(aq). Effect of Nucleophile on the Acyl Transfer Reaction (vol 36, pg 2810, 2015)

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dc.contributor.authorPyun, Sang Yong-
dc.contributor.authorPaik, Kyu Cheol-
dc.contributor.authorHan, Man So-
dc.contributor.authorCho, Bong Rae-
dc.date.accessioned2021-09-04T02:24:28Z-
dc.date.available2021-09-04T02:24:28Z-
dc.date.created2021-06-16-
dc.date.issued2016-03-
dc.identifier.issn0253-2964-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/89456-
dc.languageEnglish-
dc.language.isoen-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.titleReactions of Aryl 5-Substituted-2-Thiophenecarboxylate Promoted by 4-Z-C6H4O-/4-Z-C6H4OH in 20 mol% DMSO(aq). Effect of Nucleophile on the Acyl Transfer Reaction (vol 36, pg 2810, 2015)-
dc.typeArticle-
dc.contributor.affiliatedAuthorCho, Bong Rae-
dc.identifier.doi10.1002/bkcs.10694-
dc.identifier.scopusid2-s2.0-84960119480-
dc.identifier.wosid000371907500031-
dc.identifier.bibliographicCitationBULLETIN OF THE KOREAN CHEMICAL SOCIETY, v.37, no.3, pp.422 - 422-
dc.relation.isPartOfBULLETIN OF THE KOREAN CHEMICAL SOCIETY-
dc.citation.titleBULLETIN OF THE KOREAN CHEMICAL SOCIETY-
dc.citation.volume37-
dc.citation.number3-
dc.citation.startPage422-
dc.citation.endPage422-
dc.type.rimsART-
dc.type.docTypeCorrection-
dc.identifier.kciidART002089423-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordAuthorNucleophilic substitution-
dc.subject.keywordAuthorBronsted and Hammett plots-
dc.subject.keywordAuthorConcerted and stepwise mechanism-
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