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One for Many: A Universal Reagent for Acylation Processes

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dc.contributor.authorMoon, Hyun Kyung-
dc.contributor.authorSung, Gi Hyeon-
dc.contributor.authorKim, Bo Ram-
dc.contributor.authorPark, Jong Keun-
dc.contributor.authorYoon, Yong-Jin-
dc.contributor.authorYoon, Hyo Jae-
dc.date.accessioned2021-09-03T23:02:56Z-
dc.date.available2021-09-03T23:02:56Z-
dc.date.created2021-06-18-
dc.date.issued2016-06-02-
dc.identifier.issn1615-4150-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/88371-
dc.description.abstractThis work describes acylation reactions facilitated by a type of heterocycle-based acyl transfer agent, 2-acyloxypyridazinone. Reactions of 2-acyloxypyridazinone with carboxylic acids yield mixed carbonic anhydride intermediates, which are reactive and could be coupled with a wide range of substrates including acids, amines, alcohols, and thiols. The wide substrate scope, ease of operation (no additive or catalyst), storage and handling stability, and atom-efficiency from recycling the heterocycle carrier make the reported acylating agent attractive for acylation-based coupling reactions.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.subjectCARBOXYLIC-ACIDS-
dc.subjectORGANIC-SYNTHESIS-
dc.subjectCOUPLING REAGENT-
dc.subjectESTERIFICATION-
dc.subjectCHEMISTRY-
dc.subjectCATALYSIS-
dc.subjectEFFICIENT-
dc.subjectFACILE-
dc.subjectDERIVATIVES-
dc.subjectALCOHOLS-
dc.titleOne for Many: A Universal Reagent for Acylation Processes-
dc.typeArticle-
dc.contributor.affiliatedAuthorYoon, Hyo Jae-
dc.identifier.doi10.1002/adsc.201501177-
dc.identifier.scopusid2-s2.0-84964523758-
dc.identifier.wosid000377267400003-
dc.identifier.bibliographicCitationADVANCED SYNTHESIS & CATALYSIS, v.358, no.11, pp.1725 - 1730-
dc.relation.isPartOfADVANCED SYNTHESIS & CATALYSIS-
dc.citation.titleADVANCED SYNTHESIS & CATALYSIS-
dc.citation.volume358-
dc.citation.number11-
dc.citation.startPage1725-
dc.citation.endPage1730-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Applied-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusCARBOXYLIC-ACIDS-
dc.subject.keywordPlusORGANIC-SYNTHESIS-
dc.subject.keywordPlusCOUPLING REAGENT-
dc.subject.keywordPlusESTERIFICATION-
dc.subject.keywordPlusCHEMISTRY-
dc.subject.keywordPlusCATALYSIS-
dc.subject.keywordPlusEFFICIENT-
dc.subject.keywordPlusFACILE-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordPlusALCOHOLS-
dc.subject.keywordAuthor2-alkoxycarbonylpyridazin-3(2H)-ones-
dc.subject.keywordAuthoracylating agents-
dc.subject.keywordAuthorcoupling reactions-
dc.subject.keywordAuthorheterocycles-
dc.subject.keywordAuthormixed carbonic anhydrides-
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