Decarboxylative acylation approach of thiohydroxamate esters

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dc.contributor.authorKim, Sung Gakko
dc.contributor.authorLim, CJko
dc.contributor.authorSong, SEko
dc.contributor.authorKang, HYko
dc.date.accessioned2013-03-03T18:35:44Z-
dc.date.available2013-03-03T18:35:44Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2001-
dc.identifier.citationCHEMICAL COMMUNICATIONS, pp.1410 - 1411-
dc.identifier.issn1359-7345-
dc.identifier.urihttp://hdl.handle.net/10203/79923-
dc.description.abstractA decarboxylative acylation approach is achieved with thiohydroxamate ester 6, which is less reactive and more stable than Barton's ester 1.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectRADICAL CHAIN-REACTIONS-
dc.subjectCARBON-CARBON BONDS-
dc.subjectRATE CONSTANTS-
dc.subjectALKYL RADICALS-
dc.subjectINVENTION-
dc.subjectCHEMISTRY-
dc.subjectGENERATION-
dc.subjectCYCLIZATIONS-
dc.subjectPRECURSORS-
dc.subjectAMINYL-
dc.titleDecarboxylative acylation approach of thiohydroxamate esters-
dc.typeArticle-
dc.identifier.wosid000170014800042-
dc.type.rimsART-
dc.citation.beginningpage1410-
dc.citation.endingpage1411-
dc.citation.publicationnameCHEMICAL COMMUNICATIONS-
dc.identifier.doi10.1039/b104025c-
dc.contributor.localauthorKim, Sung Gak-
dc.contributor.nonIdAuthorLim, CJ-
dc.contributor.nonIdAuthorSong, SE-
dc.contributor.nonIdAuthorKang, HY-
dc.type.journalArticleArticle-
dc.subject.keywordPlusRADICAL CHAIN-REACTIONS-
dc.subject.keywordPlusCARBON-CARBON BONDS-
dc.subject.keywordPlusRATE CONSTANTS-
dc.subject.keywordPlusALKYL RADICALS-
dc.subject.keywordPlusINVENTION-
dc.subject.keywordPlusCHEMISTRY-
dc.subject.keywordPlusGENERATION-
dc.subject.keywordPlusCYCLIZATIONS-
dc.subject.keywordPlusPRECURSORS-
dc.subject.keywordPlusAMINYL-
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