Preparation of cycloalkanone oxime ethers via a free radical acylation approach

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dc.contributor.authorKim, Sung Gakko
dc.contributor.authorKim, Nko
dc.contributor.authorYoon, JYko
dc.contributor.authorOh, DHko
dc.date.accessioned2013-02-27T19:44:05Z-
dc.date.available2013-02-27T19:44:05Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2000-08-
dc.identifier.citationSYNLETT, pp.1148 - 1150-
dc.identifier.issn0936-5214-
dc.identifier.urihttp://hdl.handle.net/10203/70457-
dc.description.abstractRadical-mediated annulation approaches for the formation of cycloalkanone oxime ethers are described. Based on radical acylation approaches, alpha-functionalized cycloalkanone oxime ethers, 1,3- and 1,4-cyclohexanedione oxime ethers are prepared.-
dc.languageEnglish-
dc.publisherGEORG THIEME VERLAG-
dc.subjectCARBON BOND FORMATION-
dc.subjectALPHA-AMINO-ACIDS-
dc.titlePreparation of cycloalkanone oxime ethers via a free radical acylation approach-
dc.typeArticle-
dc.identifier.wosid000088896800017-
dc.type.rimsART-
dc.citation.beginningpage1148-
dc.citation.endingpage1150-
dc.citation.publicationnameSYNLETT-
dc.contributor.localauthorKim, Sung Gak-
dc.contributor.nonIdAuthorKim, N-
dc.contributor.nonIdAuthorYoon, JY-
dc.contributor.nonIdAuthorOh, DH-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorradical annulation-
dc.subject.keywordAuthorradical acylation-
dc.subject.keywordAuthorcycloalkanone oxime ether-
dc.subject.keywordAuthorsulfonyl oxime ether-
dc.subject.keywordPlusCARBON BOND FORMATION-
dc.subject.keywordPlusALPHA-AMINO-ACIDS-
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