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College of Engineering(공과대학)Dept. of Nuclear and Quantum Engineering(원자력및양자공학과)NE-Journal Papers(저널논문)

Radical cyclization of thio- and seleno-esters - An intramolecular acylation approach

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dc.contributor.authorKim, Sung Gakko
dc.contributor.authorJon, SYko
dc.date.accessioned2013-02-27T23:08:58Z-
dc.date.available2013-02-27T23:08:58Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1996-06-
dc.identifier.citationCHEMICAL COMMUNICATIONS, v.11, pp.1335 - 1336-
dc.identifier.issn1359-7345-
dc.identifier.urihttp://hdl.handle.net/10203/71379-
dc.description.abstractBoth thio- and seleno-esters are utilized as carbonyl equivalent radical accepters in radical cyclizations, where selenoesters are more efficient than thioesters due to the better leaving ability of the phenylseleno group.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectADDITION-REACTIONS-
dc.subjectMETHYLMALONYL-COA-
dc.subjectREARRANGEMENT-
dc.subjectMECHANISM-
dc.subjectKETONES-
dc.subjectMODEL-
dc.subjectTHIOESTER-
dc.subjectKINETICS-
dc.subjectCYANO-
dc.subjectACYL-
dc.titleRadical cyclization of thio- and seleno-esters - An intramolecular acylation approach-
dc.typeArticle-
dc.identifier.wosidA1996UR34700037-
dc.type.rimsART-
dc.citation.volume11-
dc.citation.beginningpage1335-
dc.citation.endingpage1336-
dc.citation.publicationnameCHEMICAL COMMUNICATIONS-
dc.contributor.localauthorKim, Sung Gak-
dc.contributor.nonIdAuthorJon, SY-
dc.type.journalArticleArticle-
dc.subject.keywordPlusADDITION-REACTIONS-
dc.subject.keywordPlusMETHYLMALONYL-COA-
dc.subject.keywordPlusREARRANGEMENT-
dc.subject.keywordPlusMECHANISM-
dc.subject.keywordPlusKETONES-
dc.subject.keywordPlusMODEL-
dc.subject.keywordPlusTHIOESTER-
dc.subject.keywordPlusKINETICS-
dc.subject.keywordPlusCYANO-
dc.subject.keywordPlusACYL-
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CH-Journal Papers(저널논문)
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