Radical reaction of S-phenyl chlorothioformate with alkyl iodides: free radical-mediated carboxylation approach

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dc.contributor.authorKim, Sung Gakko
dc.contributor.authorJon, SYko
dc.date.accessioned2013-02-27T22:13:02Z-
dc.date.available2013-02-27T22:13:02Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1998-04-
dc.identifier.citationCHEMICAL COMMUNICATIONS, pp.815 - 816-
dc.identifier.issn1359-7345-
dc.identifier.urihttp://hdl.handle.net/10203/71136-
dc.description.abstractFree radical-mediated carboxylation is achieved by treatment of alkyl iodides with S-phenyl chlorothioformate and bis(tributyltin) with irradiation at 300 nm.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectSUBSTITUTION-
dc.subjectTHIOESTER-
dc.subjectKINETICS-
dc.titleRadical reaction of S-phenyl chlorothioformate with alkyl iodides: free radical-mediated carboxylation approach-
dc.typeArticle-
dc.identifier.wosid000073042400042-
dc.type.rimsART-
dc.citation.beginningpage815-
dc.citation.endingpage816-
dc.citation.publicationnameCHEMICAL COMMUNICATIONS-
dc.contributor.localauthorKim, Sung Gak-
dc.contributor.nonIdAuthorJon, SY-
dc.type.journalArticleArticle-
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CH-Journal Papers(저널논문)
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