Radical Cyanation of Alkyl Iodides with Diethylphosphoryl Cyanide

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dc.contributor.authorCho, Chang Hoko
dc.contributor.authorLee, Jin Youngko
dc.contributor.authorKim, Sung Gakko
dc.date.accessioned2013-03-09T06:29:06Z-
dc.date.available2013-03-09T06:29:06Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2009-01-
dc.identifier.citationSYNLETT, no.1, pp.81 - 84-
dc.identifier.issn0936-5214-
dc.identifier.urihttp://hdl.handle.net/10203/95595-
dc.description.abstractThe beta-elimination of an organophosphoryl group from an iminyl radical is observed for the first time. On the basis of this finding, radical cyanation of alkyl iodides is achieved by using diethylphosphoryl cyanide.-
dc.languageEnglish-
dc.publisherGEORG THIEME VERLAG KG-
dc.subjectINTRAMOLECULAR ACYLATION APPROACH-
dc.subjectCARBON BOND FORMATION-
dc.subjectBETA-ELIMINATION-
dc.subjectACYLPHOSPHONATE DERIVATIVES-
dc.subjectCYCLIZATION REACTIONS-
dc.subjectHYPOPHOSPHOROUS ACID-
dc.subjectPHOSPHONATE GROUP-
dc.subjectSULFONYL AZIDES-
dc.subjectNITROGEN BONDS-
dc.subjectTIN-
dc.titleRadical Cyanation of Alkyl Iodides with Diethylphosphoryl Cyanide-
dc.typeArticle-
dc.identifier.wosid000262526300018-
dc.type.rimsART-
dc.citation.issue1-
dc.citation.beginningpage81-
dc.citation.endingpage84-
dc.citation.publicationnameSYNLETT-
dc.identifier.doi10.1055/s-0028-1087385-
dc.contributor.localauthorKim, Sung Gak-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorradical-
dc.subject.keywordAuthorcyanide-
dc.subject.keywordAuthorelimination-
dc.subject.keywordAuthoralkyl halides-
dc.subject.keywordPlusINTRAMOLECULAR ACYLATION APPROACH-
dc.subject.keywordPlusCARBON BOND FORMATION-
dc.subject.keywordPlusBETA-ELIMINATION-
dc.subject.keywordPlusACYLPHOSPHONATE DERIVATIVES-
dc.subject.keywordPlusCYCLIZATION REACTIONS-
dc.subject.keywordPlusHYPOPHOSPHOROUS ACID-
dc.subject.keywordPlusPHOSPHONATE GROUP-
dc.subject.keywordPlusSULFONYL AZIDES-
dc.subject.keywordPlusNITROGEN BONDS-
dc.subject.keywordPlusTIN-
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