Novel Reductive Cleavage Reaction of α-Halo Epoxides with SMI2: Synthesis of Cyclopropanols

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dc.contributor.authorPark, HSko
dc.contributor.authorChung, SHko
dc.contributor.authorKim, Yong Haeko
dc.date.accessioned2013-02-27T12:03:54Z-
dc.date.available2013-02-27T12:03:54Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1998-10-
dc.identifier.citationSYNLETT, no.10, pp.1073-
dc.identifier.issn0936-5214-
dc.identifier.urihttp://hdl.handle.net/10203/68461-
dc.description.abstractAryl substituted alpha-halo epoxide reacted with SmI2 to give the cyclopropanols in the presence of HMPA, while allyl alcohols were yielded in the absence of HMPA.-
dc.languageEnglish-
dc.publisherGEORG THIEME VERLAG KG-
dc.subjectALPHA,BETA-EPOXY KETONES-
dc.subjectSAMARIUM DIIODIDE-
dc.subjectCATALYZED-REARRANGEMENT-
dc.subjectORGANIC-SYNTHESIS-
dc.subjectRADICAL REACTIONS-
dc.subjectEFFICIENT ROUTE-
dc.subjectBOND-CLEAVAGE-
dc.subjectESTERS-
dc.subjectCYCLOPENTANOLS-
dc.subjectFRAGMENTATION-
dc.titleNovel Reductive Cleavage Reaction of α-Halo Epoxides with SMI2: Synthesis of Cyclopropanols-
dc.typeArticle-
dc.identifier.wosid000076768600016-
dc.type.rimsART-
dc.citation.issue10-
dc.citation.beginningpage1073-
dc.citation.publicationnameSYNLETT-
dc.contributor.nonIdAuthorPark, HS-
dc.contributor.nonIdAuthorChung, SH-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
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