Samarium(III) iodide complex catalyzed regioselective cleavage of epoxides to iodohydrins: Tandem epoxide opening-iodocyclization

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dc.contributor.authorKwon, DWko
dc.contributor.authorCho, MSko
dc.contributor.authorKim, Yong Haeko
dc.date.accessioned2013-03-03T12:34:14Z-
dc.date.available2013-03-03T12:34:14Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2003-06-
dc.identifier.citationSYNLETT, v.23, pp.959 - 962-
dc.identifier.issn0936-5214-
dc.identifier.urihttp://hdl.handle.net/10203/78693-
dc.description.abstractA novel tandem iodocyclization has been achieved by the regioselective ring-opening of epoxide and by the following intramolecular 1,4-cycloaddition of alpha,beta-unsaturated ester with catalytic amount of SMI2 and I-2 (1.2-2.5 equivalent) under mild and neutral reaction conditions.-
dc.languageEnglish-
dc.publisherGEORG THIEME VERLAG KG-
dc.subjectDIASTEREOSELECTIVE ALLYLATION-
dc.subjectTETRAHYDROFURANS-
dc.subjectREDUCTION-
dc.subjectALDEHYDES-
dc.subjectALKOXIDES-
dc.subjectALCOHOLS-
dc.subjectHALIDES-
dc.subjectKETONES-
dc.titleSamarium(III) iodide complex catalyzed regioselective cleavage of epoxides to iodohydrins: Tandem epoxide opening-iodocyclization-
dc.typeArticle-
dc.identifier.wosid000183377000008-
dc.type.rimsART-
dc.citation.volume23-
dc.citation.beginningpage959-
dc.citation.endingpage962-
dc.citation.publicationnameSYNLETT-
dc.contributor.nonIdAuthorKwon, DW-
dc.contributor.nonIdAuthorCho, MS-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorsamarium-
dc.subject.keywordAuthortandem reactions-
dc.subject.keywordAuthorring opening-
dc.subject.keywordAuthorcyclizations-
dc.subject.keywordAuthorregioselectivity-
dc.subject.keywordPlusDIASTEREOSELECTIVE ALLYLATION-
dc.subject.keywordPlusTETRAHYDROFURANS-
dc.subject.keywordPlusREDUCTION-
dc.subject.keywordPlusALDEHYDES-
dc.subject.keywordPlusALKOXIDES-
dc.subject.keywordPlusALCOHOLS-
dc.subject.keywordPlusHALIDES-
dc.subject.keywordPlusKETONES-
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