A straightforward synthesis of 4-hydroxy-(E)-2-alkenoic esters mediated by SmI2

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dc.contributor.authorKwon, DWko
dc.contributor.authorCho, MSko
dc.contributor.authorKim, Yong Haeko
dc.date.accessioned2013-03-03T12:08:22Z-
dc.date.available2013-03-03T12:08:22Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2001-05-
dc.identifier.citationSYNLETT, pp.627 - 628-
dc.identifier.issn0936-5214-
dc.identifier.urihttp://hdl.handle.net/10203/78604-
dc.description.abstractCoupling reactions of ketones with propiolate esters in intermolecular manner by SmI2 gave 4-hydroxy-(E)-2-alkenoic esters in THF-t-BuOH at 0 degreesC in moderate to good yields.-
dc.languageEnglish-
dc.publisherGEORG THIEME VERLAG KG-
dc.subjectRADICAL CHAIN REACTIONS-
dc.subjectCARBON BOND FORMATION-
dc.subjectSAMARIUM(II) IODIDE-
dc.subjectORGANIC-SYNTHESIS-
dc.subjectGAMMA-HYDROXY-ALPHA,BETA-UNSATURATED ESTERS-
dc.subjectCYCLIZATION-
dc.subjectREDUCTIONS-
dc.subjectALDEHYDES-
dc.subjectDIIODIDE-
dc.subjectHALIDES-
dc.titleA straightforward synthesis of 4-hydroxy-(E)-2-alkenoic esters mediated by SmI2-
dc.typeArticle-
dc.identifier.wosid000168764600013-
dc.type.rimsART-
dc.citation.beginningpage627-
dc.citation.endingpage628-
dc.citation.publicationnameSYNLETT-
dc.contributor.nonIdAuthorKwon, DW-
dc.contributor.nonIdAuthorCho, MS-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorcoupling reaction-
dc.subject.keywordAuthorSmI2-
dc.subject.keywordAuthorintermolecular manner-
dc.subject.keywordAuthorpropiolate ester-
dc.subject.keywordAuthor4-hydroxy-(E)-2-alkenoic esters-
dc.subject.keywordPlusRADICAL CHAIN REACTIONS-
dc.subject.keywordPlusCARBON BOND FORMATION-
dc.subject.keywordPlusSAMARIUM(II) IODIDE-
dc.subject.keywordPlusORGANIC-SYNTHESIS-
dc.subject.keywordPlusGAMMA-HYDROXY-ALPHA,BETA-UNSATURATED ESTERS-
dc.subject.keywordPlusCYCLIZATION-
dc.subject.keywordPlusREDUCTIONS-
dc.subject.keywordPlusALDEHYDES-
dc.subject.keywordPlusDIIODIDE-
dc.subject.keywordPlusHALIDES-
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