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Cited 29 time in webofscience Cited 33 time in scopus
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Enantioselective Total Synthesis of a Natural Iridoid

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dc.contributor.authorLee, Sujin-
dc.contributor.authorPaek, Seung-Mann-
dc.contributor.authorYun, Hwayoung-
dc.contributor.authorKim, Nam-Jung-
dc.contributor.authorSuh, Young-Ger-
dc.date.accessioned2022-12-27T03:03:23Z-
dc.date.available2022-12-27T03:03:23Z-
dc.date.issued2011-07-01-
dc.identifier.issn1523-7060-
dc.identifier.issn1523-7052-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/23658-
dc.description.abstractThe first total synthesis of 6-hydroxy-7-(hydroxymethyl)-4-methylenehexahydrocyclopenta[c]pyran-1(3H)-one has been accomplished. A key feature of the synthesis includes facile construction of the bicyclic lactone intermediate via intramolecular Pd(0)-catalyzed allylic alkylation and the efficient transformation of this intermediate into the iridoid skeleton employing silicon tethered radical cyclization.-
dc.format.extent4-
dc.language영어-
dc.language.isoENG-
dc.publisherAMER CHEMICAL SOC-
dc.titleEnantioselective Total Synthesis of a Natural Iridoid-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1021/ol201089f-
dc.identifier.scopusid2-s2.0-79959718779-
dc.identifier.wosid000291920800015-
dc.identifier.bibliographicCitationORGANIC LETTERS, v.13, no.13, pp 3344 - 3347-
dc.citation.titleORGANIC LETTERS-
dc.citation.volume13-
dc.citation.number13-
dc.citation.startPage3344-
dc.citation.endPage3347-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusASYMMETRIC TOTAL-SYNTHESIS-
dc.subject.keywordPlusRADICAL CYCLIZATION-
dc.subject.keywordPlusALPHA,BETA-UNSATURATED KETONES-
dc.subject.keywordPlusFORMAL SYNTHESIS-
dc.subject.keywordPlusREARRANGEMENT-
dc.subject.keywordPlusSECOIRIDOIDS-
dc.subject.keywordPlusVERSATILE-
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