DSpace at KISTKIST Article2004

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dc.contributor.authorKeum, GC-
dc.contributor.authorKang, SB-
dc.contributor.authorKim, Y-
dc.contributor.authorLee, E-
dc.date.accessioned2024-01-21T06:45:27Z-
dc.date.available2024-01-21T06:45:27Z-
dc.date.created2021-09-02-
dc.date.issued2004-06-10-
dc.identifier.issn1523-7060-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/137490-
dc.description.abstractTetrahydrofuranyl allyl carbinols may be prepared stereoselectively via radical cyclization of beta-alkoxyvinyl sulfoxides, Pummerer rearrangement, and reaction with allylstannane.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.titleStereoselection in radical cyclization of beta-alkoxyvinyl sulfoxides: Synthesis of tetrahydrofuranyl allyl carbinols-
dc.typeArticle-
dc.identifier.doi10.1021/ol049676f-
dc.description.journalClass1-
dc.identifier.bibliographicCitationORGANIC LETTERS, v.6, no.12, pp.1895 - 1897-
dc.citation.titleORGANIC LETTERS-
dc.citation.volume6-
dc.citation.number12-
dc.citation.startPage1895-
dc.citation.endPage1897-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000221868300004-
dc.identifier.scopusid2-s2.0-3042833041-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordAuthortetrahydrofuranyl-
dc.subject.keywordAuthorcarbinol-
dc.subject.keywordAuthorpummerer rearrengement-
dc.subject.keywordAuthorallylstannane-
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