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dc.contributor.authorShin, Chul-
dc.contributor.authorOh, Youna-
dc.contributor.authorCha, Joo Hwan-
dc.contributor.authorPae, Ae Nim-
dc.contributor.authorChoo, Hyunah-
dc.contributor.authorCho, Yong Seo-
dc.date.accessioned2024-01-21T01:06:33Z-
dc.date.available2024-01-21T01:06:33Z-
dc.date.created2021-09-05-
dc.date.issued2007-03-05-
dc.identifier.issn0040-4020-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/134544-
dc.description.abstractPrins-type cyclization followed by palladium-catalyzed cyclization provided sterically congested bi- or tricyclic tetrahydrofurans, which are very stereoselective as well. cis-2,5-Disubstituted tetrahydrofurans obtained from Prins-type cyclization have an allenyl group and a functional group such as alcohol, carboxylic acid, and aryl halide. The tetrahydrofurans bearing an allene group underwent palladium-catalyzed cyclization to give sterically congested bi- or tricyclic tetrahydrofurans. (c) 2007 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectPRINS-TYPE CYCLIZATION-
dc.subjectSAKURAI ISMS REACTION-
dc.subjectDIASTEREOSELECTIVE SYNTHESIS-
dc.subjectENANTIOSELECTIVE SYNTHESIS-
dc.subjectTHERMAL BENZANNULATION-
dc.subjectTETRAHYDROPYRANS-
dc.subjectMONOCERIN-
dc.subjectCONSTRUCTION-
dc.subjectDERIVATIVES-
dc.subjectANTIFUNGAL-
dc.titleSynthesis of sterically congested bicyclic tetrahydrofurans via Pd-catalyzed cyclization-
dc.typeArticle-
dc.identifier.doi10.1016/j.tet.2006.12.080-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTETRAHEDRON, v.63, no.10, pp.2182 - 2190-
dc.citation.titleTETRAHEDRON-
dc.citation.volume63-
dc.citation.number10-
dc.citation.startPage2182-
dc.citation.endPage2190-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000244536500009-
dc.identifier.scopusid2-s2.0-33846618144-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusPRINS-TYPE CYCLIZATION-
dc.subject.keywordPlusSAKURAI ISMS REACTION-
dc.subject.keywordPlusDIASTEREOSELECTIVE SYNTHESIS-
dc.subject.keywordPlusENANTIOSELECTIVE SYNTHESIS-
dc.subject.keywordPlusTHERMAL BENZANNULATION-
dc.subject.keywordPlusTETRAHYDROPYRANS-
dc.subject.keywordPlusMONOCERIN-
dc.subject.keywordPlusCONSTRUCTION-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordPlusANTIFUNGAL-
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