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Highly diastereoselective type-I IMDA reaction forming medium-sized macrolactones

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dc.contributor.authorShin, Jeong-Taek-
dc.contributor.authorHong, Sung-Cho-
dc.contributor.authorShin, Seunghoon-
dc.contributor.authorCho, Cheon-Gyu-
dc.date.accessioned2022-12-21T10:58:34Z-
dc.date.available2022-12-21T10:58:34Z-
dc.date.created2022-09-16-
dc.date.issued2006-07-
dc.identifier.issn1523-7060-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/181262-
dc.description.abstractIntramolecular Diels-Alder (IMDA) reactions of 2-pyrones containing an alkyne tether occur with remarkably high diastereofacial selectivity to provide medium-sized macrolactones. Because of the strain in the alkyne-tethered macrocyclic system, a single methyl group in the tether provides sufficient conformational bias to generate medium-sized macrocycles with unusually high selectivity.-
dc.language영어-
dc.language.isoen-
dc.publisherAMER CHEMICAL SOC-
dc.titleHighly diastereoselective type-I IMDA reaction forming medium-sized macrolactones-
dc.typeArticle-
dc.contributor.affiliatedAuthorShin, Seunghoon-
dc.contributor.affiliatedAuthorCho, Cheon-Gyu-
dc.identifier.doi10.1021/ol061198g-
dc.identifier.scopusid2-s2.0-33746889017-
dc.identifier.wosid000239001500046-
dc.identifier.bibliographicCitationORGANIC LETTERS, v.8, no.15, pp.3339 - 3341-
dc.relation.isPartOfORGANIC LETTERS-
dc.citation.titleORGANIC LETTERS-
dc.citation.volume8-
dc.citation.number15-
dc.citation.startPage3339-
dc.citation.endPage3341-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusDIELS-ALDER CYCLOADDITIONS-
dc.subject.keywordPlusSTILLE COUPLING REACTIONS-
dc.subject.keywordPlusASYMMETRIC-SYNTHESIS-
dc.subject.keywordPlus3,5-DIBROMO-2-PYRONE-
dc.subject.keywordPlusPATHWAYS-
dc.subject.keywordPlusACCESS-
dc.subject.keywordPlusARYL-
dc.identifier.urlhttps://pubs.acs.org/doi/10.1021/ol061198g-
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