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Copper(i)/DM-SEGPHOS-catalyzed enantio- and diastereoselective conjugate boration to alpha-alkylidene-gamma-lactams

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dc.contributor.authorGeorge, Jimit-
dc.contributor.authorKim, Hun Young-
dc.contributor.authorOh, Kyungsoo-
dc.date.available2020-04-10T02:20:57Z-
dc.date.issued2020-02-21-
dc.identifier.issn2052-4129-
dc.identifier.issn2052-4129-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/38169-
dc.description.abstractA combination of CuCl and DM-SEGPHOS catalyst system has allowed the development of highly enantioselective and diastereoselective conjugate addition of bis(pinacolato)diboron to alpha-alkylidene-gamma-lactams. The key structural feature of conjugate acceptors, alpha-alkylidene-gamma-lactams, was identified as the carbamate group such as N-Boc and N-Cbz, where the typical low reactivity and stereoselectivity issues associated with alpha,beta-unsaturated lactams as conjugate acceptors were resolved.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleCopper(i)/DM-SEGPHOS-catalyzed enantio- and diastereoselective conjugate boration to alpha-alkylidene-gamma-lactams-
dc.typeArticle-
dc.identifier.doi10.1039/c9qo01504c-
dc.identifier.bibliographicCitationORGANIC CHEMISTRY FRONTIERS, v.7, no.4, pp 709 - 714-
dc.description.isOpenAccessN-
dc.identifier.wosid000515578100009-
dc.identifier.scopusid2-s2.0-85079828934-
dc.citation.endPage714-
dc.citation.number4-
dc.citation.startPage709-
dc.citation.titleORGANIC CHEMISTRY FRONTIERS-
dc.citation.volume7-
dc.type.docTypeArticle-
dc.publisher.location영국-
dc.subject.keywordPlusALPHA,BETA-UNSATURATED CARBONYL-COMPOUNDS-
dc.subject.keywordPlusENANTIOSELECTIVE BETA-BORATION-
dc.subject.keywordPlusCATALYTIC ASYMMETRIC-SYNTHESIS-
dc.subject.keywordPlusESTERS-
dc.subject.keywordPlusADDITIONS-
dc.subject.keywordPlusHYDROGENATION-
dc.subject.keywordPlusHYDROBORATION-
dc.subject.keywordPlusBORYLATION-
dc.subject.keywordPlusTERTIARY-
dc.subject.keywordPlusBOND-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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