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dc.contributor.author이상기*
dc.date.accessioned2018-12-14T16:30:25Z-
dc.date.available2018-12-14T16:30:25Z-
dc.date.issued2018*
dc.identifier.issn2155-5435*
dc.identifier.otherOAK-22878*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/247581-
dc.description.abstractA straightforward route toward construction of a-quaternary chiral beta-lactam moiety via Rh(II)/Pd(0)-catalyzed stereoselective relay catalytic reaction is reported. This asymmetric dual relay catalysis involves Rh(II)-catalyzed enantioselective intramoluecular C-H insertions of alpha-diazoamides, and sequential Pd(0)-catalyzed diastereoselective intermolecular allylic alkylation. Under mild reaction conditions, a broad range of a-quaternary allylated chiral beta-lactams have been synthesized in high yields (up to 99%) with excellent stereoselectivities [up to diastereomeric ratio (dr) >99:1, up to 98% enantiomeric excess (ee)].*
dc.languageEnglish*
dc.publisherAMER CHEMICAL SOC*
dc.subjectbeta-lactam*
dc.subjectrhodium*
dc.subjectpalladium*
dc.subjectC-H insertion*
dc.subjectallylic alkylation*
dc.subjectasymmetric catalysis*
dc.titleAsymmetric Rh(II)/Pd(0) Relay Catalysis: Synthesis of alpha-Quaternary Chiral beta-Lactams through Enantioselective C-H Insertion/Diastereoselective Allylation of Diazoamides*
dc.typeArticle*
dc.relation.issue8*
dc.relation.volume8*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage7340*
dc.relation.lastpage7345*
dc.relation.journaltitleACS CATALYSIS*
dc.identifier.doi10.1021/acscatal.8b01687*
dc.identifier.wosidWOS:000441112400053*
dc.identifier.scopusid2-s2.0-85049316996*
dc.author.googleHuang, Liang-Zhu*
dc.author.googleXuan, Zi*
dc.author.googleJeon, Hyun Ji*
dc.author.googleDu, Zhen-Ting*
dc.author.googleKim, Ju Hyun*
dc.author.googleLee, Sang-gi*
dc.contributor.scopusid이상기(15082786300)*
dc.date.modifydate20240123104103*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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