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Pd-Catalyzed Asymmetric Hydrosilylation of Olefins with Planar Chiral Monophosphine Ligands

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dc.contributor.author한진욱-
dc.date.accessioned2021-08-04T01:39:16Z-
dc.date.available2021-08-04T01:39:16Z-
dc.date.issued2007-04-19-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/67863-
dc.description.abstractPlanar chiral (Arene)chromiumtricarbonyl monophosphine ligands were prepared by asymmetric ortho-lithiation as a key step to introduce planar chirality to arene ring. Palladium-catalyzed asymmetric hydrosilylation and oxidation of styrene derivatives and norbonadiene with these planar chiral monophosphine ligands gave the corresponding chiral diol in good yields.-
dc.titlePd-Catalyzed Asymmetric Hydrosilylation of Olefins with Planar Chiral Monophosphine Ligands-
dc.typeConference-
dc.citation.conferenceName대한화학회 제99회 총회 및 학술발표회-
dc.citation.conferencePlace서울 코엑스-
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서울 자연과학대학 > 서울 화학과 > 2. Conference Papers

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