Copper-Catalyzed Regiodivergent Internal Allylic Alkylations

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dc.contributor.authorManna, Madhu Sudanko
dc.contributor.authorYoo, Seok Yeolko
dc.contributor.authorSharique, Mohammedko
dc.contributor.authorChoi, Hyojuko
dc.contributor.authorPudasaini, Bimalko
dc.contributor.authorBaik, Mu-Hyunko
dc.contributor.authorTambar, Uttam K.ko
dc.date.accessioned2023-09-19T09:03:01Z-
dc.date.available2023-09-19T09:03:01Z-
dc.date.created2023-09-19-
dc.date.created2023-09-19-
dc.date.created2023-09-19-
dc.date.issued2023-08-
dc.identifier.citationANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.62, no.35-
dc.identifier.issn1433-7851-
dc.identifier.urihttp://hdl.handle.net/10203/312758-
dc.description.abstractWe report a copper-catalyzed, regioselective, and stereospecific alkylation of unbiased internal allylic carbonates with functionalized alkyl and aryl Grignard reagents. The reactions exhibit high stereospecificity and regioselectivity for either S(N)2 or S(N)2 ' products under two sets of copper-catalyzed conditions, which enables the preparation of a broad range of products with E-alkene selectivity. Density functional theory calculations reveal the origins of the regioselectivity based on the different behaviors of homo- and heterocuprates.-
dc.languageEnglish-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.titleCopper-Catalyzed Regiodivergent Internal Allylic Alkylations-
dc.typeArticle-
dc.identifier.wosid001053110800017-
dc.identifier.scopusid2-s2.0-85164945554-
dc.type.rimsART-
dc.citation.volume62-
dc.citation.issue35-
dc.citation.publicationnameANGEWANDTE CHEMIE-INTERNATIONAL EDITION-
dc.identifier.doi10.1002/anie.202304848-
dc.contributor.localauthorBaik, Mu-Hyun-
dc.contributor.nonIdAuthorManna, Madhu Sudan-
dc.contributor.nonIdAuthorSharique, Mohammed-
dc.contributor.nonIdAuthorPudasaini, Bimal-
dc.contributor.nonIdAuthorTambar, Uttam K.-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorAllylic Alkylation-
dc.subject.keywordAuthorCopper-
dc.subject.keywordAuthorDensity Functional Calculations-
dc.subject.keywordAuthorRegioselecitvity-
dc.subject.keywordAuthorStereospecific-
dc.subject.keywordPlusCONJUGATE ADDITION-
dc.subject.keywordPlusPHOSPHOROTHIOATE ESTERS-
dc.subject.keywordPlusORGANOCUPRATE CLUSTERS-
dc.subject.keywordPlusGRIGNARD-REAGENTS-
dc.subject.keywordPlusENERGIES-
dc.subject.keywordPlusREACTIVITIES-
dc.subject.keywordPlusSUBSTITUTION-
dc.subject.keywordPlusCARBONATES-
dc.subject.keywordPlusMECHANISM-
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