{"@context":{"@vocab":"https://cir.nii.ac.jp/schema/1.0/","rdfs":"http://www.w3.org/2000/01/rdf-schema#","dc":"http://purl.org/dc/elements/1.1/","dcterms":"http://purl.org/dc/terms/","foaf":"http://xmlns.com/foaf/0.1/","prism":"http://prismstandard.org/namespaces/basic/2.0/","cinii":"http://ci.nii.ac.jp/ns/1.0/","datacite":"https://schema.datacite.org/meta/kernel-4/","ndl":"http://ndl.go.jp/dcndl/terms/","jpcoar":"https://github.com/JPCOAR/schema/blob/master/2.0/"},"@id":"https://cir.nii.ac.jp/crid/1360004233149334784.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1021/acscatal.8b01675"}},{"identifier":{"@type":"URI","@value":"https://pubs.acs.org/doi/pdf/10.1021/acscatal.8b01675"}}],"resourceType":"学術雑誌論文(journal article)","dc:title":[{"@value":"Rhodium(I)-Catalyzed C8-Alkylation of 1-Naphthylamide Derivatives with Alkenes through a Bidentate Picolinamide Chelation System"}],"description":[{"notation":[{"@value":"The rhodium(I)-catalyzed C–H alkylation of 1-naphthylamide derivatives with alkenes at the C8-position using a picolinamide directing group is reported. Various alkenes including styrene derivatives, α,β-unsaturated carbonyl compounds, and even unactivated alkene could also be used as coupling partners. The reaction mechanism was investigated in kinetic studies, deuterium labeling studies, and control experiments. The reaction appears to proceed through a rhodium carbene intermediate, which is generated from an alkene."}]}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1380004233149334784","@type":"Researcher","foaf:name":[{"@value":"Supriya Rej"}],"jpcoar:affiliationName":[{"@value":"Department of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565-0871, Japan"}]},{"@id":"https://cir.nii.ac.jp/crid/1380004233149334656","@type":"Researcher","foaf:name":[{"@value":"Naoto Chatani"}],"jpcoar:affiliationName":[{"@value":"Department of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565-0871, Japan"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"21555435"},{"@type":"EISSN","@value":"21555435"}],"prism:publicationName":[{"@value":"ACS Catalysis"}],"dc:publisher":[{"@value":"American Chemical Society (ACS)"}],"prism:publicationDate":"2018-06-18","prism:volume":"8","prism:number":"7","prism:startingPage":"6699","prism:endingPage":"6706"},"reviewed":"false","url":[{"@id":"https://pubs.acs.org/doi/pdf/10.1021/acscatal.8b01675"}],"createdAt":"2018-06-18","modifiedAt":"2023-04-16","project":[{"@id":"https://cir.nii.ac.jp/crid/1040282256935953152","@type":"Project","projectIdentifier":[{"@type":"KAKEN","@value":"17H06091"},{"@type":"JGN","@value":"JP17H06091"},{"@type":"URI","@value":"https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-17H06091/"}],"notation":[{"@language":"ja","@value":"分子活性化を基軸とする次世代型触媒反応の開発"},{"@language":"en","@value":"Development of Next-Generation Transformation Invonving Molecular Activation as a Key Step"}]}],"relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1360002214424173440","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Catalytic Functionalization of C(sp<sup>2</sup>)H and 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