{"@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/1363670320627447552.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1039/c7cc01755c"}},{"identifier":{"@type":"URI","@value":"http://pubs.rsc.org/en/content/articlepdf/2017/CC/C7CC01755C"}}],"dc:title":[{"@value":"The use of carboxylic acids as traceless directing groups for regioselective C–H bond functionalisation"}],"description":[{"type":"abstract","notation":[{"@value":"<p>This feature article focuses on the use of carboxylic acids as traceless directing groups and the application of this concept to achieve regiochemical control in organic chemistry.</p>"}]}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1383670320627447555","@type":"Researcher","foaf:name":[{"@value":"Marc Font"}],"jpcoar:affiliationName":[{"@value":"School of Chemistry"},{"@value":"University of Manchester"},{"@value":"Manchester"},{"@value":"UK"}]},{"@id":"https://cir.nii.ac.jp/crid/1383670320627447554","@type":"Researcher","foaf:name":[{"@value":"Jacob M. Quibell"}],"jpcoar:affiliationName":[{"@value":"School of Chemistry"},{"@value":"University of Manchester"},{"@value":"Manchester"},{"@value":"UK"}]},{"@id":"https://cir.nii.ac.jp/crid/1383670320627447552","@type":"Researcher","foaf:name":[{"@value":"Gregory J. P. Perry"}],"jpcoar:affiliationName":[{"@value":"School of Chemistry"},{"@value":"University of Manchester"},{"@value":"Manchester"},{"@value":"UK"}]},{"@id":"https://cir.nii.ac.jp/crid/1383670320627447553","@type":"Researcher","foaf:name":[{"@value":"Igor Larrosa"}],"jpcoar:affiliationName":[{"@value":"School of Chemistry"},{"@value":"University of Manchester"},{"@value":"Manchester"},{"@value":"UK"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"13597345"},{"@type":"EISSN","@value":"1364548X"}],"prism:publicationName":[{"@value":"Chemical Communications"}],"dc:publisher":[{"@value":"Royal Society of Chemistry (RSC)"}],"prism:publicationDate":"2017","prism:volume":"53","prism:number":"41","prism:startingPage":"5584","prism:endingPage":"5597"},"reviewed":"false","url":[{"@id":"http://pubs.rsc.org/en/content/articlepdf/2017/CC/C7CC01755C"}],"createdAt":"2017-04-28","modifiedAt":"2024-04-17","relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1050022476722772736","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Rhodium(III)-Catalyzed β-Arylation and -Alkenylation of α-Trifluoromethylacrylic Acid"}]},{"@id":"https://cir.nii.ac.jp/crid/1050022476722883712","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Iridium(III)-Catalyzed Dehydrogenative Coupling of Salicylic Acids with Alkynes: Synthesis of Highly Substituted 1-Naphthol Derivatives"},{"@value":"Iridium(III)‐Catalyzed Dehydrogenative Coupling of Salicylic Acids with Alkynes: Synthesis of Highly Substituted 1‐Naphthol Derivatives"}]},{"@id":"https://cir.nii.ac.jp/crid/1050299693922879488","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Rhodium-Catalyzed C4-Selective C-H Alkenylation of 2-Pyridones by Traceless Directing Group Strategy"}]},{"@id":"https://cir.nii.ac.jp/crid/1050861859453546368","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Rhodium-Catalyzed Annulative Coupling of Coumarin-3-Carboxylic Acids with Alkynes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360005516642874240","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Quantitative analysis of native reactive functional groups on carbon fiber surface: An electrochemical approach"}]},{"@id":"https://cir.nii.ac.jp/crid/1360017279829684480","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Palladium-Catalyzed Tandem Ester Dance/Decarbonylative Coupling Reactions"}]},{"@id":"https://cir.nii.ac.jp/crid/1360289145423247232","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Mechanistic Studies into Visible Light-Driven Carboxylation of Aryl Halides/Triflates by the Combined Use of Palladium and Photoredox Catalysts"}]},{"@id":"https://cir.nii.ac.jp/crid/1360290617390308352","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Rhodium(<scp>iii</scp>)-catalysed decarboxylative C–H functionalization of isoxazoles with alkenes and sulfoxonium ylides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360846639397644288","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Room Temperature Decarboxylative and Oxidative [2+2+2] Annulation of Benzoic Acids with Alkynes Catalyzed by an Electron‐Deficient Rhodium(III) Complex"}]},{"@id":"https://cir.nii.ac.jp/crid/1360853567669393536","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Strategic evolution in transition metal-catalyzed directed C–H bond activation and future directions"}]},{"@id":"https://cir.nii.ac.jp/crid/1390585946599833344","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"ja","@value":"遷移金属触媒を用いる芳香族カルボン酸類の位置選択的誘導体化"},{"@language":"en","@value":"Regioselective Functionalization of Aromatic Carboxylic Acids under Transition-Metal Catalysis"},{"@language":"ja-Kana","@value":"センイ キンゾク ショクバイ オ モチイル ホウコウゾク カルボン サンルイ ノ イチ センタクテキ ユウドウタイカ"}]},{"@id":"https://cir.nii.ac.jp/crid/2050307417127979136","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of indenones through rhodium(Ⅲ)-catalyzed [3+2] annulation utilizing a recyclable carbazolyl leaving group"}]},{"@id":"https://cir.nii.ac.jp/crid/2051714792009188864","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Pd-catalyzed C4-dearomative allylation of benzyl ammoniums with allyltributylstannane"}]}],"dataSourceIdentifier":[{"@type":"CROSSREF","@value":"10.1039/c7cc01755c"},{"@type":"CROSSREF","@value":"10.1002/adsc.201900919_references_DOI_6EFBldyJ84dLaAAJLmHNi2WgauJ"},{"@type":"CROSSREF","@value":"10.1016/j.apsusc.2019.07.185_references_DOI_6EFBldyJ84dLaAAJLmHNi2WgauJ"},{"@type":"CROSSREF","@value":"10.1246/bcsj.20210151_references_DOI_6EFBldyJ84dLaAAJLmHNi2WgauJ"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.2c01432_references_DOI_6EFBldyJ84dLaAAJLmHNi2WgauJ"},{"@type":"CROSSREF","@value":"10.1246/cl.200884_references_DOI_6EFBldyJ84dLaAAJLmHNi2WgauJ"},{"@type":"CROSSREF","@value":"10.1039/d0ob02027c_references_DOI_6EFBldyJ84dLaAAJLmHNi2WgauJ"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.1c00050_references_DOI_6EFBldyJ84dLaAAJLmHNi2WgauJ"},{"@type":"CROSSREF","@value":"10.1246/cl.190024_references_DOI_6EFBldyJ84dLaAAJLmHNi2WgauJ"},{"@type":"CROSSREF","@value":"10.1246/cl.230082_references_DOI_6EFBldyJ84dLaAAJLmHNi2WgauJ"},{"@type":"CROSSREF","@value":"10.1002/chem.201703928_references_DOI_6EFBldyJ84dLaAAJLmHNi2WgauJ"},{"@type":"CROSSREF","@value":"10.1246/cl.200216_references_DOI_6EFBldyJ84dLaAAJLmHNi2WgauJ"},{"@type":"CROSSREF","@value":"10.1016/j.ccr.2020.213683_references_DOI_6EFBldyJ84dLaAAJLmHNi2WgauJ"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.83.517_references_DOI_6EFBldyJ84dLaAAJLmHNi2WgauJ"}]}