{"@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/1362262944501632384.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1021/ja401022x"}},{"identifier":{"@type":"URI","@value":"https://pubs.acs.org/doi/pdf/10.1021/ja401022x"}}],"dc:title":[{"@value":"Catalytic Hydrotrifluoromethylation of Unactivated Alkenes"}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1382262944501632385","@type":"Researcher","foaf:name":[{"@value":"Satoshi Mizuta"}],"jpcoar:affiliationName":[{"@value":"Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford OX1\r3TA, United Kingdom"}]},{"@id":"https://cir.nii.ac.jp/crid/1382262944501632390","@type":"Researcher","foaf:name":[{"@value":"Stefan Verhoog"}],"jpcoar:affiliationName":[{"@value":"Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford OX1\r3TA, United Kingdom"}]},{"@id":"https://cir.nii.ac.jp/crid/1382262944501632389","@type":"Researcher","foaf:name":[{"@value":"Keary M. Engle"}],"jpcoar:affiliationName":[{"@value":"Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford OX1\r3TA, United Kingdom"}]},{"@id":"https://cir.nii.ac.jp/crid/1382262944501632384","@type":"Researcher","foaf:name":[{"@value":"Tanatorn Khotavivattana"}],"jpcoar:affiliationName":[{"@value":"Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford OX1\r3TA, United Kingdom"}]},{"@id":"https://cir.nii.ac.jp/crid/1382262944501632386","@type":"Researcher","foaf:name":[{"@value":"Miriam O’Duill"}],"jpcoar:affiliationName":[{"@value":"Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford OX1\r3TA, United Kingdom"}]},{"@id":"https://cir.nii.ac.jp/crid/1382262944501632257","@type":"Researcher","foaf:name":[{"@value":"Katherine Wheelhouse"}],"jpcoar:affiliationName":[{"@value":"Medicines Discovery & Development, GlaxoSmithKline R&D, Gunnels Wood Road, Stevenage, Hertfordshire SG1 2NY, United Kingdom"}]},{"@id":"https://cir.nii.ac.jp/crid/1382262944501632388","@type":"Researcher","foaf:name":[{"@value":"Gerasimos Rassias"}],"jpcoar:affiliationName":[{"@value":"Medicines Discovery & Development, GlaxoSmithKline R&D, Gunnels Wood Road, Stevenage, Hertfordshire SG1 2NY, United Kingdom"}]},{"@id":"https://cir.nii.ac.jp/crid/1382262944501632387","@type":"Researcher","foaf:name":[{"@value":"Maurice Médebielle"}],"jpcoar:affiliationName":[{"@value":"Université Claude Bernard Lyon I, ICBMS UMR CNRS − UCBL\r− INSA 5246, Equipe “Synthèse de Molécules\rd’Intérêt Thérapeutique (SMITH)”\r43 Boulevard du 11 Novembre 1918, Villeurbanne 69622, France"}]},{"@id":"https://cir.nii.ac.jp/crid/1382262944501632256","@type":"Researcher","foaf:name":[{"@value":"Véronique Gouverneur"}],"jpcoar:affiliationName":[{"@value":"Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford OX1\r3TA, United Kingdom"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"00027863"},{"@type":"EISSN","@value":"15205126"}],"prism:publicationName":[{"@value":"Journal of the American Chemical Society"}],"dc:publisher":[{"@value":"American Chemical Society (ACS)"}],"prism:publicationDate":"2013-02-07","prism:volume":"135","prism:number":"7","prism:startingPage":"2505","prism:endingPage":"2508"},"reviewed":"false","url":[{"@id":"https://pubs.acs.org/doi/pdf/10.1021/ja401022x"}],"createdAt":"2013-02-01","modifiedAt":"2023-04-18","relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1360002214424580096","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Combining Photoredox‐Catalyzed Trifluoromethylation and Oxidation with DMSO: Facile Synthesis of α‐Trifluoromethylated Ketones from Aromatic Alkenes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360002215859612160","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"New Horizons of Photocatalytic Fluoromethylative Difunctionalization of Alkenes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004233130714624","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Aqueous-Medium Carbon–Carbon Bond-Forming Radical Reactions Catalyzed by Excited Rhodamine B as a Metal-Free Organic Dye under Visible Light Irradiation"}]},{"@id":"https://cir.nii.ac.jp/crid/1360282588974445824","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Carbon radical addition–cyclization reaction induced by ruthenium-photocatalyst under visible light irradiation"}]},{"@id":"https://cir.nii.ac.jp/crid/1360283691580195712","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Fine Design of Photoredox Systems for Catalytic Fluoromethylation of Carbon–Carbon Multiple Bonds"}]},{"@id":"https://cir.nii.ac.jp/crid/1360283691585387648","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Photoredox-Catalyzed Hydrodifluoroalkylation of Alkenes Using Difluorohaloalkyl Compounds and a Hantzsch Ester"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285704923737856","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Photoredox‐Catalyzed Alkenylation of Benzylsulfonium Salts"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285704971216512","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Free‐Radical Carbo‐Alkenylation of Olefins: Scope, Limitations and Mechanistic Insights"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285708118475520","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"<i>Anti</i>-Diastereoselective Synthesis of CF<sub>3</sub>-Containing Spirooxazolines and Spirooxazines via Regiospecific Trifluoromethylative Spirocyclization by Photoredox Catalysis"}]},{"@id":"https://cir.nii.ac.jp/crid/1360286992987191936","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"C–H γ,γ,γ-Trifluoroalkylation of Quinolines via Visible-Light-Induced Sequential Radical Additions"}]},{"@id":"https://cir.nii.ac.jp/crid/1360564063938541184","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Direct C–H trifluoromethylation of di- and trisubstituted alkenes by photoredox catalysis"}]},{"@id":"https://cir.nii.ac.jp/crid/1360565164378487680","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Photoredox‐Catalyzed Stereoselective Conversion of Alkynes into Tetrasubstituted Trifluoromethylated Alkenes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360565166635607424","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Highly Regio- and Diastereoselective Synthesis of CF<sub>3</sub>-Substituted Lactones <i>via</i> Photoredox-Catalyzed Carbolactonization of Alkenoic Acids"}]},{"@id":"https://cir.nii.ac.jp/crid/1360565166840633600","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Mechanisms and applications of cyclometalated Pt(<scp>ii</scp>) complexes in photoredox catalytic trifluoromethylation"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567180198747136","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Trifluoroethoxy‐Coated Subphthalocyanine affects Trifluoromethylation of Alkenes and Alkynes even under Low‐Energy Red‐Light Irradiation"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567183203064448","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Cobalt-Catalyzed Hydrofluorination of Unactivated Olefins: A Radical Approach of Fluorine Transfer"}]},{"@id":"https://cir.nii.ac.jp/crid/1360580230578633728","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of Organofluorine Compounds"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848654856539392","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of Elongated Esters from Alkenes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848658539286016","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"A versatile strategy for difunctionalization of carbon–carbon multiple bonds by photoredox catalysis"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848658737283712","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"18 Photocatalytic Introduction of Fluorinated Groups"}]},{"@id":"https://cir.nii.ac.jp/crid/1360861705587639552","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Evolution and Future of Hetero‐ and Hydro‐Trifluoromethylations of Unsaturated C−C Bonds"}]},{"@id":"https://cir.nii.ac.jp/crid/1390001204142494208","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Development of Shelf-Stable Reagents for Fluoro-Functionalization Reactions"},{"@value":"Award Accounts : The Chemical Society of Japan Award for Creative Work for 2014 : Development of Shelf-Stable Reagents for Fluoro-Functionalization Reactions"}]},{"@id":"https://cir.nii.ac.jp/crid/1390001205341159680","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Organometallic Photocatalysis Promoted by Visible Light (Sunlight): Photo-redox Catalysis and Difunctional Dinuclear Catalyst System"},{"@language":"ja","@value":"可視光（太陽光）促進有機金属触媒反応：フォトレドックス触媒と機能分担型二核錯体触媒系"},{"@language":"ja-Kana","@value":"カシコウ(タイヨウコウ)ソクシン ユウキ キンゾク ショクバイ ハンノウ : フォトレドックス ショクバイ ト キノウ ブンタンガタ ニカク サクタイ ショクバイケイ"}]},{"@id":"https://cir.nii.ac.jp/crid/1390282680316308480","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"ja","@value":"コバルト触媒を利用したオレフィンへのMarkovnikov選択的付加反応における新展開"},{"@language":"en","@value":"Markovnikov-selective Addition Reaction to Olefins Using Cobalt Complex"},{"@language":"ja-Kana","@value":"コバルト ショクバイ オ リヨウ シタ オレフィン エ ノ Markovnikov センタクテキ フカ ハンノウ ニ オケル シン テンカイ"}]},{"@id":"https://cir.nii.ac.jp/crid/2050588892096788096","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Fluoroalkylation methods for synthesizing versatile building blocks"}]}],"dataSourceIdentifier":[{"@type":"CROSSREF","@value":"10.1021/ja401022x"},{"@type":"CROSSREF","@value":"10.1002/anie.201403590_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.1021/acs.accounts.6b00268_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.72.538_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.1246/bcsj.20190080_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.1002/asia.201801732_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.1002/chem.201605043_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.1021/acs.joc.6b01102_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.3762/bjoc.10.108_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.1002/anie.201505550_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.1039/c4sc02537g_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.1002/open.201600172_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.1016/j.chempr.2017.11.004_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.1246/bcsj.20160223_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.1007/978-3-030-63713-2_53_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.1002/anie.201809115_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.1039/c6qo00139d_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.1021/ol402696h_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.1002/adsc.202201268_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.1055/sos-sd-229-00316_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.1016/j.tet.2014.12.068_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.5b01694_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.73.788_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.1021/ol403500y_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.1021/acs.joc.7b00609_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.9b01015_references_DOI_CYEZBrauKRhKon1VmKZMRbBeK8O"}]}