{"@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/1360002214425440896.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1002/anie.201604127"}},{"identifier":{"@type":"URI","@value":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fanie.201604127"}},{"identifier":{"@type":"URI","@value":"https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201604127"}}],"resourceType":"学術雑誌論文(journal article)","dc:title":[{"@value":"Perfluoroalkylation of Unactivated Alkenes with Acid Anhydrides as the Perfluoroalkyl Source"}],"description":[{"type":"abstract","notation":[{"@value":"<jats:title>Abstract</jats:title><jats:p>An efficient perfluoroalkylation of unactivated alkenes with perfluoro acid anhydrides was developed. Copper salts play a crucial role as a catalyst to achieve allylic perfluoroalkylation with the in situ generated bis(perfluoroacyl) peroxides. Furthermore, carboperfluoroalkylation of alkene bearing an aromatic ring at an appropriate position on the carbon side chain was found to proceed under metal‐free conditions to afford carbocycles or heterocycles bearing a perfluoroalkyl group. This method, which makes use of readily available perfluoroalkyl sources, offers a convenient and powerful tool for introducing a perfluoroalkyl group onto an sp<jats:sup>3</jats:sup> carbon to construct synthetically useful skeletons.</jats:p>"}]}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1420282801199834752","@type":"Researcher","personIdentifier":[{"@type":"KAKEN_RESEARCHERS","@value":"60732956"},{"@type":"NRID","@value":"1000060732956"},{"@type":"ORCID","@value":"0000-0002-7422-837X"},{"@type":"NRID","@value":"9000305636313"},{"@type":"NRID","@value":"9000019141566"},{"@type":"NRID","@value":"9000248231007"},{"@type":"NRID","@value":"9000399851872"},{"@type":"NRID","@value":"9000403282467"},{"@type":"NRID","@value":"9000018773651"},{"@type":"NRID","@value":"9000303993398"},{"@type":"NRID","@value":"9000239229810"},{"@type":"RESEARCHMAP","@value":"https://researchmap.jp/skawamura"}],"foaf:name":[{"@value":"Shintaro Kawamura"}],"jpcoar:affiliationName":[{"@value":"Synthetic Organic Chemistry Laboratory RIKEN  2-1 Hirosawa, Wako Saitama 351-0198 Japan"},{"@value":"RIKEN Center for Sustainable Resource Science  2-1 Hirosawa, Wako Saitama 351-0198 Japan"}]},{"@id":"https://cir.nii.ac.jp/crid/1380566392500403840","@type":"Researcher","foaf:name":[{"@value":"Mikiko Sodeoka"}],"jpcoar:affiliationName":[{"@value":"Synthetic Organic Chemistry Laboratory RIKEN  2-1 Hirosawa, Wako Saitama 351-0198 Japan"},{"@value":"RIKEN Center for Sustainable Resource Science  2-1 Hirosawa, Wako Saitama 351-0198 Japan"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"14337851"},{"@type":"EISSN","@value":"15213773"}],"prism:publicationName":[{"@value":"Angewandte Chemie International Edition"}],"dc:publisher":[{"@value":"Wiley"}],"prism:publicationDate":"2016-06-02","prism:volume":"55","prism:number":"30","prism:startingPage":"8740","prism:endingPage":"8743"},"reviewed":"false","dc:rights":["http://onlinelibrary.wiley.com/termsAndConditions#vor"],"url":[{"@id":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fanie.201604127"},{"@id":"https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201604127"}],"createdAt":"2016-06-02","modifiedAt":"2023-09-16","project":[{"@id":"https://cir.nii.ac.jp/crid/1040282256839516416","@type":"Project","projectIdentifier":[{"@type":"KAKEN","@value":"15K17860"},{"@type":"JGN","@value":"JP15K17860"},{"@type":"URI","@value":"https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-15K17860/"}],"notation":[{"@language":"ja","@value":"新規キラル有機ヨウ素触媒を用いるトリフルオロメチル化反応の開発"},{"@language":"en","@value":"Development of trifluoromethylation reaction by using a novel chiral hypervalent iodine catalyst"}]}],"relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1360004233131099904","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"<i>N</i>-Heterocycle-Forming Amino/Carboperfluoroalkylations of Aminoalkenes by Using Perfluoro Acid Anhydrides: Mechanistic Studies and Applications Directed Toward Perfluoroalkylated Compound Libraries"}]},{"@id":"https://cir.nii.ac.jp/crid/1360011144080355712","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Copper‐Catalyzed Trifluoromethylation‐Initiated Radical 1,2‐Aryl Migration in α,α‐Diaryl Allylic Alcohols"}]},{"@id":"https://cir.nii.ac.jp/crid/1360021390581574400","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Intramolecular Cyclization of N-Propargylic Amides without Transition-Metal Catalysis for Synthesis of Fluoroalkylated Oxazoles: Using Carboxylic Acid Anhydrides as the Fluoroalkyl Source"}]},{"@id":"https://cir.nii.ac.jp/crid/1360025430643102976","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Ligand‐Controlled Copper‐Catalyzed Halo‐Halodifluoromethylation of Alkenes and Alkynes Using Fluorinated Carboxylic Anhydrides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360283689400816768","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Alkene Trifluoromethylation Coupled with CC Bond Formation: Construction of Trifluoromethylated Carbocycles and Heterocycles"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292617907821440","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Fluorine in medicinal chemistry"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292618874038528","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Trifluoromethylation of aromatic compounds with bis(trifluoroacetyl) peroxide"}]},{"@id":"https://cir.nii.ac.jp/crid/1360302865542060928","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Catalytic Difluoromethylation of Alkenes with Difluoroacetic Anhydride: Reactivity of Fluorinated Diacyl Peroxides and Radicals"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567182230026752","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of CF3-containing oxazolines via trifluoromethylation of allylamides with Togni reagent in the presence of alkali metal iodides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574093676495488","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Concise synthesis of oxindole derivatives bearing a 3-trifluoroethyl group: Copper-catalyzed trifluoromethylation of acryloanilides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574093696857088","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Aminotrifluoromethylation of Olefins via Cyclic Amine Formation: Mechanistic Study and Application to Synthesis of Trifluoromethylated Pyrrolidines"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574094182077952","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Trifluoromethylation of Alkenes with Concomitant Introduction of Additional Functional Groups"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574094359538560","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Copper‐Catalyzed Trifluoromethylation of Allylsilanes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574095720473600","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Fluorinated Peroxides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848657457467008","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Oxytrifluoromethylation of multiple bonds using copper catalyst under mild conditions"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855568693018880","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Fluorine in Pharmaceutical and Medicinal Chemistry"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855569456998016","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Oxy-trifluoromethylation of alkenes and its application to the synthesis of β-trifluoromethylstyrene derivatives"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855569673672576","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Copper-Catalyzed One-Pot Trifluoromethylation/Aryl Migration/Desulfonylation and C(sp<sup>2</sup>)–N Bond Formation of Conjugated Tosyl Amides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855569732753536","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Free-radical selective functionalization of 1,4-naphthoquinones by perfluorodiacyl peroxides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855569800771968","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Copper-Catalyzed Oxidative Trifluoromethylation of Terminal Alkenes Using Nucleophilic CF<sub>3</sub>SiMe<sub>3</sub>: Efficient C(sp<sup>3</sup>)–CF<sub>3</sub> Bond Formation"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855570370332288","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Copper-Catalyzed Intermolecular Cyanotrifluoromethylation of Alkenes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855570468414720","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Metal‐Free Trifluoromethylation and Arylation of Alkenes: Domino Synthesis of Oxindole Derivatives"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855570971462400","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Copper-Catalyzed Trifluoromethylation of Terminal Alkenes through Allylic C–H Bond Activation"}]},{"@id":"https://cir.nii.ac.jp/crid/1360857593807747328","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"1,2-Bis-perfluoroalkylations of alkenes and alkynes with perfluorocarboxylic anhydrides<i>via</i>the formation of perfluoroalkylcopper intermediates"}]},{"@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/1360865815494096896","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Understanding and Controlling Fluorinated Diacyl Peroxides and Fluoroalkyl Radicals in Alkene Fluoroalkylations"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137043551285248","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The Many Roles for Fluorine in Medicinal Chemistry"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137043996795520","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Copper‐Catalyzed Trifluoromethylation of Unactivated Olefins"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418518742683648","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Perfluoroalkylations of nitrogen-containing heteroaromatic compounds with bis(perfluoroalkanoyl) peroxides"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418520189420032","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Copper‐Catalyzed Tandem Trifluoromethylation/Semipinacol Rearrangement of Allylic Alcohols"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418520957466752","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Metal‐Free Aryltrifluoromethylation of Activated Alkenes"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418521004694656","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Trifluoromethylation Reactions for the Synthesis of β‐Trifluoromethylamines"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418521371593216","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A New H<sub>2</sub>O<sub>2</sub>/Acid Anhydride System for the Iodoarene-Catalyzed C−C Bond-Forming Reactions of Phenols"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699993566303488","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Iron-catalyzed trifluoromethylation with concomitant C–C bond formation via 1,2-migration of an aryl group"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699994770692608","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The chemistry of diacyl peroxides IX. An ESR study of the reduction of polyfluorodiacyl peroxides by copper (O) in the presence of 2-nitro-2-nitrosopropane: The generation of polyfluoroalkyl nitroalkyl nitroxides"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699995546639232","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Copper-Mediated Cyanotrifluoromethylation of Styrenes Using the Togni Reagent"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699995671969280","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Trifluoromethylation Reactions for the Synthesis of β‐Trifluoromethylamines"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981468591399936","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Metal-free radical perfluoroalkylation of (hetero)arenes"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981469532476672","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Copper-Catalyzed Intermolecular Trifluoromethylarylation of Alkenes: Mutual Activation of Arylboronic Acid and CF<sub>3</sub><sup>+</sup> Reagent"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981469658361472","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Electrophilic Trifluoromethylation by Use of Hypervalent Iodine Reagents"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981469802617472","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Recent advance in transition-metal-mediated trifluoromethylation for the construction of C(sp3)–CF3 bonds"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981470085348096","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"New Methods of Free-Radical Perfluoroalkylation of Aromatics and Alkenes. Absolute Rate Constants and Partial Rate Factors for the Homolytic Aromatic Substitution by <i>n</i>-Perfluorobutyl Radical"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981470208989824","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A NEW, FACILE METHOD FOR DETRIFLUOROACETYLATION OF ESTERS WITH TRIETHYLAMINE PRETREATED SILICA GEL"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981470574579968","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Metal-Free Direct Intramolecular Carbotrifluoromethylation of Alkenes to Functionalized Trifluoromethyl Azaheterocycles"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981470959543680","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Copper‐Catalyzed Trifluoromethylation of Unactivated Olefins"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981470969891072","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Copper-catalyzed trifluoromethylation of N-arylacrylamides “on water” at room temperature"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262944554979584","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis of Oxindoles through Silver‐Catalyzed Trifluoromethylation–, Difluoromethylation– and Arylsulfonylation–Cyclization Reaction of <i>N</i>‐Arylacrylamides"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544420484146688","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Oxidative Trifluoromethylation and Trifluoromethylthiolation Reactions Using (Trifluoromethyl)trimethylsilane as a Nucleophilic CF<sub>3</sub> Source"}]},{"@id":"https://cir.nii.ac.jp/crid/1362825894033811200","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Product Control in Alkene Trifluoromethylation: Hydrotrifluoromethylation, Vinylic Trifluoromethylation, and Iodotrifluoromethylation using Togni Reagent"}]},{"@id":"https://cir.nii.ac.jp/crid/1362825894389551744","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Trifluormethylierung von Alkenen unter gleichzeitiger Einführung weiterer funktioneller Gruppen"}]},{"@id":"https://cir.nii.ac.jp/crid/1362825894528121984","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Fluorine in Medicinal Chemistry and Chemical Biology"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107369667064704","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Direct C2-trifluoromethylation of indole derivatives catalyzed by copper acetate"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107370215659904","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Copper-Catalyzed C(sp<sup>3</sup>)–C(sp<sup>3</sup>) Bond Formation Using a Hypervalent Iodine Reagent: An Efficient Allylic Trifluoromethylation"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107370954486144","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Copper‐Catalyzed Trifluoromethylation‐Initiated Radical 1,2‐Aryl Migration in α,α‐Diaryl Allylic Alcohols"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107371246212352","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Visible‐Light‐Induced Trifluoromethylation of <i>N</i>‐Aryl Acrylamides: A Convenient and Effective Method To Synthesize CF<sub>3</sub>‐Containing Oxindoles Bearing a Quaternary Carbon Center"}]},{"@id":"https://cir.nii.ac.jp/crid/1363388843982782592","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A scalable and operationally simple radical trifluoromethylation"}]},{"@id":"https://cir.nii.ac.jp/crid/1363388844021658240","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Rapid Trifluoromethylation of Indole Derivatives"}]},{"@id":"https://cir.nii.ac.jp/crid/1363388844148954624","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Dual Catalysis with Copper and Rhenium for Trifluoromethylation of Propargylic Alcohols: Efficient Synthesis of α‐Trifluoromethylated Enones"}]},{"@id":"https://cir.nii.ac.jp/crid/1363388845901812864","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Metal‐Free Aryltrifluoromethylation of Activated Alkenes"}]},{"@id":"https://cir.nii.ac.jp/crid/1363670318957211264","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Copper‐Catalyzed Trifluoromethylation–Cyclization of Enynes: Highly Regioselective Construction of Trifluoromethylated Carbocycles and Heterocycles"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951793214860928","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Addition of CF<sub>3</sub> across unsaturated moieties: a powerful functionalization tool"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951794638873344","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Trifluoromethylation by bis(trifluoroacetyl) peroxide of polymers bearing benzene rings"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951795816230016","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Fluorine in health care: Organofluorine containing blockbuster drugs"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951796065468544","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Application of Langlois’ Reagent in Trifluoromethylation Reactions"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951796252233472","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Alkene Trifluoromethylation Coupled with CC Bond Formation: Construction of Trifluoromethylated Carbocycles and Heterocycles"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233268180358400","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Copper‐Catalyzed Trifluoromethylation and Cyclization of Aromatic‐Sulfonyl‐Group‐Tethered Alkenes for the Construction of 1,2‐Benzothiazinane Dioxide Type Compounds"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233268585106560","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Trifluoromethyltrimethylsilane: Nucleophilic Trifluoromethylation and Beyond"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233269373059584","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Copper‐Catalyzed Tandem Trifluoromethylation/Semipinacol Rearrangement of Allylic Alcohols"}]},{"@id":"https://cir.nii.ac.jp/crid/1390282679555815552","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@language":"en","@value":"HEPTAFLUOROPROPYLATION OF ELECTRON-RICH OLEFINS WITH BIS(HEPTAFLUOROBUTYRYL) PEROXIDE"}]},{"@id":"https://cir.nii.ac.jp/crid/1390285300161209344","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Fluorofunctionalizations of C–C Multiple Bonds  and C–H Bonds"}]},{"@id":"https://cir.nii.ac.jp/crid/2050307417118353152","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of trifluoromethylated B12 derivative and photolysis of cobalt(Ⅲ)-trifluoromethyl bond"}]},{"@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":"10.1002/anie.201604127"},{"@type":"KAKEN","@value":"PRODUCT-21293547"},{"@type":"CROSSREF","@value":"10.1246/bcsj.20190080_references_DOI_2sUmK1wogDpq2Lez2J62OiO7GQD"},{"@type":"CROSSREF","@value":"10.1055/a-2029-0345_references_DOI_2sUmK1wogDpq2Lez2J62OiO7GQD"},{"@type":"CROSSREF","@value":"10.1002/anie.202407150_references_DOI_2sUmK1wogDpq2Lez2J62OiO7GQD"},{"@type":"CROSSREF","@value":"10.1248/cpb.c19-00856_references_DOI_2sUmK1wogDpq2Lez2J62OiO7GQD"},{"@type":"CROSSREF","@value":"10.1002/adsc.202300337_references_DOI_2sUmK1wogDpq2Lez2J62OiO7GQD"},{"@type":"CROSSREF","@value":"10.1246/cl.180355_references_DOI_2sUmK1wogDpq2Lez2J62OiO7GQD"},{"@type":"CROSSREF","@value":"10.1039/d1ob01529j_references_DOI_2sUmK1wogDpq2Lez2J62OiO7GQD"},{"@type":"CROSSREF","@value":"10.1002/adsc.202201268_references_DOI_2sUmK1wogDpq2Lez2J62OiO7GQD"},{"@type":"CROSSREF","@value":"10.1002/tcr.202300202_references_DOI_2sUmK1wogDpq2Lez2J62OiO7GQD"},{"@type":"CROSSREF","@value":"10.1016/j.jfluchem.2017.07.012_references_DOI_2sUmK1wogDpq2Lez2J62OiO7GQD"},{"@type":"CROSSREF","@value":"10.1021/acs.joc.7b02307_references_DOI_2sUmK1wogDpq2Lez2J62OiO7GQD"}]}