{"@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/1360004233249877504.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1021/ol503616y"}},{"identifier":{"@type":"URI","@value":"https://pubs.acs.org/doi/pdf/10.1021/ol503616y"}},{"identifier":{"@type":"DOI","@value":"10.1002/chin.201529150"}},{"identifier":{"@type":"PMID","@value":"25685938"}}],"resourceType":"学術雑誌論文(journal article)","dc:title":[{"@value":"Copper-Catalyzed Regioselective Trifluoromethylthiolation of Pyrroles by Trifluoromethanesulfonyl Hypervalent Iodonium Ylide"}],"description":[{"notation":[{"@value":"The copper-catalyzed trifluoromethylthiolation of pyrroles with a trifluoromethanesulfonyl hypervalent iodonium ylide under mild conditions has been achieved. A broad set of pyrroles could be transformed to the corresponding products in moderate to excellent yields. The reaction mechanism is hypothesized."}]}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1380004233249877376","@type":"Researcher","foaf:name":[{"@value":"Zhongyan Huang"}],"jpcoar:affiliationName":[{"@value":"Department\rof Nanopharmaceutical\rSciences, Nagoya Institute of Technology, Gokiso, Showa-ku, Nagoya466-8555, Japan"}]},{"@id":"https://cir.nii.ac.jp/crid/1380004233249877377","@type":"Researcher","foaf:name":[{"@value":"Yu-Dong Yang"}],"jpcoar:affiliationName":[{"@value":"Department\rof Nanopharmaceutical\rSciences, Nagoya Institute of Technology, Gokiso, Showa-ku, Nagoya466-8555, Japan"}]},{"@id":"https://cir.nii.ac.jp/crid/1380004233249877504","@type":"Researcher","foaf:name":[{"@value":"Etsuko Tokunaga"}],"jpcoar:affiliationName":[{"@value":"Department\rof Nanopharmaceutical\rSciences, Nagoya Institute of Technology, Gokiso, Showa-ku, Nagoya466-8555, Japan"}]},{"@id":"https://cir.nii.ac.jp/crid/1420845751139382656","@type":"Researcher","personIdentifier":[{"@type":"KAKEN_RESEARCHERS","@value":"40293302"},{"@type":"NRID","@value":"1000040293302"},{"@type":"NRID","@value":"9000403595999"},{"@type":"NRID","@value":"9000318134974"},{"@type":"NRID","@value":"9000254706184"},{"@type":"NRID","@value":"9000402014470"},{"@type":"NRID","@value":"9000406560003"},{"@type":"NRID","@value":"9000411023085"},{"@type":"NRID","@value":"9000411564783"},{"@type":"NRID","@value":"9000016657218"},{"@type":"NRID","@value":"9000005218519"},{"@type":"NRID","@value":"9000005162824"},{"@type":"NRID","@value":"9000005183653"},{"@type":"NRID","@value":"9000403596895"},{"@type":"NRID","@value":"9000403596661"},{"@type":"NRID","@value":"9000345347481"},{"@type":"NRID","@value":"9000257722717"},{"@type":"NRID","@value":"9000016581923"},{"@type":"NRID","@value":"9000254700033"},{"@type":"NRID","@value":"9000242708700"},{"@type":"NRID","@value":"9000005162404"},{"@type":"NRID","@value":"9000403595741"},{"@type":"NRID","@value":"9000403597089"},{"@type":"NRID","@value":"9000402006354"},{"@type":"NRID","@value":"9000018232852"},{"@type":"NRID","@value":"9000005198550"},{"@type":"NRID","@value":"9000021043644"},{"@type":"NRID","@value":"9000254705287"},{"@type":"NRID","@value":"9000254715242"},{"@type":"NRID","@value":"9000412664921"},{"@type":"NRID","@value":"9000403596948"},{"@type":"NRID","@value":"9000399261596"},{"@type":"NRID","@value":"9000254703064"},{"@type":"NRID","@value":"9000401805486"},{"@type":"NRID","@value":"9000017113622"},{"@type":"NRID","@value":"9000345430074"},{"@type":"NRID","@value":"9000403595234"},{"@type":"NRID","@value":"9000254241888"},{"@type":"NRID","@value":"9000257730218"},{"@type":"NRID","@value":"9000254705662"},{"@type":"NRID","@value":"9000401678346"},{"@type":"NRID","@value":"9000403594819"},{"@type":"NRID","@value":"9000242086843"},{"@type":"NRID","@value":"9000408634713"},{"@type":"NRID","@value":"9000020321464"},{"@type":"NRID","@value":"9000403595905"},{"@type":"NRID","@value":"9000391612851"},{"@type":"NRID","@value":"9000403596890"},{"@type":"NRID","@value":"9000403597240"},{"@type":"NRID","@value":"9000254240435"},{"@type":"NRID","@value":"9000403595227"},{"@type":"NRID","@value":"9000257732179"},{"@type":"RESEARCHMAP","@value":"https://researchmap.jp/nozshiba"}],"foaf:name":[{"@value":"Norio Shibata"}],"jpcoar:affiliationName":[{"@value":"Department\rof Nanopharmaceutical\rSciences, Nagoya Institute of Technology, Gokiso, Showa-ku, Nagoya466-8555, Japan"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"15237060"},{"@type":"EISSN","@value":"15237052"},{"@type":"PISSN","@value":"09317597"},{"@type":"EISSN","@value":"15222667"}],"prism:publicationName":[{"@value":"Organic Letters"}],"dc:publisher":[{"@value":"American Chemical Society (ACS)"}],"prism:publicationDate":"2015-02-16","prism:volume":"17","prism:number":"5","prism:startingPage":"1094","prism:endingPage":"1097"},"reviewed":"false","url":[{"@id":"https://pubs.acs.org/doi/pdf/10.1021/ol503616y"}],"createdAt":"2015-02-16","modifiedAt":"2023-04-15","project":[{"@id":"https://cir.nii.ac.jp/crid/1040000782243370752","@type":"Project","projectIdentifier":[{"@type":"KAKEN","@value":"25288045"},{"@type":"JGN","@value":"JP25288045"},{"@type":"URI","@value":"https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-25288045/"}],"notation":[{"@language":"ja","@value":"ハロゲン引力を駆動力とする触媒の開発と不斉炭素の構築"},{"@language":"en","@value":"Development of novel catalysts inducing halogen bonding and its application for asymmetric synthesis."}]},{"@id":"https://cir.nii.ac.jp/crid/1040000782267638016","@type":"Project","projectIdentifier":[{"@type":"KAKEN","@value":"25670055"},{"@type":"JGN","@value":"JP25670055"},{"@type":"URI","@value":"https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-25670055/"}],"notation":[{"@language":"ja","@value":"フッ素官能基の導入による小分子生理活性物質のナノコロイド化"},{"@language":"en","@value":"Study for the colloidal nanoparticles of drug molecules by fluoro-functionalization"}]}],"relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1050025031476838272","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Cp*Co-III-catalyzed directed C-H trifluoromethylthiolation of 2-phenylpyridines and 6-arylpurines"},{"@value":"Cp*Co<sup>III</sup>-catalyzed directed C–H trifluoromethylthiolation of 2-phenylpyridines and 6-arylpurines"}]},{"@id":"https://cir.nii.ac.jp/crid/1360011142935160960","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Introduction of Fluorine and Fluorine‐Containing Functional Groups"}]},{"@id":"https://cir.nii.ac.jp/crid/1360011144769814400","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"<i>N</i>‐Trifluoromethylthiophthalimide: A Stable Electrophilic SCF<sub>3</sub>‐Reagent and its Application in the Catalytic Asymmetric Trifluoromethylsulfenylation"}]},{"@id":"https://cir.nii.ac.jp/crid/1360011145383704576","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Understanding organofluorine chemistry. An introduction to the C–F bond"}]},{"@id":"https://cir.nii.ac.jp/crid/1360011146202531584","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Electrophilic trifluoromethanesulfanylation of indole derivatives"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285704871055872","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of Billard–Langlois Reagents and their Derivatives by Copper‐Catalyzed <i>N</i>‐Trifluoromethylthiolation of Arylamines with a Trifluoromethanesulfonyl Hypervalent Iodonium Ylide"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285708107775104","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of Sulfur Perfluorophenyl Compounds Using a Pentafluorobenzenesulfonyl Hypervalent Iodonium Ylide"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292618615113984","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis of stable arsonium and sulfur ylides from perfluoroalkanesulfonyl diazocarbonyl compounds and their X-ray diffraction analysis"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292619148195200","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Palladium-Catalyzed Trifluoromethylthiolation of Aryl C–H Bonds"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292619285188352","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Electrophilic <i>S</i>‐Trifluoromethylation of Cysteine Side Chains in <i>α</i>‐ and <i>β</i>‐Peptides: Isolation of Trifluoro‐methylated <i>Sandostatin</i><sup>®</sup> (Octreotide) Derivatives"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292619317276160","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Assessment of heat-sensitive thiophosphate protecting groups in the development of thermolytic DNA oligonucleotide prodrugs"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292620215030912","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Silver‐Catalyzed Decarboxylative Trifluoromethylthiolation of Aliphatic Carboxylic Acids in Aqueous Emulsion"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292620573870592","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Enantioselective Electrophilic Trifluoromethylthiolation of β‐Ketoesters: A Case of Reactivity and Selectivity Bias for Organocatalysis"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292620810481536","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Guide to Fluorine NMR for Organic Chemists"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292620909732992","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Copper‐Catalyzed Trifluoromethyl Thiolation—Mild and Efficient Synthesis of Trifluoromethyl Thioethers"}]},{"@id":"https://cir.nii.ac.jp/crid/1360565166589000960","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthetic Methods for Compounds Having CF<sub>3</sub>–S Units on Carbon by Trifluoromethylation, Trifluoromethylthiolation, Triflylation, and Related Reactions"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567183084051072","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Mechanistic Studies on the Generation and Properties of Superelectrophilic Singlet Carbenes from Bis(perfluoroalkanesulfonyl)bromonium Ylides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574093909476224","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Modern Fluoroorganic Chemistry"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574094649574144","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Pyrroles and their Benzo Derivatives: Applications"}]},{"@id":"https://cir.nii.ac.jp/crid/1360846640942721024","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Robust synthesis of trifluoromethionine and its derivatives by reductive trifluoromethylation of amino acid disulfides by CF3I/Na/Liq.NH3 system"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855569193378176","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Pd‐Catalyzed Synthesis of ArSCF<sub>3</sub> Compounds under Mild Conditions"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855570623148544","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis and Properties of Bis-(trifluoromethylthio)-mercury"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137043958399744","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Mild Electrophilic Trifluoromethylation of Carbon‐ and Sulfur‐Centered Nucleophiles by a Hypervalent Iodine(III)–CF<sub>3</sub> Reagent"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137044158022144","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthese und oxidation von 7-trifluormethylthiocycloheptatrien"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137044241246208","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Organofluorine Chemistry"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137044345146112","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Trifluoromethanesulfanylamides as Easy‐to‐Handle Equivalents of the Trifluoromethanesulfanyl Cation (CF<sub>3</sub>S<sup>+</sup>): Reaction with Alkenes and Alkynes"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137044403795968","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Aryl Fluoroalkyl Sulfides. II. Preparation by Condensation of Trifluoromethanesulfenyl Chloride with Aromatic Systems"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137045852028032","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Formation of CSCF<sub>3</sub> Bonds through Direct Trifluoromethylthiolation"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137046248576768","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Copper-catalyzed trifluoromethylthiolation of aryl and vinyl boronic acids with a shelf-stable electrophilic trifluoromethylthiolating reagent"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137046548352768","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Structural Reevaluation of the Electrophilic Hypervalent Iodine Reagent for Trifluoromethylthiolation Supported by the Crystalline Sponge Method for X‐ray Analysis"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418518614003456","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Metal-Free Oxidative Trifluoromethylthiolation of Terminal Alkynes with CF<sub>3</sub>SiMe<sub>3</sub> and Elemental Sulfur"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418518765516288","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Trifluoromethanesulfonyl Hypervalent Iodonium Ylide for Copper-Catalyzed Trifluoromethylthiolation of Enamines, Indoles, and β-Keto Esters"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418519580384128","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Copper–Boxmi Complexes as Highly Enantioselective Catalysts for Electrophilic Trifluoromethylthiolations"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418521116909952","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis of Phenothiazines. III. Derivatives of Hydroxy- and Mercaptophenothiazines<sup>1</sup>"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699993666281984","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Modular Synthesis of Lamellarins via Regioselective Assembly of 3,4,5-Differentially Arylated Pyrrole-2-carboxylates"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699994789831168","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Nickel-Catalyzed Synthesis of Aryl Trifluoromethyl Sulfides at Room Temperature"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699995125042176","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"SRN1 substitutions of halogenoperfluoroalkanes (CF3Br or CF2 Cl2) under pressure"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699995262348928","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Direct Catalytic Trifluoromethylthiolation of Boronic Acids and Alkynes Employing Electrophilic Shelf‐Stable <i>N</i>‐(trifluoromethylthio)phthalimide"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699995313073152","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"An Air‐Stable Copper Reagent for Nucleophilic Trifluoromethylthiolation of Aryl Halides"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699996226702208","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Organofluorine Compounds"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699996407990784","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Microwave-assisted aliphatic fluorine–chlorine exchange using triethylamine trihydrofluoride (TREAT-HF)"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981468809515648","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Recent advances in transition metal-catalyzed Csp<sup>2</sup>-monofluoro-, difluoro-, perfluoromethylation and trifluoromethylthiolation"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981469690909952","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The reaction of β-dicarbonyl compounds with trifluoromethylsulphenyl chloride. Part I. CF3S-substituted esters, anilides of β-keto acids, and their Schiff bases: Synthesis and stability."}]},{"@id":"https://cir.nii.ac.jp/crid/1361981469839518336","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Base‐Catalyzed Electrophilic Trifluoromethylthiolation of Terminal Alkynes"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981469880710144","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"<i>N</i>‐Trifluoromethylthiosaccharin: An Easily Accessible, Shelf‐Stable, Broadly Applicable Trifluoromethylthiolating Reagent"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981470860553984","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Recent advances in the trifluoromethylation methodology and new CF3-containing drugs"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262943676040960","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Recent advances in the synthesis of pyrroles by multicomponent reactions"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262944670713344","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"An Electrophilic Hypervalent Iodine Reagent for Trifluoromethylthiolation"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544418878283008","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Trifluoromethylthiodediazoniation: a simple, efficient route to trifluoromethyl aryl sulfides"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544419121771648","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Aromatic and heterocyclic perfluoroalkyl sulfides. Methods of preparation"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544419584803840","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Direct Trifluoromethylthiolation Reactions: The “Renaissance” of an Old Concept"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544420135217408","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Preparation of Trifluoromethyl Aryl Sulfides Using Silver(I) Trifluoromethanethiolate and an Inorganic Iodide"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544420612458752","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Perhalogenmethylthio‐Heterocyclen, VIII. (Perchlorfluormethylthio)‐ und (Halogenformylthio)‐N‐Heteroaromaten"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544420702941056","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Electrophilic Trifluoromethanesulfanylation of Organometallic Species with Trifluoromethanesulfanamides"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544421152195968","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Highly Regioselective Migration of the Sulfonyl Group: Easy Access to Functionalized Pyrroles"}]},{"@id":"https://cir.nii.ac.jp/crid/1362825895844567168","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Organofluorine Chemistry"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107368687441280","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis of 2-, 3- and 9-substituted 11-oxo-11H-pyrrolo[2,1-b][3]benzazepines"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107368942076672","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A New and Convenient Synthesis of<i>S</i>-Trifluoromethyl-Containing Amino Acids"}]},{"@id":"https://cir.nii.ac.jp/crid/1363388843703481216","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Fluorine in Pharmaceutical Industry: Fluorine-Containing Drugs Introduced to the Market in the Last Decade (2001–2011)"}]},{"@id":"https://cir.nii.ac.jp/crid/1363388845631003776","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The reaction of cyclic β-diketones with trifluoromethylsulphenyl chloride"}]},{"@id":"https://cir.nii.ac.jp/crid/1363670319620490112","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Perhalogenmethylthioheterocyclen. XI: CF3S-substituierte N-methyl-pyrrole; migration der CF3S-gruppe"}]},{"@id":"https://cir.nii.ac.jp/crid/1363670320474774272","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Über organische Fluorverbindungen"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951793690137856","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Oxidative Trifluoromethylthiolation of Terminal Alkynes with AgSCF<sub>3</sub>: A Convenient Approach to Alkynyl Trifluoromethyl Sulfides"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951795049068160","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A sustainable catalytic pyrrole synthesis"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951795163035136","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Electrophilic Trifluoromethylthiolation of Carbonyl Compounds"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233268796356864","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"(Perhalogenmethylthio)heterocyclen. X. Säurekatalysierte Substitutionen an (Perchlorfluormethylthio)pyrrolen und deren agrobiologische Wirkung"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233271068820992","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis of natural products containing the pyrrolic ring"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233271183417472","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Direct electrophilic <i>N</i>-trifluoromethylthiolation of amines with trifluoromethanesulfenamide"}]},{"@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"}]}],"dataSourceIdentifier":[{"@type":"CROSSREF","@value":"10.1021/ol503616y"},{"@type":"KAKEN","@value":"PRODUCT-14983049"},{"@type":"KAKEN","@value":"PRODUCT-15123024"},{"@type":"OPENAIRE","@value":"doi_dedup___::dd001f92aeebb889da13d7ef48c81e57"},{"@type":"CROSSREF","@value":"10.1039/c7cc03072j_references_DOI_TweplLMYusK1wFKyKnKEGe8ejOo"},{"@type":"CROSSREF","@value":"10.1002/ajoc.201500067_references_DOI_TweplLMYusK1wFKyKnKEGe8ejOo"},{"@type":"CROSSREF","@value":"10.1246/bcsj.20160223_references_DOI_TweplLMYusK1wFKyKnKEGe8ejOo"},{"@type":"CROSSREF","@value":"10.1021/acs.joc.6b00142_references_DOI_TweplLMYusK1wFKyKnKEGe8ejOo"},{"@type":"CROSSREF","@value":"10.1021/acs.joc.7b01908_references_DOI_TweplLMYusK1wFKyKnKEGe8ejOo"}]}