{"@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/1390569612379999744.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1584/jpestics.d21-012"}},{"identifier":{"@type":"NDL_BIB_ID","@value":"031472884"}},{"identifier":{"@type":"URI","@value":"http://id.ndl.go.jp/bib/031472884"}},{"identifier":{"@type":"URI","@value":"https://ndlsearch.ndl.go.jp/books/R000000004-I031472884"}},{"identifier":{"@type":"URI","@value":"https://www.jstage.jst.go.jp/article/jpestics/46/2/46_D21-012/_pdf"}},{"identifier":{"@type":"PMID","@value":"34135675"}},{"identifier":{"@type":"NAID","@value":"130008043165"}},{"identifier":{"@type":"URI","@value":"https://search.jamas.or.jp/link/ui/2022035738"}}],"dc:title":[{"@language":"en","@value":"Synthesis and application of trifluoromethylpyridines as a key structural motif in active agrochemical and pharmaceutical ingredients"}],"dc:language":"en","description":[{"type":"abstract","notation":[{"@language":"en","@value":"<p>Herein, we provide a brief overview of the synthesis and applications of trifluoromethylpyridine (TFMP) and its derivatives in the agrochemical and pharmaceutical industries. Currently, the major use of TFMP derivatives is in the protection of crops from pests. Fluazifop-butyl was the first TFMP derivative introduced to the agrochemical market, and since then, more than 20 new TFMP-containing agrochemicals have acquired ISO common names. Several TFMP derivatives are also used in the pharmaceutical and veterinary industries; five pharmaceutical and two veterinary products containing the TFMP moiety have been granted market approval, and many candidates are currently undergoing clinical trials. The biological activities of TFMP derivatives are thought to be due to the combination of the unique physicochemical properties of the fluorine atom and the unique characteristics of the pyridine moiety. It is expected that many novel applications of TFMP will be discovered in the future.</p>"}],"abstractLicenseFlag":"disallow"}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1410569612379999746","@type":"Researcher","personIdentifier":[{"@type":"NRID","@value":"9000412276424"}],"foaf:name":[{"@language":"en","@value":"Tsukamoto Masamitsu"}],"jpcoar:affiliationName":[{"@language":"en","@value":"Bioscience Business Headquarters, Ishihara Sangyo Kaisha, Ltd."}]},{"@id":"https://cir.nii.ac.jp/crid/1410569612379999745","@type":"Researcher","personIdentifier":[{"@type":"NRID","@value":"9000412276425"}],"foaf:name":[{"@language":"en","@value":"Nakamura Tadashi"}],"jpcoar:affiliationName":[{"@language":"en","@value":"Bioscience Business Headquarters, Ishihara Sangyo Kaisha, Ltd."}]},{"@id":"https://cir.nii.ac.jp/crid/1410569612379999747","@type":"Researcher","personIdentifier":[{"@type":"NRID","@value":"9000412276426"}],"foaf:name":[{"@language":"en","@value":"Kimura Hirohiko"}],"jpcoar:affiliationName":[{"@language":"en","@value":"Central Research Institute, Ishihara Sangyo Kaisha, Ltd."}]},{"@id":"https://cir.nii.ac.jp/crid/1410569612379999744","@type":"Researcher","personIdentifier":[{"@type":"NRID","@value":"9000412276427"}],"foaf:name":[{"@language":"en","@value":"Nakayama Hitoshi"}],"jpcoar:affiliationName":[{"@language":"en","@value":"Healthcare Business Development Headquarters, Ishihara Sangyo Kaisha, Ltd."}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"1348589X"},{"@type":"EISSN","@value":"13490923"},{"@type":"CODEN","@value":"JPSTCF"},{"@type":"NDL_BIB_ID","@value":"024474293"},{"@type":"ISSN","@value":"1348589X"},{"@type":"LISSN","@value":"03851559"},{"@type":"NCID","@value":"AA11818622"}],"prism:publicationName":[{"@language":"en","@value":"Journal of Pesticide Science"},{"@language":"ja","@value":"日本農薬学会誌（Ｊｏｕｒｎａｌ　ｏｆ　Ｐｅｓｔｉｃｉｄｅ　Ｓｃｉｅｎｃｅ）"},{"@language":"en","@value":"J. Pestic. Sci."},{"@language":"en","@value":"Journal of Pesticide Science"},{"@language":"ja","@value":"日本農薬学会誌（Ｊｏｕｒｎａｌ　ｏｆ　Ｐｅｓｔｉｃｉｄｅ　Ｓｃｉｅｎｃｅ）"}],"dc:publisher":[{"@language":"en","@value":"Pesticide Science Society of Japan"},{"@language":"ja","@value":"日本農薬学会"}],"prism:publicationDate":"2021-05-20","prism:volume":"46","prism:number":"2","prism:startingPage":"125","prism:endingPage":"142"},"reviewed":"false","dcterms:accessRights":"http://purl.org/coar/access_right/c_abf2","url":[{"@id":"http://id.ndl.go.jp/bib/031472884"},{"@id":"https://ndlsearch.ndl.go.jp/books/R000000004-I031472884"},{"@id":"https://www.jstage.jst.go.jp/article/jpestics/46/2/46_D21-012/_pdf"},{"@id":"https://search.jamas.or.jp/link/ui/2022035738"}],"availableAt":"2021-05-20","foaf:topic":[{"@id":"https://cir.nii.ac.jp/all?q=trifluoromethylpyridine","dc:title":"trifluoromethylpyridine"},{"@id":"https://cir.nii.ac.jp/all?q=intermediate","dc:title":"intermediate"},{"@id":"https://cir.nii.ac.jp/all?q=chemical%20properties","dc:title":"chemical properties"},{"@id":"https://cir.nii.ac.jp/all?q=agrochemicals","dc:title":"agrochemicals"},{"@id":"https://cir.nii.ac.jp/all?q=pharmaceuticals","dc:title":"pharmaceuticals"},{"@id":"https://cir.nii.ac.jp/all?q=vapor%E2%80%93phase%20reaction","dc:title":"vapor–phase reaction"},{"@id":"https://cir.nii.ac.jp/all?q=trifluoromethylpyridine","dc:title":"trifluoromethylpyridine"},{"@id":"https://cir.nii.ac.jp/all?q=intermediate","dc:title":"intermediate"},{"@id":"https://cir.nii.ac.jp/all?q=chemical%20properties","dc:title":"chemical properties"},{"@id":"https://cir.nii.ac.jp/all?q=agrochemicals","dc:title":"agrochemicals"},{"@id":"https://cir.nii.ac.jp/all?q=pharmaceuticals","dc:title":"pharmaceuticals"},{"@id":"https://cir.nii.ac.jp/all?q=vapor%E2%80%93phase%20reaction","dc:title":"vapor–phase reaction"}],"relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1360011144033458688","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Recommendable Routes to 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Bioavailable, Pan-Class I PI3K/mTOR Inhibitor as Clinical Candidate in Oncology"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574096066399616","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis of a new class of pyridine herbicide"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574096465107968","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Herbicidal Activity of Fluazifop-Butyl, Haloxyfop-Methyl, and Sethoxydim in Soil"}]},{"@id":"https://cir.nii.ac.jp/crid/1360579813422763520","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of Pyridine-SF4-Alkynes via Light-Promoted Radical Coupling of Pyridine-SF4-Chlorides and EBX Reagents"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855568780550016","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Doravirine: a new non-nucleoside reverse transcriptase 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(<i>R</i>)-(1-(4-Fluorophenyl)-6-((1-methyl-1<i>H</i>-pyrazol-4-yl)sulfonyl)-4,4a,5,6,7,8-hexahydro-1<i>H</i>-pyrazolo[3,4-<i>g</i>]isoquinolin-4a-yl)(4-(trifluoromethyl)pyridin-2-yl)methanone (CORT125134): A Selective Glucocorticoid Receptor (GR) Antagonist"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418520266135424","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Process Development for the Sulfonamide Herbicide Pyroxsulam"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699993995996032","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"CBS9106 is a novel reversible oral CRM1 inhibitor with CRM1 degrading activity"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699994570235520","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Sulfoxaflor and the sulfoximine insecticides: Chemistry, mode of action and basis for efficacy on resistant 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