{"title":"铱络合物对 N-乙酰氨基苯甲酸的串联脱羧/氟化反应","authors":"Tomohiko Shirai, Tomokazu Yamasaki","doi":"10.1016/j.jfluchem.2024.110260","DOIUrl":null,"url":null,"abstract":"<div><p>Decarboxylative transformations are valuable tools for carbon-heteroatom bond formation. However, synthetic applications of the decarboxylation of aromatic carboxylic acids to produce C(sp<sup>2</sup>)–F bonds remain limited. Herein, we propose a tandem catalytic decarboxylation/fluorination of N-acetylanthranilic acids to produce useful organofluorine compounds by using Ir(I)/bisphosphine complexes.</p></div>","PeriodicalId":357,"journal":{"name":"Journal of Fluorine Chemistry","volume":"274 ","pages":"Article 110260"},"PeriodicalIF":1.7000,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Tandem decarboxylation/fluorination of N-acetylanthranilic acids by iridium complexes\",\"authors\":\"Tomohiko Shirai, Tomokazu Yamasaki\",\"doi\":\"10.1016/j.jfluchem.2024.110260\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Decarboxylative transformations are valuable tools for carbon-heteroatom bond formation. However, synthetic applications of the decarboxylation of aromatic carboxylic acids to produce C(sp<sup>2</sup>)–F bonds remain limited. Herein, we propose a tandem catalytic decarboxylation/fluorination of N-acetylanthranilic acids to produce useful organofluorine compounds by using Ir(I)/bisphosphine complexes.</p></div>\",\"PeriodicalId\":357,\"journal\":{\"name\":\"Journal of Fluorine Chemistry\",\"volume\":\"274 \",\"pages\":\"Article 110260\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2024-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Fluorine Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0022113924000216\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Fluorine Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022113924000216","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
Tandem decarboxylation/fluorination of N-acetylanthranilic acids by iridium complexes
Decarboxylative transformations are valuable tools for carbon-heteroatom bond formation. However, synthetic applications of the decarboxylation of aromatic carboxylic acids to produce C(sp2)–F bonds remain limited. Herein, we propose a tandem catalytic decarboxylation/fluorination of N-acetylanthranilic acids to produce useful organofluorine compounds by using Ir(I)/bisphosphine complexes.
期刊介绍:
The Journal of Fluorine Chemistry contains reviews, original papers and short communications. The journal covers all aspects of pure and applied research on the chemistry as well as on the applications of fluorine, and of compounds or materials where fluorine exercises significant effects. This can include all chemistry research areas (inorganic, organic, organometallic, macromolecular and physical chemistry) but also includes papers on biological/biochemical related aspects of Fluorine chemistry as well as medicinal, agrochemical and pharmacological research. The Journal of Fluorine Chemistry also publishes environmental and industrial papers dealing with aspects of Fluorine chemistry on energy and material sciences. Preparative and physico-chemical investigations as well as theoretical, structural and mechanistic aspects are covered. The Journal, however, does not accept work of purely routine nature.
For reviews and special issues on particular topics of fluorine chemistry or from selected symposia, please contact the Regional Editors for further details.