{"title":"三氟二乙烷与芳基-1,3-茚二酮反应中由试剂和溶剂控制的产物差异","authors":"Mumtaz Ahmad , Lubina Fatma , Ruchir Kant , Kishor Mohanan","doi":"10.1016/j.jfluchem.2024.110256","DOIUrl":null,"url":null,"abstract":"<div><p>An interesting product divergence in the reaction of trifluorodiazoethane with arylidene-1,3-indanediones is reported. The reaction conducted using 10 mol% of silver carbonate afforded trifluoromethylspiropyrazolines, while with excess of cesium fluoride in methanol, the cycloaddition was followed by nucleophilic ring opening of the spiropyrazoline to afford trifluoromethylated <em>o</em>-carbomethoxybenzoylpyrazolines. Both protocols work under mild reaction conditions and exhibit good functional group tolerance.</p></div>","PeriodicalId":357,"journal":{"name":"Journal of Fluorine Chemistry","volume":"274 ","pages":"Article 110256"},"PeriodicalIF":1.7000,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Reagent- and solvent-controlled product divergence in the reaction of trifluorodiazoethane with arylidene-1,3-indanediones\",\"authors\":\"Mumtaz Ahmad , Lubina Fatma , Ruchir Kant , Kishor Mohanan\",\"doi\":\"10.1016/j.jfluchem.2024.110256\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>An interesting product divergence in the reaction of trifluorodiazoethane with arylidene-1,3-indanediones is reported. The reaction conducted using 10 mol% of silver carbonate afforded trifluoromethylspiropyrazolines, while with excess of cesium fluoride in methanol, the cycloaddition was followed by nucleophilic ring opening of the spiropyrazoline to afford trifluoromethylated <em>o</em>-carbomethoxybenzoylpyrazolines. Both protocols work under mild reaction conditions and exhibit good functional group tolerance.</p></div>\",\"PeriodicalId\":357,\"journal\":{\"name\":\"Journal of Fluorine Chemistry\",\"volume\":\"274 \",\"pages\":\"Article 110256\"},\"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/S0022113924000174\",\"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/S0022113924000174","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
Reagent- and solvent-controlled product divergence in the reaction of trifluorodiazoethane with arylidene-1,3-indanediones
An interesting product divergence in the reaction of trifluorodiazoethane with arylidene-1,3-indanediones is reported. The reaction conducted using 10 mol% of silver carbonate afforded trifluoromethylspiropyrazolines, while with excess of cesium fluoride in methanol, the cycloaddition was followed by nucleophilic ring opening of the spiropyrazoline to afford trifluoromethylated o-carbomethoxybenzoylpyrazolines. Both protocols work under mild reaction conditions and exhibit good functional group tolerance.
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.