{"title":"宝石-溴氟烯烃的光催化E→Z异构化:β-氟苯乙烯衍生物的立体选择性合成。","authors":"Hayato Kato, Yoshihito Kayaki and Takashi Koike","doi":"10.1039/D4OB01658K","DOIUrl":null,"url":null,"abstract":"<p >Stereoselective synthesis of β-fluorostyrene derivatives has been achieved. Selective isomerization of <em>gem</em>-bromofluoroalkenyl benzenes bearing various <em>ortho</em>-substituents is enabled by using Ir photocatalysts with high triplet energy. Subsequent one-pot transition-metal (TM)-catalyzed reactions enable pot-economical synthesis of monofluoroalkenes in a stereoselective manner.</p>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":" 6","pages":" 1342-1346"},"PeriodicalIF":2.7000,"publicationDate":"2024-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Photocatalytic E → Z isomerization of gem-bromofluoroalkenes: stereoselective synthesis of β-fluorostyrene derivatives†\",\"authors\":\"Hayato Kato, Yoshihito Kayaki and Takashi Koike\",\"doi\":\"10.1039/D4OB01658K\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Stereoselective synthesis of β-fluorostyrene derivatives has been achieved. Selective isomerization of <em>gem</em>-bromofluoroalkenyl benzenes bearing various <em>ortho</em>-substituents is enabled by using Ir photocatalysts with high triplet energy. Subsequent one-pot transition-metal (TM)-catalyzed reactions enable pot-economical synthesis of monofluoroalkenes in a stereoselective manner.</p>\",\"PeriodicalId\":96,\"journal\":{\"name\":\"Organic & Biomolecular Chemistry\",\"volume\":\" 6\",\"pages\":\" 1342-1346\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2024-12-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic & Biomolecular Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/ob/d4ob01658k\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic & Biomolecular Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/ob/d4ob01658k","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Photocatalytic E → Z isomerization of gem-bromofluoroalkenes: stereoselective synthesis of β-fluorostyrene derivatives†
Stereoselective synthesis of β-fluorostyrene derivatives has been achieved. Selective isomerization of gem-bromofluoroalkenyl benzenes bearing various ortho-substituents is enabled by using Ir photocatalysts with high triplet energy. Subsequent one-pot transition-metal (TM)-catalyzed reactions enable pot-economical synthesis of monofluoroalkenes in a stereoselective manner.
期刊介绍:
Organic & Biomolecular Chemistry is an international journal using integrated research in chemistry-organic chemistry. Founded in 2003 by the Royal Society of Chemistry, the journal is published in Semimonthly issues and has been indexed by SCIE, a leading international database. The journal focuses on the key research and cutting-edge progress in the field of chemistry-organic chemistry, publishes and reports the research results in this field in a timely manner, and is committed to becoming a window and platform for rapid academic exchanges among peers in this field. The journal's impact factor in 2023 is 2.9, and its CiteScore is 5.5.