{"title":"铬(II)催化缩醛与α-三氟甲基烯烃的脱氟还原交偶联。","authors":"Zaiyang Li, Meiming Luo and Xiaoming Zeng","doi":"10.1039/D5OB00547G","DOIUrl":null,"url":null,"abstract":"<p >We report here the chromium(<small>II</small>)-catalyzed defluorinative reductive cross-coupling reaction of acetals with α-trifluoromethyl alkenes. α-Alkoxyalkyl radicals are generated from acetals under the synergistic effect of catalytic chromium and trimethylsilyl chloride. Subsequent selective cross-coupling of the radicals with α-trifluoromethyl alkenes provides a synthetic route to <em>gem</em>-difluoroalkenes that contain an alkoxy substituent at the homoallylic position.</p>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":" 22","pages":" 5293-5297"},"PeriodicalIF":2.9000,"publicationDate":"2025-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Chromium(ii)-catalyzed defluorinative reductive cross-coupling of acetals with α-trifluoromethyl alkenes†\",\"authors\":\"Zaiyang Li, Meiming Luo and Xiaoming Zeng\",\"doi\":\"10.1039/D5OB00547G\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >We report here the chromium(<small>II</small>)-catalyzed defluorinative reductive cross-coupling reaction of acetals with α-trifluoromethyl alkenes. α-Alkoxyalkyl radicals are generated from acetals under the synergistic effect of catalytic chromium and trimethylsilyl chloride. Subsequent selective cross-coupling of the radicals with α-trifluoromethyl alkenes provides a synthetic route to <em>gem</em>-difluoroalkenes that contain an alkoxy substituent at the homoallylic position.</p>\",\"PeriodicalId\":96,\"journal\":{\"name\":\"Organic & Biomolecular Chemistry\",\"volume\":\" 22\",\"pages\":\" 5293-5297\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2025-05-07\",\"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/d5ob00547g\",\"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/d5ob00547g","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Chromium(ii)-catalyzed defluorinative reductive cross-coupling of acetals with α-trifluoromethyl alkenes†
We report here the chromium(II)-catalyzed defluorinative reductive cross-coupling reaction of acetals with α-trifluoromethyl alkenes. α-Alkoxyalkyl radicals are generated from acetals under the synergistic effect of catalytic chromium and trimethylsilyl chloride. Subsequent selective cross-coupling of the radicals with α-trifluoromethyl alkenes provides a synthetic route to gem-difluoroalkenes that contain an alkoxy substituent at the homoallylic position.
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.