{"title":"钴催化全氟烷基乙烯的抗马尔可夫尼科夫选择性氢硼化反应","authors":"Renning Dong, Yangjie Huang, Liqin Wei, Lili Xie, Zhiqiang Weng","doi":"10.1021/acs.joc.5c00013","DOIUrl":null,"url":null,"abstract":"A facile protocol for <i>anti</i>-Markovnikov-selective hydroborylation of perfluoroalkylethylenes with pinacolborane has been developed in the presence of Co(acac)<sub>2</sub> and dppf in DMAC to furnish diverse perfluoroalkylethylboronate esters. Subsequently, perfluoroalkylethylboronate ester derivatives were further transformed into 2-perfluoroalkyl ethanol, amide, and cross-coupling products.","PeriodicalId":57,"journal":{"name":"Journal of Organic Chemistry","volume":"1 1","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2025-05-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cobalt-Catalyzed anti-Markovnikov-Selective Hydroborylation of Perfluoroalkylethylenes\",\"authors\":\"Renning Dong, Yangjie Huang, Liqin Wei, Lili Xie, Zhiqiang Weng\",\"doi\":\"10.1021/acs.joc.5c00013\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A facile protocol for <i>anti</i>-Markovnikov-selective hydroborylation of perfluoroalkylethylenes with pinacolborane has been developed in the presence of Co(acac)<sub>2</sub> and dppf in DMAC to furnish diverse perfluoroalkylethylboronate esters. Subsequently, perfluoroalkylethylboronate ester derivatives were further transformed into 2-perfluoroalkyl ethanol, amide, and cross-coupling products.\",\"PeriodicalId\":57,\"journal\":{\"name\":\"Journal of Organic Chemistry\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2025-05-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Organic Chemistry\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.joc.5c00013\",\"RegionNum\":2,\"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":"Journal of Organic Chemistry","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1021/acs.joc.5c00013","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Cobalt-Catalyzed anti-Markovnikov-Selective Hydroborylation of Perfluoroalkylethylenes
A facile protocol for anti-Markovnikov-selective hydroborylation of perfluoroalkylethylenes with pinacolborane has been developed in the presence of Co(acac)2 and dppf in DMAC to furnish diverse perfluoroalkylethylboronate esters. Subsequently, perfluoroalkylethylboronate ester derivatives were further transformed into 2-perfluoroalkyl ethanol, amide, and cross-coupling products.
期刊介绍:
Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.