{"title":"以铜作为位点选择性序贯光氧还原剂-光诱导剂,实现具有马尔科夫尼科夫选择性的瓦克型苯乙烯氧化反应","authors":"","doi":"10.1039/d4cy00590b","DOIUrl":null,"url":null,"abstract":"<div><p>We report a palladium-free Wacker-type oxidation of styrenes using CuCl<sub>2</sub>/KBr as the catalyst and trichloroisocyanuric acid as a stoichiometric chlorine radical source. The reaction protocol is compatible with diverse functional groups, affording selectively acetophenones. The mechanistic analysis revealed that a site-selective sequential Cu<sup>II</sup>-photooxidation/Cu<sup>I</sup>-photoreduction of the intermediary chlorohydrin is the key to the success of this transformation.</p></div>","PeriodicalId":66,"journal":{"name":"Catalysis Science & Technology","volume":null,"pages":null},"PeriodicalIF":4.4000,"publicationDate":"2024-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Wacker-type oxidation of styrenes with Markovnikov selectivity using copper as a site-selective sequential photooxidant–photoreductant†\",\"authors\":\"\",\"doi\":\"10.1039/d4cy00590b\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>We report a palladium-free Wacker-type oxidation of styrenes using CuCl<sub>2</sub>/KBr as the catalyst and trichloroisocyanuric acid as a stoichiometric chlorine radical source. The reaction protocol is compatible with diverse functional groups, affording selectively acetophenones. The mechanistic analysis revealed that a site-selective sequential Cu<sup>II</sup>-photooxidation/Cu<sup>I</sup>-photoreduction of the intermediary chlorohydrin is the key to the success of this transformation.</p></div>\",\"PeriodicalId\":66,\"journal\":{\"name\":\"Catalysis Science & Technology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.4000,\"publicationDate\":\"2024-07-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Catalysis Science & Technology\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S2044475324003447\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Science & Technology","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2044475324003447","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Wacker-type oxidation of styrenes with Markovnikov selectivity using copper as a site-selective sequential photooxidant–photoreductant†
We report a palladium-free Wacker-type oxidation of styrenes using CuCl2/KBr as the catalyst and trichloroisocyanuric acid as a stoichiometric chlorine radical source. The reaction protocol is compatible with diverse functional groups, affording selectively acetophenones. The mechanistic analysis revealed that a site-selective sequential CuII-photooxidation/CuI-photoreduction of the intermediary chlorohydrin is the key to the success of this transformation.
期刊介绍:
A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis.
Editor-in-chief: Bert Weckhuysen
Impact factor: 5.0
Time to first decision (peer reviewed only): 31 days