Huangbin Sun , Chang Huang , Xueting Bin , Fuzhi Cui , Guofang Jiang
{"title":"卤素键电荷转移配合物介导的非活性烯烃的光化学全氟烷基化反应","authors":"Huangbin Sun , Chang Huang , Xueting Bin , Fuzhi Cui , Guofang Jiang","doi":"10.1039/d3qo00304c","DOIUrl":null,"url":null,"abstract":"<div><p>We describe a catalyst-free visible-light mediated akynylperfluoroalkylation of unactive alkenes with perfluoroalkyl iodides, which provides a series of α-perfluoroalkyl-β-alkynyl ketone derivatives. This new synthetic protocol is enabled by a charge-transfer complex, which is a compound of a 1,4-enynol anion and an enolate ion of acetone as the electron donor and perfluoroalkyl iodides as the electron acceptor. Excellent functional group compatibility and chemoselectivity render this method suitable for fluoroalkylation of pharmaceutically relevant molecules, featuring a broad substrate scope, scalability and significant characteristics of green chemistry, further demonstrating the flexibility and potential for the synthesis of the mentioned compounds.</p></div>","PeriodicalId":94379,"journal":{"name":"Organic chemistry frontiers : an international journal of organic chemistry","volume":"10 9","pages":"Pages 2332-2339"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Photochemical akynylperfluoroalkylation of unactive alkenes mediated by halogen-bonded charge-transfer complexes†\",\"authors\":\"Huangbin Sun , Chang Huang , Xueting Bin , Fuzhi Cui , Guofang Jiang\",\"doi\":\"10.1039/d3qo00304c\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>We describe a catalyst-free visible-light mediated akynylperfluoroalkylation of unactive alkenes with perfluoroalkyl iodides, which provides a series of α-perfluoroalkyl-β-alkynyl ketone derivatives. This new synthetic protocol is enabled by a charge-transfer complex, which is a compound of a 1,4-enynol anion and an enolate ion of acetone as the electron donor and perfluoroalkyl iodides as the electron acceptor. Excellent functional group compatibility and chemoselectivity render this method suitable for fluoroalkylation of pharmaceutically relevant molecules, featuring a broad substrate scope, scalability and significant characteristics of green chemistry, further demonstrating the flexibility and potential for the synthesis of the mentioned compounds.</p></div>\",\"PeriodicalId\":94379,\"journal\":{\"name\":\"Organic chemistry frontiers : an international journal of organic chemistry\",\"volume\":\"10 9\",\"pages\":\"Pages 2332-2339\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic chemistry frontiers : an international journal of organic chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S2052411023000275\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic chemistry frontiers : an international journal of organic chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2052411023000275","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Photochemical akynylperfluoroalkylation of unactive alkenes mediated by halogen-bonded charge-transfer complexes†
We describe a catalyst-free visible-light mediated akynylperfluoroalkylation of unactive alkenes with perfluoroalkyl iodides, which provides a series of α-perfluoroalkyl-β-alkynyl ketone derivatives. This new synthetic protocol is enabled by a charge-transfer complex, which is a compound of a 1,4-enynol anion and an enolate ion of acetone as the electron donor and perfluoroalkyl iodides as the electron acceptor. Excellent functional group compatibility and chemoselectivity render this method suitable for fluoroalkylation of pharmaceutically relevant molecules, featuring a broad substrate scope, scalability and significant characteristics of green chemistry, further demonstrating the flexibility and potential for the synthesis of the mentioned compounds.