Qing He , Yu-Qi Xiang , Rui Zhou , Bin Liu , Rong-Hua Wang , Xiang-Kai Kong , Song Bai , Miao Li , Guang-Jun Yang , Gao-Feng Zhu
{"title":"低负荷[3 + 3]苯并环法制备多功能化三氟甲基芳烃的无金属催化新结构","authors":"Qing He , Yu-Qi Xiang , Rui Zhou , Bin Liu , Rong-Hua Wang , Xiang-Kai Kong , Song Bai , Miao Li , Guang-Jun Yang , Gao-Feng Zhu","doi":"10.1039/d5qo00013k","DOIUrl":null,"url":null,"abstract":"<div><div>A low catalyst loading and transition metal-free benzannulation of β,γ-alkynyl-α-keto esters and CF<sub>3</sub>-alkenes has been developed through Michael-triggered [3 + 3] annulation. The newly developed methodology provides highly efficient and rapid access to a variety of multi-functionalised trifluoromethylarene derivatives in generally good to excellent yields. The late-stage functionalisation of some natural products and bioactive molecules and the gram-scale reaction as well as transformation of the products indicate that the present protocol has significant practical value and reliability.</div></div>","PeriodicalId":94379,"journal":{"name":"Organic chemistry frontiers : an international journal of organic chemistry","volume":"12 8","pages":"Pages 2670-2675"},"PeriodicalIF":0.0000,"publicationDate":"2025-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Metal-free catalytic de novo construction of multi-functionalized trifluoromethylarenes through [3 + 3] benzannulation at low catalyst loadings†\",\"authors\":\"Qing He , Yu-Qi Xiang , Rui Zhou , Bin Liu , Rong-Hua Wang , Xiang-Kai Kong , Song Bai , Miao Li , Guang-Jun Yang , Gao-Feng Zhu\",\"doi\":\"10.1039/d5qo00013k\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A low catalyst loading and transition metal-free benzannulation of β,γ-alkynyl-α-keto esters and CF<sub>3</sub>-alkenes has been developed through Michael-triggered [3 + 3] annulation. The newly developed methodology provides highly efficient and rapid access to a variety of multi-functionalised trifluoromethylarene derivatives in generally good to excellent yields. The late-stage functionalisation of some natural products and bioactive molecules and the gram-scale reaction as well as transformation of the products indicate that the present protocol has significant practical value and reliability.</div></div>\",\"PeriodicalId\":94379,\"journal\":{\"name\":\"Organic chemistry frontiers : an international journal of organic chemistry\",\"volume\":\"12 8\",\"pages\":\"Pages 2670-2675\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-02-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"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/S2052412925001081\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/2/25 0:00:00\",\"PubModel\":\"Epub\",\"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/S2052412925001081","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/25 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
Metal-free catalytic de novo construction of multi-functionalized trifluoromethylarenes through [3 + 3] benzannulation at low catalyst loadings†
A low catalyst loading and transition metal-free benzannulation of β,γ-alkynyl-α-keto esters and CF3-alkenes has been developed through Michael-triggered [3 + 3] annulation. The newly developed methodology provides highly efficient and rapid access to a variety of multi-functionalised trifluoromethylarene derivatives in generally good to excellent yields. The late-stage functionalisation of some natural products and bioactive molecules and the gram-scale reaction as well as transformation of the products indicate that the present protocol has significant practical value and reliability.