{"title":"钯催化的 gem-DFCP 与吡喃酮/吡啶酮的开环/脱氟偶联","authors":"Ling-Juan Tang , Shun-Jun Ji , Zhong-Jian Cai","doi":"10.1016/j.tet.2024.134271","DOIUrl":null,"url":null,"abstract":"<div><p>The monofluoroalkenes are found widespread applications in areas such as bioactive molecules, materials science and synthetic organic chemistry, therefore, investigating efficient methodologies to construct monofluoroalkenes is still in demand. In this paper, we reported an efficient synthesis of monofluoroalkenyl substituted pyranones/pyridones by using the <em>gem</em>-difluorocyclopropanes (<em>gem</em>-DFCPs) as monofluoroalkenyl precursors. In the presence of Palladium catalyst, the monofluoroalkenyl group was introduced into the C3 positions of pyranones/pyridones successfully. The reaction was featured with high regioselectivity, mild conditions, broad substrate scope, easy to scale up synthesis, which provided a novel avenue for the late-stagy modification of pyranones/pyridones.</p></div>","PeriodicalId":437,"journal":{"name":"Tetrahedron","volume":null,"pages":null},"PeriodicalIF":2.1000,"publicationDate":"2024-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Palladium-catalyzed ring-opening/defluorinative coupling of gem-DFCPs with pyranones/pyridones\",\"authors\":\"Ling-Juan Tang , Shun-Jun Ji , Zhong-Jian Cai\",\"doi\":\"10.1016/j.tet.2024.134271\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The monofluoroalkenes are found widespread applications in areas such as bioactive molecules, materials science and synthetic organic chemistry, therefore, investigating efficient methodologies to construct monofluoroalkenes is still in demand. In this paper, we reported an efficient synthesis of monofluoroalkenyl substituted pyranones/pyridones by using the <em>gem</em>-difluorocyclopropanes (<em>gem</em>-DFCPs) as monofluoroalkenyl precursors. In the presence of Palladium catalyst, the monofluoroalkenyl group was introduced into the C3 positions of pyranones/pyridones successfully. The reaction was featured with high regioselectivity, mild conditions, broad substrate scope, easy to scale up synthesis, which provided a novel avenue for the late-stagy modification of pyranones/pyridones.</p></div>\",\"PeriodicalId\":437,\"journal\":{\"name\":\"Tetrahedron\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2024-09-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Tetrahedron\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0040402024004526\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tetrahedron","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0040402024004526","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Palladium-catalyzed ring-opening/defluorinative coupling of gem-DFCPs with pyranones/pyridones
The monofluoroalkenes are found widespread applications in areas such as bioactive molecules, materials science and synthetic organic chemistry, therefore, investigating efficient methodologies to construct monofluoroalkenes is still in demand. In this paper, we reported an efficient synthesis of monofluoroalkenyl substituted pyranones/pyridones by using the gem-difluorocyclopropanes (gem-DFCPs) as monofluoroalkenyl precursors. In the presence of Palladium catalyst, the monofluoroalkenyl group was introduced into the C3 positions of pyranones/pyridones successfully. The reaction was featured with high regioselectivity, mild conditions, broad substrate scope, easy to scale up synthesis, which provided a novel avenue for the late-stagy modification of pyranones/pyridones.
期刊介绍:
Tetrahedron publishes full accounts of research having outstanding significance in the broad field of organic chemistry and its related disciplines, such as organic materials and bio-organic chemistry.
Regular papers in Tetrahedron are expected to represent detailed accounts of an original study having substantially greater scope and details than that found in a communication, as published in Tetrahedron Letters.
Tetrahedron also publishes thematic collections of papers as special issues and ''Reports'', commissioned in-depth reviews providing a comprehensive overview of a research area.