{"title":"光照射下铁催化区域选择性α,α-二氯羰基化反应","authors":"Chen Bao, Meng Guan","doi":"10.1016/j.tetlet.2025.155786","DOIUrl":null,"url":null,"abstract":"<div><div>α,α-Dichlorocarbonyl core exhibited unique versatility towards a series of cyclic and acyclic scaffolds. Besides, it is ubiquitous in numerous biologically interesting products. As such, efficient and divergent synthetic methodology for achieving α,α-dichlorocarbonyl structural core under mild conditions attracted tremendous attentions so far. In this paper, an efficient route for the synthesis of α,α-dichlorocarbonyl compounds via an oxidative nucleophilic oxychlorination of alkyne under iron/photo dual catalysis is described under mild conditions.</div></div>","PeriodicalId":438,"journal":{"name":"Tetrahedron Letters","volume":"170 ","pages":"Article 155786"},"PeriodicalIF":1.5000,"publicationDate":"2025-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Iron-catalyzed regioselective α,α-dichlorocarbonylation of alkynes under photo-irradiation\",\"authors\":\"Chen Bao, Meng Guan\",\"doi\":\"10.1016/j.tetlet.2025.155786\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>α,α-Dichlorocarbonyl core exhibited unique versatility towards a series of cyclic and acyclic scaffolds. Besides, it is ubiquitous in numerous biologically interesting products. As such, efficient and divergent synthetic methodology for achieving α,α-dichlorocarbonyl structural core under mild conditions attracted tremendous attentions so far. In this paper, an efficient route for the synthesis of α,α-dichlorocarbonyl compounds via an oxidative nucleophilic oxychlorination of alkyne under iron/photo dual catalysis is described under mild conditions.</div></div>\",\"PeriodicalId\":438,\"journal\":{\"name\":\"Tetrahedron Letters\",\"volume\":\"170 \",\"pages\":\"Article 155786\"},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2025-08-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Tetrahedron Letters\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0040403925003351\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tetrahedron Letters","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0040403925003351","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Iron-catalyzed regioselective α,α-dichlorocarbonylation of alkynes under photo-irradiation
α,α-Dichlorocarbonyl core exhibited unique versatility towards a series of cyclic and acyclic scaffolds. Besides, it is ubiquitous in numerous biologically interesting products. As such, efficient and divergent synthetic methodology for achieving α,α-dichlorocarbonyl structural core under mild conditions attracted tremendous attentions so far. In this paper, an efficient route for the synthesis of α,α-dichlorocarbonyl compounds via an oxidative nucleophilic oxychlorination of alkyne under iron/photo dual catalysis is described under mild conditions.
期刊介绍:
Tetrahedron Letters provides maximum dissemination of outstanding developments in organic chemistry. The journal is published weekly and covers developments in techniques, structures, methods and conclusions in experimental and theoretical organic chemistry. Rapid publication of timely and significant research results enables researchers from all over the world to transmit quickly their new contributions to large, international audiences.