{"title":"无过渡金属合成苯并噻吩吡啶、苯并硒代吡啶、苯并telluropyridine及相关类似物的统一策略","authors":"Zhaoyue Wen, Jianlian Wu, Chun Wang, Bingjie Shen, Mingyue Fu, Xinni Zheng, Cheng Lu, Wei Chen, Tie-Gen Chen","doi":"10.1021/acs.orglett.5c01557","DOIUrl":null,"url":null,"abstract":"A transition-metal-free, unified synthetic approach has been developed for the efficient construction of benzothienopyridines, benzoselenopyridines, and benzotelluropyridines. This versatile methodology facilitates the formation of C–S, C–Se, and C–Te bonds through the cyclization reaction of readily available dihalogenated pyridyl biaryls with chalcogen sources (thiourea, elemental sulfur, selenium, or tellurium). Significantly, the derivatized products exhibit promising potential as building blocks for benzochalcogenophene-fused pyridine architectures and functional materials for organic optoelectronic applications, particularly in organic light-emitting diodes.","PeriodicalId":54,"journal":{"name":"Organic Letters","volume":"47 1","pages":""},"PeriodicalIF":5.0000,"publicationDate":"2025-06-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Unified Strategy for Transition-Metal-Free Synthesis of Benzothienopyridines, Benzoselenopyridines, and Benzotelluropyridines and Related Analogues\",\"authors\":\"Zhaoyue Wen, Jianlian Wu, Chun Wang, Bingjie Shen, Mingyue Fu, Xinni Zheng, Cheng Lu, Wei Chen, Tie-Gen Chen\",\"doi\":\"10.1021/acs.orglett.5c01557\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A transition-metal-free, unified synthetic approach has been developed for the efficient construction of benzothienopyridines, benzoselenopyridines, and benzotelluropyridines. This versatile methodology facilitates the formation of C–S, C–Se, and C–Te bonds through the cyclization reaction of readily available dihalogenated pyridyl biaryls with chalcogen sources (thiourea, elemental sulfur, selenium, or tellurium). Significantly, the derivatized products exhibit promising potential as building blocks for benzochalcogenophene-fused pyridine architectures and functional materials for organic optoelectronic applications, particularly in organic light-emitting diodes.\",\"PeriodicalId\":54,\"journal\":{\"name\":\"Organic Letters\",\"volume\":\"47 1\",\"pages\":\"\"},\"PeriodicalIF\":5.0000,\"publicationDate\":\"2025-06-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic Letters\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.orglett.5c01557\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic Letters","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.orglett.5c01557","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
A Unified Strategy for Transition-Metal-Free Synthesis of Benzothienopyridines, Benzoselenopyridines, and Benzotelluropyridines and Related Analogues
A transition-metal-free, unified synthetic approach has been developed for the efficient construction of benzothienopyridines, benzoselenopyridines, and benzotelluropyridines. This versatile methodology facilitates the formation of C–S, C–Se, and C–Te bonds through the cyclization reaction of readily available dihalogenated pyridyl biaryls with chalcogen sources (thiourea, elemental sulfur, selenium, or tellurium). Significantly, the derivatized products exhibit promising potential as building blocks for benzochalcogenophene-fused pyridine architectures and functional materials for organic optoelectronic applications, particularly in organic light-emitting diodes.
期刊介绍:
Organic Letters invites original reports of fundamental research in all branches of the theory and practice of organic, physical organic, organometallic,medicinal, and bioorganic chemistry. Organic Letters provides rapid disclosure of the key elements of significant studies that are of interest to a large portion of the organic community. In selecting manuscripts for publication, the Editors place emphasis on the originality, quality and wide interest of the work. Authors should provide enough background information to place the new disclosure in context and to justify the rapid publication format. Back-to-back Letters will be considered. Full details should be reserved for an Article, which should appear in due course.