{"title":"合成化学中的多任务卤代烃","authors":"","doi":"10.1016/j.tetlet.2024.155229","DOIUrl":null,"url":null,"abstract":"<div><p>Haloalkynes that could be accessed from diverse precursors, are versatile in synthetic chemistry as alkynylation and/or halogenation reagents, enabling concise and divergent delivery of functional molecules in selective manners. Recently, additional reactivity and substrate scope of haloalkynes, was also developed, facilitating expedient delivery of fused heterocycles.</p></div>","PeriodicalId":438,"journal":{"name":"Tetrahedron Letters","volume":null,"pages":null},"PeriodicalIF":1.5000,"publicationDate":"2024-07-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Multitasking haloalkynes in synthetic chemistry\",\"authors\":\"\",\"doi\":\"10.1016/j.tetlet.2024.155229\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Haloalkynes that could be accessed from diverse precursors, are versatile in synthetic chemistry as alkynylation and/or halogenation reagents, enabling concise and divergent delivery of functional molecules in selective manners. Recently, additional reactivity and substrate scope of haloalkynes, was also developed, facilitating expedient delivery of fused heterocycles.</p></div>\",\"PeriodicalId\":438,\"journal\":{\"name\":\"Tetrahedron Letters\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2024-07-31\",\"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/S0040403924003241\",\"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/S0040403924003241","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Haloalkynes that could be accessed from diverse precursors, are versatile in synthetic chemistry as alkynylation and/or halogenation reagents, enabling concise and divergent delivery of functional molecules in selective manners. Recently, additional reactivity and substrate scope of haloalkynes, was also developed, facilitating expedient delivery of fused heterocycles.
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.