{"title":"Co(III)催化2-烯基吡啶与2-乙烯基氮基吡啶的烯丙基化反应:得到1,4-二烯。","authors":"Hong Zeng, Zhong-Xia Wang","doi":"10.1039/d5ob01343g","DOIUrl":null,"url":null,"abstract":"<p><p>A Cp*(CO)CoI<sub>2</sub>-catalyzed C-H allylation of 2-alkenylpyridines with 2-vinylaziridines is described. This method provides efficient access to synthetically useful 1,4-diene skeletons. The approach features a simple reaction system, nitrogen-containing group retainment, atom economy, short reaction times, wide substrate scope and good tolerance towards functional groups.</p>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":" ","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2025-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Co(III)-catalyzed allylation reaction of 2-alkenylpyridines with 2-vinylaziridines: access to 1,4-dienes.\",\"authors\":\"Hong Zeng, Zhong-Xia Wang\",\"doi\":\"10.1039/d5ob01343g\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>A Cp*(CO)CoI<sub>2</sub>-catalyzed C-H allylation of 2-alkenylpyridines with 2-vinylaziridines is described. This method provides efficient access to synthetically useful 1,4-diene skeletons. The approach features a simple reaction system, nitrogen-containing group retainment, atom economy, short reaction times, wide substrate scope and good tolerance towards functional groups.</p>\",\"PeriodicalId\":96,\"journal\":{\"name\":\"Organic & Biomolecular Chemistry\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-10-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic & Biomolecular Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d5ob01343g\",\"RegionNum\":3,\"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 & Biomolecular Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5ob01343g","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Co(III)-catalyzed allylation reaction of 2-alkenylpyridines with 2-vinylaziridines: access to 1,4-dienes.
A Cp*(CO)CoI2-catalyzed C-H allylation of 2-alkenylpyridines with 2-vinylaziridines is described. This method provides efficient access to synthetically useful 1,4-diene skeletons. The approach features a simple reaction system, nitrogen-containing group retainment, atom economy, short reaction times, wide substrate scope and good tolerance towards functional groups.
期刊介绍:
Organic & Biomolecular Chemistry is an international journal using integrated research in chemistry-organic chemistry. Founded in 2003 by the Royal Society of Chemistry, the journal is published in Semimonthly issues and has been indexed by SCIE, a leading international database. The journal focuses on the key research and cutting-edge progress in the field of chemistry-organic chemistry, publishes and reports the research results in this field in a timely manner, and is committed to becoming a window and platform for rapid academic exchanges among peers in this field. The journal's impact factor in 2023 is 2.9, and its CiteScore is 5.5.