{"title":"铜催化环二芳基鎓的双n -芳基化:5h -二苯并[d, f][1,3]二氮卓和苯并[c]喹啉衍生物的合成","authors":"Lianji Zhang, Yujuan Wu, Yuhui Zhao, Cuiping Wang, Wanguo Wei, Zhiqiang Zhang","doi":"10.1002/jhet.4914","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>An efficient access to novel families of 7-membered dibenzodiazepines and 6-membered benzo[<i>c</i>]cinnoline derivatives has been elaborated. The synthetic strategy is based on a copper-catalyzed double <i>N</i>-arylation of cyclic diaryliodoniums with imidamides and 4-substituted 1, 2, 4-triazoline-3, 5-diones (TADs) respectively under ambient reaction conditions. A mechanistic rationale for the double <i>N</i>-arylation is discussed.</p>\n </div>","PeriodicalId":194,"journal":{"name":"Journal of Heterocyclic Chemistry","volume":"61 12","pages":"1942-1953"},"PeriodicalIF":2.0000,"publicationDate":"2024-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Practical Copper-Catalyzed Double N-Arylation of Cyclic Diaryliodoniums: Synthesis of 5H-Dibenzo[d, f][1,3]Diazepine, and Benzo[c]Cinnoline Derivatives\",\"authors\":\"Lianji Zhang, Yujuan Wu, Yuhui Zhao, Cuiping Wang, Wanguo Wei, Zhiqiang Zhang\",\"doi\":\"10.1002/jhet.4914\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <p>An efficient access to novel families of 7-membered dibenzodiazepines and 6-membered benzo[<i>c</i>]cinnoline derivatives has been elaborated. The synthetic strategy is based on a copper-catalyzed double <i>N</i>-arylation of cyclic diaryliodoniums with imidamides and 4-substituted 1, 2, 4-triazoline-3, 5-diones (TADs) respectively under ambient reaction conditions. A mechanistic rationale for the double <i>N</i>-arylation is discussed.</p>\\n </div>\",\"PeriodicalId\":194,\"journal\":{\"name\":\"Journal of Heterocyclic Chemistry\",\"volume\":\"61 12\",\"pages\":\"1942-1953\"},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2024-09-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Heterocyclic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/jhet.4914\",\"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":"Journal of Heterocyclic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jhet.4914","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Practical Copper-Catalyzed Double N-Arylation of Cyclic Diaryliodoniums: Synthesis of 5H-Dibenzo[d, f][1,3]Diazepine, and Benzo[c]Cinnoline Derivatives
An efficient access to novel families of 7-membered dibenzodiazepines and 6-membered benzo[c]cinnoline derivatives has been elaborated. The synthetic strategy is based on a copper-catalyzed double N-arylation of cyclic diaryliodoniums with imidamides and 4-substituted 1, 2, 4-triazoline-3, 5-diones (TADs) respectively under ambient reaction conditions. A mechanistic rationale for the double N-arylation is discussed.
期刊介绍:
The Journal of Heterocyclic Chemistry is interested in publishing research on all aspects of heterocyclic chemistry, especially development and application of efficient synthetic methodologies and strategies for the synthesis of various heterocyclic compounds. In addition, Journal of Heterocyclic Chemistry promotes research in other areas that contribute to heterocyclic synthesis/application, such as synthesis design, reaction techniques, flow chemistry and continuous processing, multiphase catalysis, green chemistry, catalyst immobilization and recycling.