{"title":"内页图片","authors":"","doi":"10.1002/cjoc.70182","DOIUrl":null,"url":null,"abstract":"<p>A new palladium-catalyzed aminocarbonylative [3+2+1]/[4+2] heteroannulation of allylamines with CO and 4-en-1-yn-3-yl acetates for the synthesis of 1,7,8,8a-tetrahydroisoquinolin-3(2<i>H</i>)-ones has been developed. The method enables the construction of two new six-membered rings in a single reaction step leading to the formation of the isoquino-linone scaffolds. More details are discussed in the article by Li <i>et al</i>. on pages 1819—1823.\n\n <figure>\n <div><picture>\n <source></source></picture><p></p>\n </div>\n </figure></p>","PeriodicalId":151,"journal":{"name":"Chinese Journal of Chemistry","volume":"43 15","pages":""},"PeriodicalIF":5.5000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cjoc.70182","citationCount":"0","resultStr":"{\"title\":\"Inside Cover Picture\",\"authors\":\"\",\"doi\":\"10.1002/cjoc.70182\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>A new palladium-catalyzed aminocarbonylative [3+2+1]/[4+2] heteroannulation of allylamines with CO and 4-en-1-yn-3-yl acetates for the synthesis of 1,7,8,8a-tetrahydroisoquinolin-3(2<i>H</i>)-ones has been developed. The method enables the construction of two new six-membered rings in a single reaction step leading to the formation of the isoquino-linone scaffolds. More details are discussed in the article by Li <i>et al</i>. on pages 1819—1823.\\n\\n <figure>\\n <div><picture>\\n <source></source></picture><p></p>\\n </div>\\n </figure></p>\",\"PeriodicalId\":151,\"journal\":{\"name\":\"Chinese Journal of Chemistry\",\"volume\":\"43 15\",\"pages\":\"\"},\"PeriodicalIF\":5.5000,\"publicationDate\":\"2025-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cjoc.70182\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chinese Journal of Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/cjoc.70182\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinese Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cjoc.70182","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
采用钯催化烯丙胺[3+2+1]/[4+2]杂环反应与CO和4-en-1-yn-3-乙酸酯合成1,7,8,8 A -四氢异喹啉-3(2H)- 1。该方法能够在一个反应步骤中构建两个新的六元环,从而形成异喹诺-烯酮支架。Li等人在1819-1823页的文章中讨论了更多细节。
A new palladium-catalyzed aminocarbonylative [3+2+1]/[4+2] heteroannulation of allylamines with CO and 4-en-1-yn-3-yl acetates for the synthesis of 1,7,8,8a-tetrahydroisoquinolin-3(2H)-ones has been developed. The method enables the construction of two new six-membered rings in a single reaction step leading to the formation of the isoquino-linone scaffolds. More details are discussed in the article by Li et al. on pages 1819—1823.
期刊介绍:
The Chinese Journal of Chemistry is an international forum for peer-reviewed original research results in all fields of chemistry. Founded in 1983 under the name Acta Chimica Sinica English Edition and renamed in 1990 as Chinese Journal of Chemistry, the journal publishes a stimulating mixture of Accounts, Full Papers, Notes and Communications in English.