Jiaqi Pei, Tiantian Tang, Jianing Zhang, Yunlong Qin, Pengfei Cheng and Qilin Wang
{"title":"异喹啉鎓盐的非对映选择性脱芳香双官能化,获得桥联四氢异喹啉†。","authors":"Jiaqi Pei, Tiantian Tang, Jianing Zhang, Yunlong Qin, Pengfei Cheng and Qilin Wang","doi":"10.1039/D4NJ02968B","DOIUrl":null,"url":null,"abstract":"<p >Herein, we report a diastereoselective dearomative bifunctionalization strategy of using isoquinolinium salts to access bridged tetrahydroisoquinolines. The strategy relies on the strategic use of allenes and amines as reaction partners to generate binucleophilic species <em>in situ</em> for subsequent dearomatization.</p>","PeriodicalId":95,"journal":{"name":"New Journal of Chemistry","volume":" 37","pages":" 16151-16154"},"PeriodicalIF":2.5000,"publicationDate":"2024-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Diastereoselective dearomative bifunctionalization of isoquinolinium salts to access bridged tetrahydroisoquinolines†\",\"authors\":\"Jiaqi Pei, Tiantian Tang, Jianing Zhang, Yunlong Qin, Pengfei Cheng and Qilin Wang\",\"doi\":\"10.1039/D4NJ02968B\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Herein, we report a diastereoselective dearomative bifunctionalization strategy of using isoquinolinium salts to access bridged tetrahydroisoquinolines. The strategy relies on the strategic use of allenes and amines as reaction partners to generate binucleophilic species <em>in situ</em> for subsequent dearomatization.</p>\",\"PeriodicalId\":95,\"journal\":{\"name\":\"New Journal of Chemistry\",\"volume\":\" 37\",\"pages\":\" 16151-16154\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2024-09-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"New Journal of Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/nj/d4nj02968b\",\"RegionNum\":3,\"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":"New Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/nj/d4nj02968b","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Diastereoselective dearomative bifunctionalization of isoquinolinium salts to access bridged tetrahydroisoquinolines†
Herein, we report a diastereoselective dearomative bifunctionalization strategy of using isoquinolinium salts to access bridged tetrahydroisoquinolines. The strategy relies on the strategic use of allenes and amines as reaction partners to generate binucleophilic species in situ for subsequent dearomatization.