{"title":"苯胺的去芳构化-断裂-芳构化:与宽杂原子亲核试剂合成3,3-二取代吲哚的过程","authors":"Priyankar Jha, Saddam Husen, Sagar Sinha, Ravindra Kumar","doi":"10.1039/d5cc02309b","DOIUrl":null,"url":null,"abstract":"Herein, we report a catalytic, redox-neutral method for the difunctionalization of oxindoles using ketimines derived from anilines and heteronucleophiles. The reaction proceeds through dearomatization-aromatization strategy via tetra-substituted alkene intermediate stabilized by extended resonance, facilitating the selective formation of 3,3-disubstituted oxindoles with wide chemical space in good to high yields.","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":"148 1","pages":""},"PeriodicalIF":4.2000,"publicationDate":"2025-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dearomatization-Scission-Aromatization of Anilines: En route to Synthesis of 3,3-Disubstituted Oxindoles with Wide Heteroatom Nucleophiles\",\"authors\":\"Priyankar Jha, Saddam Husen, Sagar Sinha, Ravindra Kumar\",\"doi\":\"10.1039/d5cc02309b\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Herein, we report a catalytic, redox-neutral method for the difunctionalization of oxindoles using ketimines derived from anilines and heteronucleophiles. The reaction proceeds through dearomatization-aromatization strategy via tetra-substituted alkene intermediate stabilized by extended resonance, facilitating the selective formation of 3,3-disubstituted oxindoles with wide chemical space in good to high yields.\",\"PeriodicalId\":67,\"journal\":{\"name\":\"Chemical Communications\",\"volume\":\"148 1\",\"pages\":\"\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-07-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Communications\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d5cc02309b\",\"RegionNum\":2,\"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":"Chemical Communications","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5cc02309b","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Dearomatization-Scission-Aromatization of Anilines: En route to Synthesis of 3,3-Disubstituted Oxindoles with Wide Heteroatom Nucleophiles
Herein, we report a catalytic, redox-neutral method for the difunctionalization of oxindoles using ketimines derived from anilines and heteronucleophiles. The reaction proceeds through dearomatization-aromatization strategy via tetra-substituted alkene intermediate stabilized by extended resonance, facilitating the selective formation of 3,3-disubstituted oxindoles with wide chemical space in good to high yields.
期刊介绍:
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