Shan-Shan Zhang, Rui-Xiang Wang, Qing Gu, Shu-Li You
{"title":"磷催化的苯并咪唑与环丙烯酮的不对称[3+2]萃取反应","authors":"Shan-Shan Zhang, Rui-Xiang Wang, Qing Gu, Shu-Li You","doi":"10.31635/ccschem.024.202403981","DOIUrl":null,"url":null,"abstract":"A phosphine-catalyzed intermolecular asymmetric dearomatization reaction of benzimidazoles with cyclopropenones has been developed. In the presence of 5 mol% of commercially available chiral phosphine catalyst, the dearomative [3+2] annulation reaction proceeds smoothly to afford the corresponding dearomatized heterocycles in excellent yields (up to 98%) and enantioselectivity (up to 99% ee). Meanwhile, this reaction features mild reaction conditions, excellent functional group tolerance, and the compatibility with gram-scale synthesis.\n<figure><img alt=\"\" data-lg-src=\"/cms/asset/9b358c8c-9b58-4d0e-8607-0d68e6825e91/keyimage.jpg\" data-src=\"/cms/asset/8c327161-9011-403d-8fed-03672e952168/keyimage.jpg\" src=\"/specs/ux3/releasedAssets/images/loader-7e60691fbe777356dc81ff6d223a82a6.gif\"/><ul>\n<li>Download figure</li>\n<li>Download PowerPoint</li>\n</ul>\n</figure>","PeriodicalId":9810,"journal":{"name":"CCS Chemistry","volume":null,"pages":null},"PeriodicalIF":9.4000,"publicationDate":"2024-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Phosphine-Catalyzed Asymmetric Dearomative [3+2] Annulation Reaction of Benzimidazoles with Cyclopropenones\",\"authors\":\"Shan-Shan Zhang, Rui-Xiang Wang, Qing Gu, Shu-Li You\",\"doi\":\"10.31635/ccschem.024.202403981\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A phosphine-catalyzed intermolecular asymmetric dearomatization reaction of benzimidazoles with cyclopropenones has been developed. In the presence of 5 mol% of commercially available chiral phosphine catalyst, the dearomative [3+2] annulation reaction proceeds smoothly to afford the corresponding dearomatized heterocycles in excellent yields (up to 98%) and enantioselectivity (up to 99% ee). Meanwhile, this reaction features mild reaction conditions, excellent functional group tolerance, and the compatibility with gram-scale synthesis.\\n<figure><img alt=\\\"\\\" data-lg-src=\\\"/cms/asset/9b358c8c-9b58-4d0e-8607-0d68e6825e91/keyimage.jpg\\\" data-src=\\\"/cms/asset/8c327161-9011-403d-8fed-03672e952168/keyimage.jpg\\\" src=\\\"/specs/ux3/releasedAssets/images/loader-7e60691fbe777356dc81ff6d223a82a6.gif\\\"/><ul>\\n<li>Download figure</li>\\n<li>Download PowerPoint</li>\\n</ul>\\n</figure>\",\"PeriodicalId\":9810,\"journal\":{\"name\":\"CCS Chemistry\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":9.4000,\"publicationDate\":\"2024-03-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"CCS Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.31635/ccschem.024.202403981\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"CCS Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31635/ccschem.024.202403981","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Phosphine-Catalyzed Asymmetric Dearomative [3+2] Annulation Reaction of Benzimidazoles with Cyclopropenones
A phosphine-catalyzed intermolecular asymmetric dearomatization reaction of benzimidazoles with cyclopropenones has been developed. In the presence of 5 mol% of commercially available chiral phosphine catalyst, the dearomative [3+2] annulation reaction proceeds smoothly to afford the corresponding dearomatized heterocycles in excellent yields (up to 98%) and enantioselectivity (up to 99% ee). Meanwhile, this reaction features mild reaction conditions, excellent functional group tolerance, and the compatibility with gram-scale synthesis.
期刊介绍:
CCS Chemistry, the flagship publication of the Chinese Chemical Society, stands as a leading international chemistry journal based in China. With a commitment to global outreach in both contributions and readership, the journal operates on a fully Open Access model, eliminating subscription fees for contributing authors. Issued monthly, all articles are published online promptly upon reaching final publishable form. Additionally, authors have the option to expedite the posting process through Immediate Online Accepted Article posting, making a PDF of their accepted article available online upon journal acceptance.