{"title":"照亮对映选择性烷基-烷基偶联","authors":"Weisai Zu, Xinlong Luo, Haohua Huo","doi":"10.1038/s41929-025-01327-4","DOIUrl":null,"url":null,"abstract":"The catalytic enantioselective formation of alkyl−alkyl bonds from simple feedstock chemicals remains a formidable challenge in organic synthesis. Now, an enantioconvergent approach that couples styrenyl aziridines with unactivated olefins using a chiral nickel catalyst and visible light has been developed.","PeriodicalId":18845,"journal":{"name":"Nature Catalysis","volume":"33 1","pages":"289-290"},"PeriodicalIF":42.8000,"publicationDate":"2025-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Illuminating enantioselective alkyl−alkyl coupling\",\"authors\":\"Weisai Zu, Xinlong Luo, Haohua Huo\",\"doi\":\"10.1038/s41929-025-01327-4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The catalytic enantioselective formation of alkyl−alkyl bonds from simple feedstock chemicals remains a formidable challenge in organic synthesis. Now, an enantioconvergent approach that couples styrenyl aziridines with unactivated olefins using a chiral nickel catalyst and visible light has been developed.\",\"PeriodicalId\":18845,\"journal\":{\"name\":\"Nature Catalysis\",\"volume\":\"33 1\",\"pages\":\"289-290\"},\"PeriodicalIF\":42.8000,\"publicationDate\":\"2025-04-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nature Catalysis\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1038/s41929-025-01327-4\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Catalysis","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1038/s41929-025-01327-4","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
The catalytic enantioselective formation of alkyl−alkyl bonds from simple feedstock chemicals remains a formidable challenge in organic synthesis. Now, an enantioconvergent approach that couples styrenyl aziridines with unactivated olefins using a chiral nickel catalyst and visible light has been developed.
期刊介绍:
Nature Catalysis serves as a platform for researchers across chemistry and related fields, focusing on homogeneous catalysis, heterogeneous catalysis, and biocatalysts, encompassing both fundamental and applied studies. With a particular emphasis on advancing sustainable industries and processes, the journal provides comprehensive coverage of catalysis research, appealing to scientists, engineers, and researchers in academia and industry.
Maintaining the high standards of the Nature brand, Nature Catalysis boasts a dedicated team of professional editors, rigorous peer-review processes, and swift publication times, ensuring editorial independence and quality. The journal publishes work spanning heterogeneous catalysis, homogeneous catalysis, and biocatalysis, covering areas such as catalytic synthesis, mechanisms, characterization, computational studies, nanoparticle catalysis, electrocatalysis, photocatalysis, environmental catalysis, asymmetric catalysis, and various forms of organocatalysis.