{"title":"自由基在交叉耦合中保持记忆","authors":"Tao Li, Haohua Huo","doi":"10.1016/j.checat.2025.101439","DOIUrl":null,"url":null,"abstract":"The field of radical chemistry has long faced a fundamental limitation: the instantaneous racemization of free radicals. Reporting in the June 5 issue of <em>Nature</em>, Baran and co-workers have now achieved stereoretentive radical cross-coupling through a unique mechanistic design, opening new synthetic pathways for preparing enantioenriched compounds.","PeriodicalId":53121,"journal":{"name":"Chem Catalysis","volume":"96 1","pages":""},"PeriodicalIF":11.5000,"publicationDate":"2025-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Radicals retain their memory in cross-coupling\",\"authors\":\"Tao Li, Haohua Huo\",\"doi\":\"10.1016/j.checat.2025.101439\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The field of radical chemistry has long faced a fundamental limitation: the instantaneous racemization of free radicals. Reporting in the June 5 issue of <em>Nature</em>, Baran and co-workers have now achieved stereoretentive radical cross-coupling through a unique mechanistic design, opening new synthetic pathways for preparing enantioenriched compounds.\",\"PeriodicalId\":53121,\"journal\":{\"name\":\"Chem Catalysis\",\"volume\":\"96 1\",\"pages\":\"\"},\"PeriodicalIF\":11.5000,\"publicationDate\":\"2025-07-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chem Catalysis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1016/j.checat.2025.101439\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chem Catalysis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.checat.2025.101439","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
The field of radical chemistry has long faced a fundamental limitation: the instantaneous racemization of free radicals. Reporting in the June 5 issue of Nature, Baran and co-workers have now achieved stereoretentive radical cross-coupling through a unique mechanistic design, opening new synthetic pathways for preparing enantioenriched compounds.
期刊介绍:
Chem Catalysis is a monthly journal that publishes innovative research on fundamental and applied catalysis, providing a platform for researchers across chemistry, chemical engineering, and related fields. It serves as a premier resource for scientists and engineers in academia and industry, covering heterogeneous, homogeneous, and biocatalysis. Emphasizing transformative methods and technologies, the journal aims to advance understanding, introduce novel catalysts, and connect fundamental insights to real-world applications for societal benefit.