{"title":"亚砜亚胺的无过渡金属脱羧酰化:N-(邻氨基苯甲酰)亚砜亚胺的有效途径","authors":"Meng Ding, Qingle Zeng","doi":"10.1016/j.tet.2025.134867","DOIUrl":null,"url":null,"abstract":"<div><div>A transition-metal-free decarboxylative acylation strategy for constructing C–N bonds in sulfoximines and isatoic anhydrides is reported. This method enables the synthesis of 26 N-(ortho-aminobenzoyl)sulfoximines in 52 %–82 % yields, featuring gram-scale feasibility and versatile post-modifications for potential bioactive derivatives.</div></div>","PeriodicalId":437,"journal":{"name":"Tetrahedron","volume":"185 ","pages":"Article 134867"},"PeriodicalIF":2.2000,"publicationDate":"2025-07-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Transition-metal-free decarboxylative acylation of sulfoximines: An efficient route to N-(ortho-aminobenzoyl)sulfoximines\",\"authors\":\"Meng Ding, Qingle Zeng\",\"doi\":\"10.1016/j.tet.2025.134867\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A transition-metal-free decarboxylative acylation strategy for constructing C–N bonds in sulfoximines and isatoic anhydrides is reported. This method enables the synthesis of 26 N-(ortho-aminobenzoyl)sulfoximines in 52 %–82 % yields, featuring gram-scale feasibility and versatile post-modifications for potential bioactive derivatives.</div></div>\",\"PeriodicalId\":437,\"journal\":{\"name\":\"Tetrahedron\",\"volume\":\"185 \",\"pages\":\"Article 134867\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2025-07-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Tetrahedron\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0040402025004235\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tetrahedron","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0040402025004235","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Transition-metal-free decarboxylative acylation of sulfoximines: An efficient route to N-(ortho-aminobenzoyl)sulfoximines
A transition-metal-free decarboxylative acylation strategy for constructing C–N bonds in sulfoximines and isatoic anhydrides is reported. This method enables the synthesis of 26 N-(ortho-aminobenzoyl)sulfoximines in 52 %–82 % yields, featuring gram-scale feasibility and versatile post-modifications for potential bioactive derivatives.
期刊介绍:
Tetrahedron publishes full accounts of research having outstanding significance in the broad field of organic chemistry and its related disciplines, such as organic materials and bio-organic chemistry.
Regular papers in Tetrahedron are expected to represent detailed accounts of an original study having substantially greater scope and details than that found in a communication, as published in Tetrahedron Letters.
Tetrahedron also publishes thematic collections of papers as special issues and ''Reports'', commissioned in-depth reviews providing a comprehensive overview of a research area.