Yawen Hu (Conceptualization Data curation Formal analysis Investigation Methodology Writing – original draft Writing – review & editing) , Li Xu (Data curation Formal analysis) , Xue Jiang (Data curation Supervision) , Haiyang Guo (Formal analysis Investigation) , Di Wu (Conceptualization Data curation Methodology Writing – review & editing)
{"title":"Recyclable chitosan for copper-catalyzed Ullmann C-N coupling reaction","authors":"Yawen Hu (Conceptualization Data curation Formal analysis Investigation Methodology Writing – original draft Writing – review & editing) , Li Xu (Data curation Formal analysis) , Xue Jiang (Data curation Supervision) , Haiyang Guo (Formal analysis Investigation) , Di Wu (Conceptualization Data curation Methodology Writing – review & editing)","doi":"10.1080/00397911.2025.2548301","DOIUrl":null,"url":null,"abstract":"<div><div>A recyclable ligand chitosan was developed for the copper-catalyzed Ullmann-type cross-coupling reaction of aryl halides with amines. A variety of functionalized (hetero)aryl halides reacted smoothly with pyrazole, imidazole, aliphatic amines and ammonia to provide a wide range of (hetero)aryl amines in good to excellent yields under the catalyst of Cu<sub>2</sub>O/chitosan system. This method has the advantages of wide substrate range, high chemoselectivity, and good functional group compatibility. The ligand is easily recycled and no significant decrease in the catalytic potency after being reused 7 times.</div></div>","PeriodicalId":22119,"journal":{"name":"Synthetic Communications","volume":"55 17","pages":"Pages 1340-1350"},"PeriodicalIF":1.8000,"publicationDate":"2025-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Synthetic Communications","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S0039791125000797","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0
Abstract
A recyclable ligand chitosan was developed for the copper-catalyzed Ullmann-type cross-coupling reaction of aryl halides with amines. A variety of functionalized (hetero)aryl halides reacted smoothly with pyrazole, imidazole, aliphatic amines and ammonia to provide a wide range of (hetero)aryl amines in good to excellent yields under the catalyst of Cu2O/chitosan system. This method has the advantages of wide substrate range, high chemoselectivity, and good functional group compatibility. The ligand is easily recycled and no significant decrease in the catalytic potency after being reused 7 times.
期刊介绍:
Synthetic Communications presents communications describing new methods, reagents, and other synthetic work pertaining to organic chemistry with sufficient experimental detail to permit reported reactions to be repeated by a chemist reasonably skilled in the art. In addition, the Journal features short, focused review articles discussing topics within its remit of synthetic organic chemistry.