{"title":"A practical synthesis of functionalized pyrazoles promoted by a polyoxomolybdate-based iron catalyst","authors":"Lianji Zhang , Yujuan Wu , Cuiping Wang , Wanguo Wei , Zhiqiang Zhang","doi":"10.1080/00397911.2025.2455529","DOIUrl":null,"url":null,"abstract":"<div><div>An efficient synthesis of pyrazole scaffolds from arylsulfonylhydrazines and diketones promoted by a molecular molybdenum oxide catalyst (NH<sub>4</sub>)<sub>3</sub>[FeMo<sub>6</sub>O<sub>18</sub>(OH)<sub>6</sub>] is described. The iron-based polyoxometalate catalyst is heterogeneous, reusable with stable recyclability. Using this method, a wide range of arylsulfonylhydrazines and diketones can undergo smoothly condensation cyclization to produce functionalized pyrazoles in high yields.</div></div>","PeriodicalId":22119,"journal":{"name":"Synthetic Communications","volume":"55 5","pages":"Pages 373-380"},"PeriodicalIF":1.8000,"publicationDate":"2025-01-24","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/S0039791125000098","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
An efficient synthesis of pyrazole scaffolds from arylsulfonylhydrazines and diketones promoted by a molecular molybdenum oxide catalyst (NH4)3[FeMo6O18(OH)6] is described. The iron-based polyoxometalate catalyst is heterogeneous, reusable with stable recyclability. Using this method, a wide range of arylsulfonylhydrazines and diketones can undergo smoothly condensation cyclization to produce functionalized pyrazoles in high yields.
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.