{"title":"Manganese(I)-NNSe Pincer Complex Mediated Dehydrogenative Cyclization to Synthesize 2-Aryl-2,3-dihydroquinolin-4(1H)-ones","authors":"Suman Mahala, Sohan Singh, Palak Rakesh, Nattamai Bhuvanesh, Hemant Joshi","doi":"10.1021/acs.joc.4c02731","DOIUrl":null,"url":null,"abstract":"A catalytic one-pot cascade dehydrogenative cyclization of 1-(2-aminophenyl)ethanone using primary alcohols is presented. The reaction is catalyzed by an earth-abundant manganese pincer complex of NNSe ligand, without any solvent, additives, base, or hydrogen acceptor, liberating dihydrogen and water as the only byproducts. Compared to an earlier reported four-step dehydrogenative coupling protocol, only a single step is required to synthesize 2-aryl-2,3-dihydroquinolin-4(1<i>H</i>)-ones.","PeriodicalId":57,"journal":{"name":"Journal of Organic Chemistry","volume":"210 1","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2025-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Organic Chemistry","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1021/acs.joc.4c02731","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0
Abstract
A catalytic one-pot cascade dehydrogenative cyclization of 1-(2-aminophenyl)ethanone using primary alcohols is presented. The reaction is catalyzed by an earth-abundant manganese pincer complex of NNSe ligand, without any solvent, additives, base, or hydrogen acceptor, liberating dihydrogen and water as the only byproducts. Compared to an earlier reported four-step dehydrogenative coupling protocol, only a single step is required to synthesize 2-aryl-2,3-dihydroquinolin-4(1H)-ones.
期刊介绍:
Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.