{"title":"儿茶酚催化的烷基硼酸与醛和胺的光催化羰基化四组分反应","authors":"Qiangwei Li , Le-Cheng Wang , Xiao-Feng Wu","doi":"10.1039/d5gc02383a","DOIUrl":null,"url":null,"abstract":"<div><div>Carbonylation reactions employing CO as an easily accessible Cl source have emerged as one of the most powerful tools for constructing carbonyl-containing compounds from readily available starting materials. Despite the impressive achievements on carbonylative transformations, a fundamental limitation of these approaches lies in their reliance on transition metal catalysis or a stoichiometric amount of activating reagents. Herein, we report the first photo-induced catechol-catalyzed four-component carbonylation reaction of alkylboronic acids with aldehydes and amines. A range of valuable substituted α-amino ketones was produced in moderate to good yields.</div></div>","PeriodicalId":78,"journal":{"name":"Green Chemistry","volume":"27 28","pages":"Pages 8492-8497"},"PeriodicalIF":9.2000,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A catechol-catalyzed photocatalytic carbonylative four-component reaction of alkylboronic acids with aldehydes and amines†\",\"authors\":\"Qiangwei Li , Le-Cheng Wang , Xiao-Feng Wu\",\"doi\":\"10.1039/d5gc02383a\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Carbonylation reactions employing CO as an easily accessible Cl source have emerged as one of the most powerful tools for constructing carbonyl-containing compounds from readily available starting materials. Despite the impressive achievements on carbonylative transformations, a fundamental limitation of these approaches lies in their reliance on transition metal catalysis or a stoichiometric amount of activating reagents. Herein, we report the first photo-induced catechol-catalyzed four-component carbonylation reaction of alkylboronic acids with aldehydes and amines. A range of valuable substituted α-amino ketones was produced in moderate to good yields.</div></div>\",\"PeriodicalId\":78,\"journal\":{\"name\":\"Green Chemistry\",\"volume\":\"27 28\",\"pages\":\"Pages 8492-8497\"},\"PeriodicalIF\":9.2000,\"publicationDate\":\"2025-04-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Green Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1463926225005370\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Green Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1463926225005370","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
A catechol-catalyzed photocatalytic carbonylative four-component reaction of alkylboronic acids with aldehydes and amines†
Carbonylation reactions employing CO as an easily accessible Cl source have emerged as one of the most powerful tools for constructing carbonyl-containing compounds from readily available starting materials. Despite the impressive achievements on carbonylative transformations, a fundamental limitation of these approaches lies in their reliance on transition metal catalysis or a stoichiometric amount of activating reagents. Herein, we report the first photo-induced catechol-catalyzed four-component carbonylation reaction of alkylboronic acids with aldehydes and amines. A range of valuable substituted α-amino ketones was produced in moderate to good yields.
期刊介绍:
Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.