{"title":"级联Markovnikov加成/ Lewis酸催化的亚甲叠氮嘧啶和羧酸重排:α-氨基酮的连续流合成","authors":"Bin Pan, Haotian Sun, Feng Li, Qing-Bao Zhang, Shanshan Zhang, Jia-Hao Wang, Meng-Rui Xu, Jing-Tian Ge, Zi-Qing Hu, Shang Lv, Lijuan Feng, Guofu Huang","doi":"10.1039/d5qo00495k","DOIUrl":null,"url":null,"abstract":"α-Amidoketones are essential structural motifs in pharmaceuticals and synthetic chemistry. In this study, we describe a novel synthetic method that involves a cascade addition reaction, followed by a Lewis acid-catalyzed rearrangement of methyleneaziridines and carboxylic acids. Additionally, we developed a high-speed continuous flow synthesis method, allowing the reaction to proceed efficiently within 3.5 minutes. The incorporation of a greener silica gel-packed catalyzed column in this continuous flow system effectively facilitates the rearrangement step, providing a more environmentally friendly approach for synthesizing α-amidoketone compounds.","PeriodicalId":97,"journal":{"name":"Organic Chemistry Frontiers","volume":"71 1","pages":""},"PeriodicalIF":4.6000,"publicationDate":"2025-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Cascade Markovnikov Addition / Lewis Acid-Catalyzed Rearrangement of Methyleneaziridines and Carboxylic Acids: Continuous-Flow Synthesis of α-Amidoketones\",\"authors\":\"Bin Pan, Haotian Sun, Feng Li, Qing-Bao Zhang, Shanshan Zhang, Jia-Hao Wang, Meng-Rui Xu, Jing-Tian Ge, Zi-Qing Hu, Shang Lv, Lijuan Feng, Guofu Huang\",\"doi\":\"10.1039/d5qo00495k\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"α-Amidoketones are essential structural motifs in pharmaceuticals and synthetic chemistry. In this study, we describe a novel synthetic method that involves a cascade addition reaction, followed by a Lewis acid-catalyzed rearrangement of methyleneaziridines and carboxylic acids. Additionally, we developed a high-speed continuous flow synthesis method, allowing the reaction to proceed efficiently within 3.5 minutes. The incorporation of a greener silica gel-packed catalyzed column in this continuous flow system effectively facilitates the rearrangement step, providing a more environmentally friendly approach for synthesizing α-amidoketone compounds.\",\"PeriodicalId\":97,\"journal\":{\"name\":\"Organic Chemistry Frontiers\",\"volume\":\"71 1\",\"pages\":\"\"},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2025-04-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic Chemistry Frontiers\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d5qo00495k\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5qo00495k","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
A Cascade Markovnikov Addition / Lewis Acid-Catalyzed Rearrangement of Methyleneaziridines and Carboxylic Acids: Continuous-Flow Synthesis of α-Amidoketones
α-Amidoketones are essential structural motifs in pharmaceuticals and synthetic chemistry. In this study, we describe a novel synthetic method that involves a cascade addition reaction, followed by a Lewis acid-catalyzed rearrangement of methyleneaziridines and carboxylic acids. Additionally, we developed a high-speed continuous flow synthesis method, allowing the reaction to proceed efficiently within 3.5 minutes. The incorporation of a greener silica gel-packed catalyzed column in this continuous flow system effectively facilitates the rearrangement step, providing a more environmentally friendly approach for synthesizing α-amidoketone compounds.
期刊介绍:
Organic Chemistry Frontiers is an esteemed journal that publishes high-quality research across the field of organic chemistry. It places a significant emphasis on studies that contribute substantially to the field by introducing new or significantly improved protocols and methodologies. The journal covers a wide array of topics which include, but are not limited to, organic synthesis, the development of synthetic methodologies, catalysis, natural products, functional organic materials, supramolecular and macromolecular chemistry, as well as physical and computational organic chemistry.