{"title":"Lys-CQD催化合成硫脲,酰胺和甲酰胺化合物使用可再生和竞争性的原料。","authors":"Morteza Hasani , Hamid R. Kalhor , Masumeh Salehi , Fatemeh Rahgozar","doi":"10.1039/d5ob00772k","DOIUrl":null,"url":null,"abstract":"<div><div>The use of renewable and cheap precursors in chemical synthesis is highly beneficial, yet challenging due to their inert chemistry and the need for complex catalysts to enhance their reactivity. Herein, we demonstrate that a lysine-modified carbon quantum dot (Lys-CQD) catalyst is a promising catalyst for activating various carbonyl sources. Initially, in a one-pot 3-step reaction, Lys-CQD promoted the reaction of anilines with CS<sub>2</sub> toward the synthesis of thioureas. The reaction was performed in a choline chloride/urea deep eutectic solvent (ChCl/U DES), which also served as a urea-bearing precursor. Moreover, in the reaction of anilines with DMF, Lys-CQD proved to be a potent catalyst for synthesizing formamide products. Notably, DMF functioned as both the solvent and the carbonylation precursor. Lastly, the Lys-CQD-catalyzed reaction of various amines with vinyl acetate was exploited, furnishing different amides with high yields, including amide-containing drugs such as acedoben. The results highlight the strong potential of Lys-CQD as a clean catalyst for organic synthesis, particularly in activating unreactive carbonyl precursors.</div></div>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":"23 31","pages":"Pages 7320-7330"},"PeriodicalIF":2.7000,"publicationDate":"2025-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Lys-CQD catalyzed synthesis of thiourea, amide, and formamide compounds using renewable and competitive feedstocks†\",\"authors\":\"Morteza Hasani , Hamid R. Kalhor , Masumeh Salehi , Fatemeh Rahgozar\",\"doi\":\"10.1039/d5ob00772k\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The use of renewable and cheap precursors in chemical synthesis is highly beneficial, yet challenging due to their inert chemistry and the need for complex catalysts to enhance their reactivity. Herein, we demonstrate that a lysine-modified carbon quantum dot (Lys-CQD) catalyst is a promising catalyst for activating various carbonyl sources. Initially, in a one-pot 3-step reaction, Lys-CQD promoted the reaction of anilines with CS<sub>2</sub> toward the synthesis of thioureas. The reaction was performed in a choline chloride/urea deep eutectic solvent (ChCl/U DES), which also served as a urea-bearing precursor. Moreover, in the reaction of anilines with DMF, Lys-CQD proved to be a potent catalyst for synthesizing formamide products. Notably, DMF functioned as both the solvent and the carbonylation precursor. Lastly, the Lys-CQD-catalyzed reaction of various amines with vinyl acetate was exploited, furnishing different amides with high yields, including amide-containing drugs such as acedoben. The results highlight the strong potential of Lys-CQD as a clean catalyst for organic synthesis, particularly in activating unreactive carbonyl precursors.</div></div>\",\"PeriodicalId\":96,\"journal\":{\"name\":\"Organic & Biomolecular Chemistry\",\"volume\":\"23 31\",\"pages\":\"Pages 7320-7330\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-07-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic & Biomolecular Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1477052025005841\",\"RegionNum\":3,\"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 & Biomolecular Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1477052025005841","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Lys-CQD catalyzed synthesis of thiourea, amide, and formamide compounds using renewable and competitive feedstocks†
The use of renewable and cheap precursors in chemical synthesis is highly beneficial, yet challenging due to their inert chemistry and the need for complex catalysts to enhance their reactivity. Herein, we demonstrate that a lysine-modified carbon quantum dot (Lys-CQD) catalyst is a promising catalyst for activating various carbonyl sources. Initially, in a one-pot 3-step reaction, Lys-CQD promoted the reaction of anilines with CS2 toward the synthesis of thioureas. The reaction was performed in a choline chloride/urea deep eutectic solvent (ChCl/U DES), which also served as a urea-bearing precursor. Moreover, in the reaction of anilines with DMF, Lys-CQD proved to be a potent catalyst for synthesizing formamide products. Notably, DMF functioned as both the solvent and the carbonylation precursor. Lastly, the Lys-CQD-catalyzed reaction of various amines with vinyl acetate was exploited, furnishing different amides with high yields, including amide-containing drugs such as acedoben. The results highlight the strong potential of Lys-CQD as a clean catalyst for organic synthesis, particularly in activating unreactive carbonyl precursors.
期刊介绍:
Organic & Biomolecular Chemistry is an international journal using integrated research in chemistry-organic chemistry. Founded in 2003 by the Royal Society of Chemistry, the journal is published in Semimonthly issues and has been indexed by SCIE, a leading international database. The journal focuses on the key research and cutting-edge progress in the field of chemistry-organic chemistry, publishes and reports the research results in this field in a timely manner, and is committed to becoming a window and platform for rapid academic exchanges among peers in this field. The journal's impact factor in 2023 is 2.9, and its CiteScore is 5.5.