Qiong-Hui Peng , Ning-Bo Li , Jia-Cheng Hou , Cai-Jun He , Ya-Xin Yang , Chun-Lin Zhuang , Li-Juan Ou , Mei Yuan , Wei-Min He
{"title":"Nd@g-C3N4 3-氟烷基化喹啉-2(1H)- 1的双功能光合作用和抗肿瘤活性","authors":"Qiong-Hui Peng , Ning-Bo Li , Jia-Cheng Hou , Cai-Jun He , Ya-Xin Yang , Chun-Lin Zhuang , Li-Juan Ou , Mei Yuan , Wei-Min He","doi":"10.1016/j.cclet.2025.111402","DOIUrl":null,"url":null,"abstract":"<div><div>Herein, the Nd@g-C<sub>3</sub>N<sub>4</sub> dual-functional photocatalysis enabled fluoroalkylative heteroarylation of alkenes with R<sub>f</sub>SO<sub>2</sub>Cl under visible-light and ultrasound conditions was firstly reported. The photogenerated electron-driven reductive production of fluoroalkyl radical paired with photogenerated hole-driven oxidative production of chloride radical resulted in the full utilization of photogenerated carrier for bond formation. A wide range of <em>N</em>-heteroarenes, alkenes and R<sub>f</sub>SO<sub>2</sub>Cl, were well compatible for this reaction to access valuable fluoroalkylated <em>N</em>-heteroarenes with diverse structural features. The antitumor potential of synthesized fluoroalkylated <em>N</em>-heterocycles against Glioma 261 cells was evaluated by CCK8 assay. Notably, compound <strong>4aka</strong> demonstrated remarkable efficacy, exhibiting approximately sevenfold greater potency than temozolomide, a widely used chemotherapeutic agent.</div></div>","PeriodicalId":10088,"journal":{"name":"Chinese Chemical Letters","volume":"36 12","pages":"Article 111402"},"PeriodicalIF":8.9000,"publicationDate":"2025-05-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Nd@g-C3N4 dual-functional photosynthesis and antitumor activities of 3-fluoroalkylated quinoxalin-2(1H)-ones\",\"authors\":\"Qiong-Hui Peng , Ning-Bo Li , Jia-Cheng Hou , Cai-Jun He , Ya-Xin Yang , Chun-Lin Zhuang , Li-Juan Ou , Mei Yuan , Wei-Min He\",\"doi\":\"10.1016/j.cclet.2025.111402\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Herein, the Nd@g-C<sub>3</sub>N<sub>4</sub> dual-functional photocatalysis enabled fluoroalkylative heteroarylation of alkenes with R<sub>f</sub>SO<sub>2</sub>Cl under visible-light and ultrasound conditions was firstly reported. The photogenerated electron-driven reductive production of fluoroalkyl radical paired with photogenerated hole-driven oxidative production of chloride radical resulted in the full utilization of photogenerated carrier for bond formation. A wide range of <em>N</em>-heteroarenes, alkenes and R<sub>f</sub>SO<sub>2</sub>Cl, were well compatible for this reaction to access valuable fluoroalkylated <em>N</em>-heteroarenes with diverse structural features. The antitumor potential of synthesized fluoroalkylated <em>N</em>-heterocycles against Glioma 261 cells was evaluated by CCK8 assay. Notably, compound <strong>4aka</strong> demonstrated remarkable efficacy, exhibiting approximately sevenfold greater potency than temozolomide, a widely used chemotherapeutic agent.</div></div>\",\"PeriodicalId\":10088,\"journal\":{\"name\":\"Chinese Chemical Letters\",\"volume\":\"36 12\",\"pages\":\"Article 111402\"},\"PeriodicalIF\":8.9000,\"publicationDate\":\"2025-05-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chinese Chemical Letters\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1001841725005868\",\"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":"Chinese Chemical Letters","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1001841725005868","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Nd@g-C3N4 dual-functional photosynthesis and antitumor activities of 3-fluoroalkylated quinoxalin-2(1H)-ones
Herein, the Nd@g-C3N4 dual-functional photocatalysis enabled fluoroalkylative heteroarylation of alkenes with RfSO2Cl under visible-light and ultrasound conditions was firstly reported. The photogenerated electron-driven reductive production of fluoroalkyl radical paired with photogenerated hole-driven oxidative production of chloride radical resulted in the full utilization of photogenerated carrier for bond formation. A wide range of N-heteroarenes, alkenes and RfSO2Cl, were well compatible for this reaction to access valuable fluoroalkylated N-heteroarenes with diverse structural features. The antitumor potential of synthesized fluoroalkylated N-heterocycles against Glioma 261 cells was evaluated by CCK8 assay. Notably, compound 4aka demonstrated remarkable efficacy, exhibiting approximately sevenfold greater potency than temozolomide, a widely used chemotherapeutic agent.
期刊介绍:
Chinese Chemical Letters (CCL) (ISSN 1001-8417) was founded in July 1990. The journal publishes preliminary accounts in the whole field of chemistry, including inorganic chemistry, organic chemistry, analytical chemistry, physical chemistry, polymer chemistry, applied chemistry, etc.Chinese Chemical Letters does not accept articles previously published or scheduled to be published. To verify originality, your article may be checked by the originality detection service CrossCheck.