{"title":"可见光下吡啶盐光活化2 -炔芳基腈基碱辅助正交合成4 -芳基异喹啉二酮和氮杂醌","authors":"Shruti Rajput , Nidhi Jain","doi":"10.1002/adsc.70062","DOIUrl":null,"url":null,"abstract":"<div><div>A metal‐free, photooxidative activation of 2‐alkynylarylnitriles in presence of pyrylium salt as a photocatalyst is reported. The 1,2‐diketone intermediate generated in visible light demonstrates base‐assisted orthogonality toward cyclization, furnishing 4‐aryl‐4‐hydroxyisoquinoline‐1,3‐(2<em>H</em>,4<em>H</em>)‐dione and 3‐aryl‐3‐hydroxy‐2,3‐dihydroazanaphthoquinone derivatives. The reaction has a wide substrate scope, good functional group tolerance, uses an organic photocatalyst, and takes place at room temperature. Preliminary biological screening of synthesized molecules reveals their potential as anticancer agents.</div></div>","PeriodicalId":118,"journal":{"name":"Advanced Synthesis & Catalysis","volume":"367 18","pages":"Article e70062"},"PeriodicalIF":4.0000,"publicationDate":"2025-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Base‐Assisted Orthogonal Synthesis of 4‐Arylisoquinolinediones and Azanaphthoquinones from 2‐Alkynylarylnitriles via Photoactivation by Pyrylium Salt in Visible Light\",\"authors\":\"Shruti Rajput , Nidhi Jain\",\"doi\":\"10.1002/adsc.70062\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A metal‐free, photooxidative activation of 2‐alkynylarylnitriles in presence of pyrylium salt as a photocatalyst is reported. The 1,2‐diketone intermediate generated in visible light demonstrates base‐assisted orthogonality toward cyclization, furnishing 4‐aryl‐4‐hydroxyisoquinoline‐1,3‐(2<em>H</em>,4<em>H</em>)‐dione and 3‐aryl‐3‐hydroxy‐2,3‐dihydroazanaphthoquinone derivatives. The reaction has a wide substrate scope, good functional group tolerance, uses an organic photocatalyst, and takes place at room temperature. Preliminary biological screening of synthesized molecules reveals their potential as anticancer agents.</div></div>\",\"PeriodicalId\":118,\"journal\":{\"name\":\"Advanced Synthesis & Catalysis\",\"volume\":\"367 18\",\"pages\":\"Article e70062\"},\"PeriodicalIF\":4.0000,\"publicationDate\":\"2025-09-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Synthesis & Catalysis\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1615415025002912\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Synthesis & Catalysis","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1615415025002912","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
Base‐Assisted Orthogonal Synthesis of 4‐Arylisoquinolinediones and Azanaphthoquinones from 2‐Alkynylarylnitriles via Photoactivation by Pyrylium Salt in Visible Light
A metal‐free, photooxidative activation of 2‐alkynylarylnitriles in presence of pyrylium salt as a photocatalyst is reported. The 1,2‐diketone intermediate generated in visible light demonstrates base‐assisted orthogonality toward cyclization, furnishing 4‐aryl‐4‐hydroxyisoquinoline‐1,3‐(2H,4H)‐dione and 3‐aryl‐3‐hydroxy‐2,3‐dihydroazanaphthoquinone derivatives. The reaction has a wide substrate scope, good functional group tolerance, uses an organic photocatalyst, and takes place at room temperature. Preliminary biological screening of synthesized molecules reveals their potential as anticancer agents.
期刊介绍:
Advanced Synthesis & Catalysis (ASC) is the leading primary journal in organic, organometallic, and applied chemistry.
The high impact of ASC can be attributed to the unique focus of the journal, which publishes exciting new results from academic and industrial labs on efficient, practical, and environmentally friendly organic synthesis. While homogeneous, heterogeneous, organic, and enzyme catalysis are key technologies to achieve green synthesis, significant contributions to the same goal by synthesis design, reaction techniques, flow chemistry, and continuous processing, multiphase catalysis, green solvents, catalyst immobilization, and recycling, separation science, and process development are also featured in ASC. The Aims and Scope can be found in the Notice to Authors or on the first page of the table of contents in every issue.