V. B. Kharitonov, M. A. Arsenov, A. A. Danshina, D. A. Loginov
{"title":"苯甲酸和炔基二步法合成异喹诺酮类药物及其与异香豆素的比较发光研究","authors":"V. B. Kharitonov, M. A. Arsenov, A. A. Danshina, D. A. Loginov","doi":"10.32931/io2228a","DOIUrl":null,"url":null,"abstract":"An efficient two-step protocol for the synthesis of isoquinolones (isoquinolin-1(2H)-ones) has been developed based on the C–H annulation of benzoic acids with alkynes followed by the treatment of the isocoumarins formed with ammonium formate. This approach was applied for the synthesis of naturally occurring isoquinolone siaminine A. A comparative study of the optical properties revealed that isoquinolones display stronger luminescence emission than isocoumarins.","PeriodicalId":490007,"journal":{"name":"ИНЭОС OPEN","volume":"66 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Facile Two-Step Synthesis of Isoquinolones from Benzoic Acids and Alkynes and Their Comparative Photoluminescent Study vs Isocoumarins\",\"authors\":\"V. B. Kharitonov, M. A. Arsenov, A. A. Danshina, D. A. Loginov\",\"doi\":\"10.32931/io2228a\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"An efficient two-step protocol for the synthesis of isoquinolones (isoquinolin-1(2H)-ones) has been developed based on the C–H annulation of benzoic acids with alkynes followed by the treatment of the isocoumarins formed with ammonium formate. This approach was applied for the synthesis of naturally occurring isoquinolone siaminine A. A comparative study of the optical properties revealed that isoquinolones display stronger luminescence emission than isocoumarins.\",\"PeriodicalId\":490007,\"journal\":{\"name\":\"ИНЭОС OPEN\",\"volume\":\"66 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-10-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ИНЭОС OPEN\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.32931/io2228a\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ИНЭОС OPEN","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.32931/io2228a","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Facile Two-Step Synthesis of Isoquinolones from Benzoic Acids and Alkynes and Their Comparative Photoluminescent Study vs Isocoumarins
An efficient two-step protocol for the synthesis of isoquinolones (isoquinolin-1(2H)-ones) has been developed based on the C–H annulation of benzoic acids with alkynes followed by the treatment of the isocoumarins formed with ammonium formate. This approach was applied for the synthesis of naturally occurring isoquinolone siaminine A. A comparative study of the optical properties revealed that isoquinolones display stronger luminescence emission than isocoumarins.