Min Xiang, Gang-Yong Liu, Hui-Mei Liu, Wen-Yi Zhou, Guang-Wei Wang, Fei Fei, Yun-Qing Jia and Li-Wen Shen
{"title":"邻酰基芳基MBH碳酸盐与香豆素的[4+2]环化:四氢染料[4,3-b]喹啉-6- 1†的易得性","authors":"Min Xiang, Gang-Yong Liu, Hui-Mei Liu, Wen-Yi Zhou, Guang-Wei Wang, Fei Fei, Yun-Qing Jia and Li-Wen Shen","doi":"10.1039/D4NJ04654D","DOIUrl":null,"url":null,"abstract":"<p >A [4+2] annulation reaction of <em>o</em>-acylamino-aryl MBH carbonates with 3-substituted coumarins has been developed. This method exhibits excellent substrate tolerance and constructs a series of tetrahydrochromeno[4,3-<em>b</em>]quinolin-6-ones with yields up to 95%. The application value of this method has also been demonstrated through a 50-fold scale-up.</p>","PeriodicalId":95,"journal":{"name":"New Journal of Chemistry","volume":" 3","pages":" 683-686"},"PeriodicalIF":2.5000,"publicationDate":"2024-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The [4+2] annulation of o-acylamino-aryl MBH carbonates with coumarins: facile access to tetrahydrochromeno[4,3-b]quinolin-6-ones†\",\"authors\":\"Min Xiang, Gang-Yong Liu, Hui-Mei Liu, Wen-Yi Zhou, Guang-Wei Wang, Fei Fei, Yun-Qing Jia and Li-Wen Shen\",\"doi\":\"10.1039/D4NJ04654D\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >A [4+2] annulation reaction of <em>o</em>-acylamino-aryl MBH carbonates with 3-substituted coumarins has been developed. This method exhibits excellent substrate tolerance and constructs a series of tetrahydrochromeno[4,3-<em>b</em>]quinolin-6-ones with yields up to 95%. The application value of this method has also been demonstrated through a 50-fold scale-up.</p>\",\"PeriodicalId\":95,\"journal\":{\"name\":\"New Journal of Chemistry\",\"volume\":\" 3\",\"pages\":\" 683-686\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2024-12-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"New Journal of Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/nj/d4nj04654d\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/nj/d4nj04654d","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
The [4+2] annulation of o-acylamino-aryl MBH carbonates with coumarins: facile access to tetrahydrochromeno[4,3-b]quinolin-6-ones†
A [4+2] annulation reaction of o-acylamino-aryl MBH carbonates with 3-substituted coumarins has been developed. This method exhibits excellent substrate tolerance and constructs a series of tetrahydrochromeno[4,3-b]quinolin-6-ones with yields up to 95%. The application value of this method has also been demonstrated through a 50-fold scale-up.