Zhibo Ma, Zheng Xiang, T. Luo, K. Lu, Zhibin Xu, Jia-Hua Chen, Zhen Yang
{"title":"通过Ugi和pd催化的分子内芳化反应合成功能化喹啉。","authors":"Zhibo Ma, Zheng Xiang, T. Luo, K. Lu, Zhibin Xu, Jia-Hua Chen, Zhen Yang","doi":"10.1002/CHIN.200704139","DOIUrl":null,"url":null,"abstract":"Two types of quinoline scaffolds were constructed in a combinatorial format via the Ugi four-component reaction (U-4CR) and Pd-catalyzed intramolecular arylation reaction. The scope of this two-step synthetic sequence was examined from commercially available and synthetically accessible starting materials.","PeriodicalId":15439,"journal":{"name":"Journal of combinatorial chemistry","volume":"8 5 1","pages":"696-704"},"PeriodicalIF":0.0000,"publicationDate":"2006-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/CHIN.200704139","citationCount":"37","resultStr":"{\"title\":\"Synthesis of functionalized quinolines via Ugi and Pd-catalyzed intramolecular arylation reactions.\",\"authors\":\"Zhibo Ma, Zheng Xiang, T. Luo, K. Lu, Zhibin Xu, Jia-Hua Chen, Zhen Yang\",\"doi\":\"10.1002/CHIN.200704139\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Two types of quinoline scaffolds were constructed in a combinatorial format via the Ugi four-component reaction (U-4CR) and Pd-catalyzed intramolecular arylation reaction. The scope of this two-step synthetic sequence was examined from commercially available and synthetically accessible starting materials.\",\"PeriodicalId\":15439,\"journal\":{\"name\":\"Journal of combinatorial chemistry\",\"volume\":\"8 5 1\",\"pages\":\"696-704\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2006-07-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1002/CHIN.200704139\",\"citationCount\":\"37\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of combinatorial chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/CHIN.200704139\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of combinatorial chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/CHIN.200704139","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Synthesis of functionalized quinolines via Ugi and Pd-catalyzed intramolecular arylation reactions.
Two types of quinoline scaffolds were constructed in a combinatorial format via the Ugi four-component reaction (U-4CR) and Pd-catalyzed intramolecular arylation reaction. The scope of this two-step synthetic sequence was examined from commercially available and synthetically accessible starting materials.