{"title":"通过一锅三组份反应合成新型 6H-呋喃并[3,2-e]吲哚衍生物","authors":"Dan-Dan Wan, Shuang-Ling Wu, Jia-Yan Liu, Dong-Sheng Chen","doi":"10.1002/jhet.4883","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>A one-pot, three-component reaction of ethyl 5-aminobenzofuran-2-carboxylate, arylglyoxals and cyclic 1,3-dicarbonyl compounds in the presence of acetic acid as an organocatalyst in ethanol medium under reflux conditions provided a series of new 6<i>H</i>-furo[3,2-<i>e</i>]indole derivatives in good yields.</p>\n </div>","PeriodicalId":194,"journal":{"name":"Journal of Heterocyclic Chemistry","volume":"61 10","pages":"1613-1621"},"PeriodicalIF":2.0000,"publicationDate":"2024-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis of Novel 6\\n H-Furo[3,2-e]Indole Derivatives via One-Pot Three Component Reactions\",\"authors\":\"Dan-Dan Wan, Shuang-Ling Wu, Jia-Yan Liu, Dong-Sheng Chen\",\"doi\":\"10.1002/jhet.4883\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <p>A one-pot, three-component reaction of ethyl 5-aminobenzofuran-2-carboxylate, arylglyoxals and cyclic 1,3-dicarbonyl compounds in the presence of acetic acid as an organocatalyst in ethanol medium under reflux conditions provided a series of new 6<i>H</i>-furo[3,2-<i>e</i>]indole derivatives in good yields.</p>\\n </div>\",\"PeriodicalId\":194,\"journal\":{\"name\":\"Journal of Heterocyclic Chemistry\",\"volume\":\"61 10\",\"pages\":\"1613-1621\"},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2024-08-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Heterocyclic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/jhet.4883\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Heterocyclic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jhet.4883","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Synthesis of Novel 6
H-Furo[3,2-e]Indole Derivatives via One-Pot Three Component Reactions
A one-pot, three-component reaction of ethyl 5-aminobenzofuran-2-carboxylate, arylglyoxals and cyclic 1,3-dicarbonyl compounds in the presence of acetic acid as an organocatalyst in ethanol medium under reflux conditions provided a series of new 6H-furo[3,2-e]indole derivatives in good yields.
期刊介绍：
The Journal of Heterocyclic Chemistry is interested in publishing research on all aspects of heterocyclic chemistry, especially development and application of efficient synthetic methodologies and strategies for the synthesis of various heterocyclic compounds. In addition, Journal of Heterocyclic Chemistry promotes research in other areas that contribute to heterocyclic synthesis/application, such as synthesis design, reaction techniques, flow chemistry and continuous processing, multiphase catalysis, green chemistry, catalyst immobilization and recycling.
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