{"title":"通过串联 1,3-二极环加成和氧化脱氢微波辅助合成吡咯烷基螺氧吲哚","authors":"Hong-bo Tan , Yu-heng Xiang , Jing-wen Huang , Si-ying Ren , Chang-qiu Lin , Zhi-gang Xu , Dian-yong Tang , Zhong-zhu Chen","doi":"10.1016/j.tet.2024.134379","DOIUrl":null,"url":null,"abstract":"<div><div>An oxidant-free, microwave-promoted tandem 1,3-dipolar cycloaddition and dehydrogenation oxidation is achieved under environmentally friendly conditions, delivering novel fused pyrrolidinyl-spirooxindoles in good to excellent yields. This work provides powerful means to expand the structural diversity of pyrrolidinyl-spirooxindole as a promising scaffold for novel drug discovery.</div></div>","PeriodicalId":437,"journal":{"name":"Tetrahedron","volume":"169 ","pages":"Article 134379"},"PeriodicalIF":2.1000,"publicationDate":"2024-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Microwave-assisted synthesis of pyrrolidinyl-spirooxindoles via tandem 1,3-dipolar cycloaddition and oxidative dehydrogenation\",\"authors\":\"Hong-bo Tan , Yu-heng Xiang , Jing-wen Huang , Si-ying Ren , Chang-qiu Lin , Zhi-gang Xu , Dian-yong Tang , Zhong-zhu Chen\",\"doi\":\"10.1016/j.tet.2024.134379\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>An oxidant-free, microwave-promoted tandem 1,3-dipolar cycloaddition and dehydrogenation oxidation is achieved under environmentally friendly conditions, delivering novel fused pyrrolidinyl-spirooxindoles in good to excellent yields. This work provides powerful means to expand the structural diversity of pyrrolidinyl-spirooxindole as a promising scaffold for novel drug discovery.</div></div>\",\"PeriodicalId\":437,\"journal\":{\"name\":\"Tetrahedron\",\"volume\":\"169 \",\"pages\":\"Article 134379\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2024-11-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Tetrahedron\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S004040202400560X\",\"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":"Tetrahedron","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S004040202400560X","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Microwave-assisted synthesis of pyrrolidinyl-spirooxindoles via tandem 1,3-dipolar cycloaddition and oxidative dehydrogenation
An oxidant-free, microwave-promoted tandem 1,3-dipolar cycloaddition and dehydrogenation oxidation is achieved under environmentally friendly conditions, delivering novel fused pyrrolidinyl-spirooxindoles in good to excellent yields. This work provides powerful means to expand the structural diversity of pyrrolidinyl-spirooxindole as a promising scaffold for novel drug discovery.
期刊介绍:
Tetrahedron publishes full accounts of research having outstanding significance in the broad field of organic chemistry and its related disciplines, such as organic materials and bio-organic chemistry.
Regular papers in Tetrahedron are expected to represent detailed accounts of an original study having substantially greater scope and details than that found in a communication, as published in Tetrahedron Letters.
Tetrahedron also publishes thematic collections of papers as special issues and ''Reports'', commissioned in-depth reviews providing a comprehensive overview of a research area.