可回收氧化铜催化芳烃卤化物与反式-4-羟基- l -脯氨酸合成N -芳基吡咯

R. Sridhar, M. Yedukondalu, N. Chandrasekhar, M. Rao
{"title":"可回收氧化铜催化芳烃卤化物与反式-4-羟基- l -脯氨酸合成N -芳基吡咯","authors":"R. Sridhar, M. Yedukondalu, N. Chandrasekhar, M. Rao","doi":"10.5923/J.MATERIALS.20110102.16","DOIUrl":null,"url":null,"abstract":"A facile and novel copper oxide nanoparticle catalyzed route has been developed for the synthesis of N-arylpyrroles, through tandem one-pot cross-coupling reaction of aryl halides and trans-4-hydroxy-L-proline, which is procured from natural source. This methodology is a first report of ligand free conditions and is a sustainable resource, via extrusion followed by redox amination. Catalyst used can be recovered and recycled up to five cycles with efficient activity.","PeriodicalId":7420,"journal":{"name":"American Journal of Materials Science","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2012-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Recyclable Copper Oxide Catalyzed Synthesis of N -Arylpyrroles from Arylhalides and Trans-4-Hydroxy-L-Proline\",\"authors\":\"R. Sridhar, M. Yedukondalu, N. Chandrasekhar, M. Rao\",\"doi\":\"10.5923/J.MATERIALS.20110102.16\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A facile and novel copper oxide nanoparticle catalyzed route has been developed for the synthesis of N-arylpyrroles, through tandem one-pot cross-coupling reaction of aryl halides and trans-4-hydroxy-L-proline, which is procured from natural source. This methodology is a first report of ligand free conditions and is a sustainable resource, via extrusion followed by redox amination. Catalyst used can be recovered and recycled up to five cycles with efficient activity.\",\"PeriodicalId\":7420,\"journal\":{\"name\":\"American Journal of Materials Science\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2012-08-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American Journal of Materials Science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5923/J.MATERIALS.20110102.16\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Materials Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5923/J.MATERIALS.20110102.16","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

利用天然来源的芳烃卤化物与反式-4-羟基- l -脯氨酸进行串联一锅交叉偶联反应,建立了一种简便、新颖的纳米氧化铜催化合成n -芳基吡咯的途径。这种方法是配体自由条件的第一份报告,是一种可持续的资源,通过挤压和氧化还原胺化。使用的催化剂可以回收和循环利用多达五次,具有高效的活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recyclable Copper Oxide Catalyzed Synthesis of N -Arylpyrroles from Arylhalides and Trans-4-Hydroxy-L-Proline
A facile and novel copper oxide nanoparticle catalyzed route has been developed for the synthesis of N-arylpyrroles, through tandem one-pot cross-coupling reaction of aryl halides and trans-4-hydroxy-L-proline, which is procured from natural source. This methodology is a first report of ligand free conditions and is a sustainable resource, via extrusion followed by redox amination. Catalyst used can be recovered and recycled up to five cycles with efficient activity.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信