Chemistry of Thieno[2,3-c]quinoline derivatives part (VII), Reactivities, and Biological Activities

IF 1.9 4区 化学 Q2 CHEMISTRY, ORGANIC
M. Gouda, Rayan M. Alansari, A. Abu‐Hashem, Abdel-Rhman B. A. El-Gazzar, Ahmed A. M. Abdelgawad, M. A. Salem
{"title":"Chemistry of Thieno[2,3-c]quinoline derivatives part (VII), Reactivities, and Biological Activities","authors":"M. Gouda, Rayan M. Alansari, A. Abu‐Hashem, Abdel-Rhman B. A. El-Gazzar, Ahmed A. M. Abdelgawad, M. A. Salem","doi":"10.2174/1570193x20666230301153215","DOIUrl":null,"url":null,"abstract":"\n\nIn this review, numerous thieno[2,3-c]quinoline derivatives (TQs2, 3-c) are presented from a variety of angles, including various preparation and processing techniques, using cutting-edge equipment. Numerous chemical processes in this review demonstrate how (TQs2, 3-c) were made from arylamines, ketones, aldehydes, carboxylic acids, and other chemical reagents. The amidation, tandem C-C and C-N bond creation accelerated by palladium, Vilsmeier reaction, and Pictet-Spengler chemical reactions were used to shed light on how (TQs2, 3-c) was made.\n","PeriodicalId":18632,"journal":{"name":"Mini-reviews in Organic Chemistry","volume":" ","pages":""},"PeriodicalIF":1.9000,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mini-reviews in Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.2174/1570193x20666230301153215","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

Abstract

In this review, numerous thieno[2,3-c]quinoline derivatives (TQs2, 3-c) are presented from a variety of angles, including various preparation and processing techniques, using cutting-edge equipment. Numerous chemical processes in this review demonstrate how (TQs2, 3-c) were made from arylamines, ketones, aldehydes, carboxylic acids, and other chemical reagents. The amidation, tandem C-C and C-N bond creation accelerated by palladium, Vilsmeier reaction, and Pictet-Spengler chemical reactions were used to shed light on how (TQs2, 3-c) was made.
噻吩并[2,3-c]喹啉衍生物的化学第(VII)部分,反应性和生物活性
本文从多个角度介绍了噻吩[2,3-c]喹啉衍生物(TQs2, 3-c),包括各种制备和加工技术,并采用了先进的设备。在这篇综述中,许多化学过程展示了如何从芳胺、酮类、醛类、羧酸和其他化学试剂中制备(TQs2, 3-c)。通过钯加速的酰胺化、串联C-C和C-N键生成、Vilsmeier反应和Pictet-Spengler化学反应,阐明了(TQs2, 3-c)的生成过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Mini-reviews in Organic Chemistry
Mini-reviews in Organic Chemistry 化学-有机化学
CiteScore
4.50
自引率
4.30%
发文量
116
审稿时长
>12 weeks
期刊介绍: Mini-Reviews in Organic Chemistry is a peer reviewed journal which publishes original reviews on all areas of organic chemistry including organic synthesis, bioorganic and medicinal chemistry, natural product chemistry, molecular recognition, and physical organic chemistry. The emphasis will be on publishing quality papers very rapidly, without any charges. The journal encourages submission of reviews on emerging fields of organic chemistry including: Bioorganic Chemistry Carbohydrate Chemistry Chemical Biology Chemical Process Research Computational Organic Chemistry Development of Synthetic Methodologies Functional Organic Materials Heterocyclic Chemistry Macromolecular Chemistry Natural Products Isolation And Synthesis New Synthetic Methodology Organic Reactions Organocatalysis Organometallic Chemistry Theoretical Organic Chemistry Polymer Chemistry Stereochemistry Structural Investigations Supramolecular Chemistry
×
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