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Chemistry of Thieno[2,3-c]quinoline Derivatives Part (VII), Reactivities, and Biological Activities
Mini-Reviews in Organic Chemistry ( IF 2.3 ) Pub Date : 2023-06-05 , DOI: 10.2174/1570193x20666230301153215
Moustafa A. Gouda 1, 2 , Rayan M. Alansari 3 , Ameen A. Abu-Hashem 4, 5 , Abdel-Rahman B.A. El-Gazzar 5 , Ahmed A. M. Abdelgawad 4, 6 , Mohammed A. Salem 7, 8
Affiliation  

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.

中文翻译:

噻吩并[2,3-c]喹啉衍生物的化学部分(VII)、反应性和生物活性

在这篇综述中,从多个角度介绍了许多噻吩并[2,3-c]喹啉衍生物(TQs2, 3-c),包括使用尖端设备的各种制备和加工技术。本综述中的许多化学过程展示了如何由芳胺、酮、醛、羧酸和其他化学试剂制备 (TQs2, 3-c)。钯加速酰胺化、串联 CC 和 CN 键的形成、Vilsmeier 反应和 Pictet-Spengler 化学反应被用来阐明 (TQs2, 3-c) 的制备过程。
更新日期:2023-06-05
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