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Chemistry of Thieno [2,3-h]-/[3,2-h] Quinoline and Thieno [2,3-f]-/[3,2-f] Quinoline Derivatives Part (x), Reactivities, and Biological Activities
Mini-Reviews in Organic Chemistry ( IF 2.3 ) Pub Date : 2023-06-23 , DOI: 10.2174/1570193x20666230525120540
Moustafa A. Gouda 1, 2 , Nahlah A. Al-Hadhrami 3 , Ameen A. Abu-Hashem 4, 5 , Ahmed A. M. Abdelgawad 4, 5 , Mohammed A. Salem 6, 7
Affiliation  

Several thieno [2,3-h] /[3,2-h] quinolines and thieno [2,3-f] /[3,2-f] quinolines (TQs) are discussed in this review from a few perspectives, including various preparation and processing methods employing cutting-edge machinery. The preparation of (TQs), from 4-(5)aminobenzothiophene, 2(3)chloromethylthiophene, 2(3)thienylboric acid, and other chemical reagents is illustrated via a number of chemical procedures in this review. The formation of (TQs) was clarified using the Michael addition, Photocyclization, Skraup reaction, Ullmann-Fetvadjian process, Suzuki-Miyaura and Sonogashira reaction, aza-Diels-Alder reaction, and Friedel-Crafts reaction.

中文翻译:

噻吩并 [2,3-h]-/[3,2-h] 喹啉和噻吩并 [2,3-f]-/[3,2-f] 喹啉衍生物的化学部分 (x)、反应性和生物活性

本综述从几个角度讨论了几种噻吩并[2,3-h]/[3,2-h]喹啉和噻吩并[2,3-f]/[3,2-f]喹啉(TQ),包括采用尖端机械的各种制备和加工方法。本综述通过许多化学程序说明了从 4-(5) 氨基苯并噻吩、2(3) 氯甲基噻吩、2(3) 噻吩基硼酸和其他化学试剂制备 (TQ) 的过程。使用Michael加成、光环化、Skraup反应、Ullmann-Fetvadjian法、Suzuki-Miyaura和Sonogashira反应、aza-Diels-Alder反应和Friedel-Crafts反应阐明了(TQs)的形成。
更新日期:2023-06-23
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