Chemistry of Thieno[2,3-c]quinoline Derivatives Part (VII), Reactivities, and Biological Activities-Reference-Cited by-同舟云学术

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

Published:2024-08 Issue:5 Volume:21 Page:527-541
ISSN:1570-193X
Container-title:Mini-Reviews in Organic Chemistry
language:en
Short-container-title:MROC

Author:

Gouda Moustafa A.¹²,Alansari Rayan M.³,Abu-Hashem Ameen A.⁴⁵,El-Gazzar Abdel-Rahman B.A.⁴,Abdelgawad Ahmed A.M.⁵⁶,Salem Mohammed A.⁷

Affiliation:

1. Department of Chemistry, Faculty of Science and Arts, Taibah University, Ulla, Medina, Saudi Arabia

2. Department of Chemistry, Faculty of Science, Mansoura University, Mansoura, 35516, Egypt

3. Department of Biology, Faculty of Science and Arts, Taibah University, Ulla, Medina, Saudi Arabia

4. Department of Photochemistry, (Heterocyclic Unit), National Research Centre, Dokki, Giza, 12622, Egypt

5. Chemistry Departments, Faculty of Science, Jazan University, Jazan, 45142, Saudi Arabia

6. Department of Medicinal and Aromatic Plants, Desert Research Center, Cairo, Egypt

7. Department of Chemistry, Faculty of Science and Arts, King Khalid University, Mohail Assir, KSA

Abstract

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.

Funder

Deanship of Scientific Research at King Khalid University

Publisher

Bentham Science Publishers Ltd.

Subject

Organic Chemistry

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