Synthesis of 3,5-bis(acyl)-1,2,4-thiadiazoles via iodine mediated oxidative dimerization of α-oxothioamides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference43 articles.
1. Selective inhibition of bacterial dihydroorotate dehydrogenases by thiadiazolidinediones
2. Novel 1,2,4-oxadiazoles and 1,2,4-thiadiazoles as dual 5-lipoxygenase and cyclooxygenase inhibitors
3. Thiazole and Thiadiazole Analogues as a Novel Class of Adenosine Receptor Antagonists
4. Discovery of Novel 1,2,4-Thiadiazole Derivatives as Potent, Orally Active Agonists of Sphingosine 1-Phosphate Receptor Subtype 1 (S1P1)
5. Synthesis and Angiotensin II Receptor Antagonistic Activities of Benzimidazole Derivatives Bearing Acidic Heterocycles as Novel Tetrazole Bioisosteres
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. A chromatography-free one-pot, two-step synthesis of 1,2,4-thiadiazoles from primary amides via thiolation and oxidative dimerization under solvent-free conditions: a greener approach;RSC Advances;2024
2. Electrochemical Synthesis of 3,5-Bis(acyl)-1,2,4-thiadiazoles through <i>n</i>-Bu<sub>4</sub>NI-mediated Oxidative Dimerization of α-Oxothioamides;Electrochemistry;2023-12-28
3. A panoramic view on synthetic applications of α-oxothioamides: a highly regioselective synthesis of 2-acyl-4-(het)arylthiazoles and thioethers;RSC Advances;2023
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