Facile synthesis of thiadiazolo [2,3-b] quinazoline derivatives via the Japp-Klingemann Reaction
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
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3. New routes to aroylthiadiazolines and arylazothiazoles from phenylglyoxalyl bromide arylhydrazones and phenacyl thiocyanate
4. Conversion of 2,2-dichloroacetoacetanilides into 4-(hydroxymethyl)-2(1H)-quinolones
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1. Efficient synthesis of novel thiadiazolo[2,3-b]quinazolin-6-ones catalyzed by diphenhydramine hydrochloride-CoCl2⋅6H2O deep eutectic solvent;Scientific Reports;2024-01-16
2. Tetrabutylammonium Hydrogen Sulfate mediated Three-Component Reaction for the Synthesis of Thiadiazolo [2,3-b] Quinazolin-6-(7H)-ones and Antioxidant Activity;Materials Today: Proceedings;2019
3. Water-Mediated One-Pot Three-Component Reaction to Bifunctionalized Thiadiazoloquinazolinone-coumarin Hybrids: A Green Approach;ChemistrySelect;2018-03-13
4. Synthetic profile of thiadiazoloquinazolines;Phosphorus, Sulfur, and Silicon and the Related Elements;2017-08-28
5. Difference in α-thiocyanation of malonates, β-oxo esters and β-diketones with sodium thiocyanate and cerium(IV) ammonium nitrate;Mendeleev Communications;2016-05
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