Synthesis of 2-thioxoimidazolines via reaction of 1-unsubstituted 3-aminoquinoline-2,4-diones with isothiocyanates
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference20 articles.
1. Molecular Rearrangement of 9b-Hydroxy-1H-imidazo[4,5-c]quinoline-2,4-diones - A Convenient Pathway to Spiro-Linked Imidazolidine-Oxindole Derivatives
2. Total Synthesis of Bioactive Marine Macrolides
3. Marine natural products
4. Reaction of 1-substituted 3-aminoquinoline-2,4-diones with isothiocyanates. An easy pathway to generate novel 2-thioxo-1′H-spiro[imidazoline-5,3′-indole]-2,2′-diones
5. Syntheses of 3-Aminoquinoline- 2,4(1H,3H)-diones
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1. Molecular Rearrangement of Pyrazino[2,3-c]quinolin-5(6H)-ones during Their Reaction with Isocyanic Acid;International Journal of Molecular Sciences;2022-05-13
2. Reaction of 1-substituted 3-(2-hydroxyethylamino)quinoline-2,4(1H,3H)-diones with isothiocyanic acid;Chemistry of Heterocyclic Compounds;2020-05
3. New esters with thioxoimidazoquinazoline ring – Synthesis, spectral characterization and quantum mechanical modelling;Journal of Molecular Structure;2018-08
4. Chemistry and Applications of 4-Hydroxyquinolin-2-one and Quinoline-2,4-dionebased Compounds;Current Organic Chemistry;2017-10-09
5. Reaction of 3-chloroquinoline-2,4-diones with ethanolamine and rearrangement of the reaction products;Tetrahedron;2017-03
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