“Iron catalyzed alkynylation of thiohydantoins with terminal alkyne via cross-dehydrogenative coupling (CDC)”
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference34 articles.
1. 2H-chromene derivatives bearing thiazolidine-2,4-dione, rhodanine or hydantoin moieties as potential anticancer agents
2. Design, synthesis, anticonvulsant, and antiarrhythmic properties of novel N-Mannich base and amide derivatives of β-tetralinohydantoin
3. 1-Benzyl-3-aryl-2-thiohydantoin Derivatives as New Anti-Trypanosoma brucei Agents: SAR and in Vivo Efficacy
4. Discovery of highly selective 7-chloroquinoline-thiohydantoins with potent antimalarial activity
5. Synthesis and antibacterial activity of Schiff bases of 5-substituted isatins
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1. Iron-Catalyzed Oxidative C(sp3)–C(sp3) Radical Coupling Reaction between Thiohydantoins and O-Acetyloximes for the Synthesis of 1,3-Dibenzyl-3,4-dihydropyrrolo[2,3-d]imidazole-2(1H)-thione Derivatives;Synlett;2024-04-09
2. Cu‐catalyzed dehydrogenative CO arylation for the synthesis of 6‐methyl benzofuro[3,2‐c] quinoline derivatives;Journal of Heterocyclic Chemistry;2024-01-07
3. Synthesis of 2-thioxoimidazolidin-4-one derivatives (microreview);Chemistry of Heterocyclic Compounds;2023-09
4. Facile synthesis of chromeno fused imidazolidinone derivatives via copper‐catalyzed tandem O‐arylation/oxidative acylation protocol;ChemistrySelect;2023-08-16
5. Synthesis of 5-methylidene-2-thio- and 2-selenohydantoins from isothiocyanates or isoselenocyanates and l-serine;Mendeleev Communications;2022-11
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