Direct sulfanylation of 4-hydroxycoumarins with thiols in water
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference31 articles.
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2. General and Efficient Route for the Synthesis of 3,4-Disubstituted Coumarins via Pd-Catalyzed Site-Selective Cross-Coupling Reactions
3. RhCl(PPh3)3/DPPF: A Useful and Efficient Catalyst for Cross-Coupling Reactions of Activated Alkenyl Tosylates with Arylboronic Acids
4. Facile synthesis of chromeno[4,3-b]quinolin-6-ones from unexpected reactions of aryl isocyanides with 4-chloro-2-oxo-2H-chromene-3-carbaldehyde
5. Palladium-catalyzed Suzuki–Miyaura couplings of potassium aryl trifluoroborates with 4-tosyloxycoumarins or 4-tosyloxyquinolin-2(1H)-one
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1. Phosphorus ligand-free Suzuki–Miyaura reactions in the presence of ABTS at room temperature in water;Canadian Journal of Chemistry;2021-05
2. Efficient synthesis of 4-sulfanylcoumarins from 3-bromo-coumarins via a highly selective DABCO-mediated one-pot thia-Michael addition/elimination process;RSC Advances;2020
3. Recent advances in 4-hydroxycoumarin chemistry. Part 1: Synthesis and reactions;Arabian Journal of Chemistry;2019-01
4. An efficient route to 4-aryloxycoumarins via one-pot reactions of 4-hydroxycoumarins with hypervalent iodine reagents;Tetrahedron Letters;2017-10
5. Domino reactions of alkenyl p -benzoquinones: Access to aryl sulfide derivatives of coumarins;Tetrahedron;2017-05
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