Recyclization in the Series of Spiro[indole-3,5′-pyrimido[4,5-b]quinoline]-2,2′,4′-triones Prepared by a Three-Component Reaction of Isatins with (Thio)barbituric Acids and Electron-Rich Anilines
Author:
Affiliation:
1. Institut für Chemie, Universität Rostock
2. Department of Chemistry, Ural Federal University
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry,Catalysis
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0032-1318273.pdf
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1. Adventures in the Chemistry of Multicomponent and Domino Reactions;European Journal of Organic Chemistry;2024-06-12
2. Single Step Upgradation of Isatin to Bioactive Fused Heterocycles via Ring Expansion Reactions;European Journal of Organic Chemistry;2023-12-19
3. Solvent‐free Darzens condensation of 3‐ chlorooxindoles with aryl aldehydes for diastereoselective construction of spiro‐epoxyoxindoles by grinding;Journal of Heterocyclic Chemistry;2022-12-21
4. A novel spirocyclic scaffold accessed via tandem Claisen rearrangement/intramolecular oxa-Michael addition;Beilstein Journal of Organic Chemistry;2022-12-06
5. Expedient Synthesis and Antibacterial Activity of Tetrahydro-1′H-spiro[indoline-3,4′-quinoline]-3′-carbonitrile Derivatives Using Piperidine as Catalyst;Synlett;2021-01-22
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