One-pot approach for the stereoselective synthesis of spirocyclopropyl oxindoles from isatins and arsonium salts
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. Divergent Selectivity in MgI2-Mediated Ring Expansions of Methylenecyclopropyl Amides and Imides
2. A Homo [3+2] Dipolar Cycloaddition: The Reaction of Nitrones with Cyclopropanes
3. Ring-Expanding Reaction of Cyclopropyl Amides with Triphenylphosphine and Carbon Tetrahalide
4. Dimerization of Cyclopropyl Ketones and Crossed Reactions of Cyclopropyl Ketones with Enones as an Entry to Five-Membered Rings
5. Application of Reactive Enols in Synthesis: A Versatile, Efficient, and Stereoselective Construction of the Welwitindolinone Carbon Skeleton
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1. One-pot synthesis of biologically active oxazole, isoxazole, and pyranopyrazoles—an overview;Green Approaches in Medicinal Chemistry for Sustainable Drug Design;2024
2. Diastereoselective Sonochemical Synthesis of Spirocyclopropaneoxindoles and Evaluation of Their Antioxidant and Cytotoxic Activities;Chemistry & Biodiversity;2019-06-03
3. Solvent-Controlled, Tunable Domino Reaction of 3-Ylideneoxindoles with in Situ-Generated α-Aryldiazomethanes: A Facile Access to 3-Spirocyclopropyl-2-oxindole and Pyrazoloquinazolinone Scaffolds;ACS Omega;2018-10-01
4. Part I: Diastereoselective Reactions Involving β-Mono- and β,β′-Disubstituted Alkylidene Oxindoles: Pondering Alkene Geometry;Asian Journal of Organic Chemistry;2017-12-20
5. Lanthanide amide-catalyzed one-pot functionalization of isatins: synthesis of spiro[cyclopropan-1,3′-oxindoles] and 2-oxoindolin-3-yl phosphates;Organic & Biomolecular Chemistry;2017
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