Copper-catalysed approach to spirocyclic oxindoles via a direct C–H, Ar-H functionalisation
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference48 articles.
1. 3‐Alkenyl‐oxindoles: Natural Products, Pharmaceuticals, and Recent Synthetic Advances in Tandem/Telescoped Approaches
2. Catalytic Asymmetric Synthesis of Oxindoles Bearing a Tetrasubstituted Stereocenter at the C-3 Position
3. Oxindoles and copper complexes with oxindole-derivatives as potential pharmacological agents
4. Asymmetric Syntheses of Oxindole and Indole Spirocyclic Alkaloid Natural Products
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1. Oxindole synthesis via C H activation methods;Advances in Heterocyclic Chemistry;2023
2. Asymmetric Synthesis of Spiro[Azetidine‐3,3′‐Indoline]‐2,2′‐Diones via Copper(I)‐Catalyzed Kinugasa/C−C Coupling Cascade Reaction;Angewandte Chemie International Edition;2022-09-19
3. Asymmetric Synthesis of Spiro[Azetidine‐3,3′‐Indoline]‐2,2′‐Diones via Copper(I)‐Catalyzed Kinugasa/C−C Coupling Cascade Reaction;Angewandte Chemie;2022-09-19
4. Iridium-catalyzed Enantioselective Intramolecular Cross-dehydrogenative Coupling of Alkyl Aryl Ethers Giving Enantioenriched 2,3-Dihydrobenzofurans;Chemistry Letters;2022-06-05
5. A new synthetic approach to oxindoles (1,3-dihydro-2H-indol-2-ones) by reductive dephosphorylation with hydroiodic acid of 3-(diethylphosphoryloxy)- oxindoles, derived from isatins (1H-Indole-2,3-diones);Arkivoc;2022-04-21
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