Transition metal-free strategies for the stereoselective construction of spirocyclopropyl oxindoles
Author:
Funder
National Science Foundation
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference84 articles.
1. Recent Progress on Routes to Spirooxindole Systems Derived from Isatin
2. Organocatalytic Asymmetric Assembly Reactions: Synthesis of Spirooxindoles via Organocascade Strategies
3. Rapid Access to Spirocyclic Oxindole Alkaloids: Application of the Asymmetric Palladium-Catalyzed [3 + 2] Trimethylenemethane Cycloaddition
4. Catalytic Asymmetric [3+2] Annulation of Allylsilanes with Isatins: Synthesis of Spirooxindoles
5. An N-Heterocyclic Carbene/Lewis Acid Strategy for the Stereoselective Synthesis of Spirooxindole Lactones
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1. Metal-free β,γ-C(sp3)–H difunctionalization of propanols: DMP-initiated asymmetric spirocyclopropanation;Chemical Communications;2024
2. 3-Phenacylideneoxindoles in organic synthesis: Recent developments;Tetrahedron Letters;2023-10
3. Substrate-Controlled Diastereo- and Enantiodivergent Synthesis of Bis-Spirocyclopropyloxindoles from Available Isatin as a Single Starting Material;The Journal of Organic Chemistry;2023-04-21
4. Construction of C2‐Spirocyclopropyl‐Indolin‐3‐Ones through Base‐Promoted [2+1] Annulation Reaction of Indolin‐3‐ones with Bromosulfonium Salts;European Journal of Organic Chemistry;2023-03-22
5. Asymmetric Synthesis of Spiro-3,3′-cyclopropyl Oxindoles via Vinylogous Michael Initiated Ring Closure Reaction;The Journal of Organic Chemistry;2022-12-05
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