Phosphine triggered [3+2] allenoate–acrylate annulation: a mechanistic enlightenment
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference37 articles.
1. Phosphine-Catalyzed Cycloaddition of 2,3-Butadienoates or 2-Butynoates with Electron-Deficient Olefins. A Novel [3 + 2] Annulation Approach to Cyclopentenes
2. Synthetic methodology using tertiary phosphines as nucleophilic catalysts
3. Nucleophilic Phosphine Organocatalysis
4. Reactions of Electron-Deficient Alkynes and Allenes under Phosphine Catalysis
5. A Phosphine-Catalyzed [3+2] Cycloaddition Strategy Leading to the First Total Synthesis of (−)-Hinesol
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1. Highly regio- and stereoselective (3 + 2) annulation reaction of allenoates with 3-methyleneindolin-2-ones catalyzed by a planar chiral [2.2]paracyclophane-based bifunctional phosphine–phenol catalyst;Organic & Biomolecular Chemistry;2024
2. Phosphine‐Catalyzed [3+2] Cycloaddition of Aza‐Aurones and Allenoates: Enantioselective Synthesis of 2‐Spirocyclopentyl‐Indolin‐3‐Ones;European Journal of Organic Chemistry;2022-12-27
3. Synthetic and Computational Study of the Enantioselective [3+2]-Cycloaddition of Chromones with MBH Carbonates;Organic Letters;2022-08-04
4. Effects of Anchimeric Assistance in Phosphonium Enolates Chemistry;Russian Journal of General Chemistry;2022-07
5. Asymmetric Synthesis of Cyclopentene Compounds Containing All-Carbon Quaternary Stereocenters by (3 + 2) Cycloaddition and Its Application in the Formal Synthesis of (R)-(−)-Puraquinonic Acid;The Journal of Organic Chemistry;2022-06-14
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