A computational study of the activation of allenoates by Lewis bases and the reactivity of intermediate adducts
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2014/OB/C4OB01177E
Reference69 articles.
1. Modern Allene Chemistry, ed. N. Krause and A. S. K. Hashmi, Wiley-VCH, Weinheim, 2004
2. Some Typical Advances in the Synthetic Applications of Allenes
3. Allenes in Catalytic Asymmetric Synthesis and Natural Product Syntheses
4. Allenes as Three‐Carbon Units in Catalytic Cycloadditions: New Opportunities with Transition‐Metal Catalysts
5. Reactions of Electron-Deficient Alkynes and Allenes under Phosphine Catalysis
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1. Isochalcogenourea-catalyzed asymmetric (4 + 2)-heterocycloadditions of allenoates;Chemistry Letters;2024-08-23
2. Enantioselective Syntheses of 3,4‐Dihydropyrans Employing Isochalcogenourea‐Catalyzed Formal (4+2)‐Cycloadditions of Allenoates;Advanced Synthesis & Catalysis;2024-03-22
3. 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
4. Chiral Isochalcogenourea‐Catalysed Enantioselective (4+2) Cycloadditions of Allenoates;Angewandte Chemie International Edition;2023-12-11
5. Chiral Isochalcogenourea‐Catalysed Enantioselective (4+2) Cycloadditions of Allenoates;Angewandte Chemie;2023-12-11
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