Catalytically Generated Vanadium Enolates Formed via Interruption of the Meyer–Schuster Rearrangement as Useful Reactive Intermediates
Author:
Affiliation:
1. Department of Chemistry, Stanford University, 333 Campus Drive, Stanford, California 94305, United States
Funder
Chugai Pharmaceuticals
Tamaki Foundation
Publisher
American Chemical Society (ACS)
Subject
General Medicine,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.accounts.0c00285
Reference82 articles.
1. Contemporaneous Dual Catalysis: Chemoselective Cross-Coupling of Catalytic Vanadium–Allenoate and π-Allylpalladium Intermediates
2. Vanadium-Catalyzed Synthesis of Geometrically Defined Acyclic Tri- and Tetrasubstituted Olefins from Propargyl Alcohols
3. Vanadium-Catalyzed Coupling of Allenols with Electrophilic Halide Sources for the Formation of α-Halo-α′,β′-unsaturated Ketones
4. Enamine-Based Organocatalysis with Proline and Diamines: The Development of Direct Catalytic Asymmetric Aldol, Mannich, Michael, and Diels−Alder Reactions
5. Asymmetric Enamine Catalysis
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