Enantioselective Formation of Quaternary Centers by Allylic Alkylation with First-Row Transition-Metal Catalysts
Author:
Affiliation:
1. The Warren and Katharine Schlinger Laboratory for Chemistry and Chemical Engineering, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, United States
Funder
Alexander von Humboldt-Stiftung
National Institute of General Medical Sciences
California Institute of Technology
Publisher
American Chemical Society (ACS)
Subject
General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.chemrev.0c01115
Reference95 articles.
1. All-carbon quaternary centers in natural products and medicinal chemistry: recent advances
2. Catalytic enantioselective synthesis of quaternary carbon stereocentres
3. The total synthesis of (-)-cyanthiwigin F by means of double catalytic enantioselective alkylation
4. Diastereodivergent Reverse Prenylation of Indole and Tryptophan Derivatives: Total Synthesis of Amauromine, Novoamauromine, and epi -Amauromine
5. Enantioselective Rhodium-Catalyzed Allylic Substitution with a Nitrile Anion: Construction of Acyclic Quaternary Carbon Stereogenic Centers
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