Electronic differentiation competes with transition state sensitivity in palladium-catalyzed allylic substitutions
Author:
Publisher
Beilstein Institut
Subject
Organic Chemistry
Link
https://www.beilstein-journals.org/bjoc/content/pdf/1860-5397-3-36.pdf
Reference55 articles.
1. Carbon-carbon bond formation via palladium complexes
2. New synthetic reactions. Allylic alkylation
3. Asymmetric Transition Metal-Catalyzed Allylic Alkylations
4. Asymmetric Transition-Metal-Catalyzed Allylic Alkylations: Applications in Total Synthesis
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2. Synthesis, Coordination Properties and Application of New N , N ‐Ligands Based on Bornyl and Binaphthylazepine Chiral Backbones in Palladium‐Catalyzed Allylic Substitution Reactions;European Journal of Inorganic Chemistry;2011-05-10
3. Palladium-Catalyzed Enantioselective Allylic Substitution;Transition Metal Catalyzed Enantioselective Allylic Substitution in Organic Synthesis;2011
4. Selectivity in Palladium-Catalyzed Allylic Substitution;Transition Metal Catalyzed Enantioselective Allylic Substitution in Organic Synthesis;2011
5. Synthesis and Characterization of New, Chiral P−N Ligands and Their Use in Asymmetric Allylic Alkylation;Organometallics;2010-11-16
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