Strategy for Employing Unstabilized Nucleophiles in Palladium-Catalyzed Asymmetric Allylic Alkylations
Author:
Affiliation:
1. Department of Chemistry, Stanford University, Stanford, California 94305-5080
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja806781u
Reference15 articles.
1. Asymmetric Transition-Metal-Catalyzed Allylic Alkylations: Applications in Total Synthesis
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3. Fonctionnalisation en position allylique d'olefine methylenique par action d'un reactif nucleophile sur leur complexe palladie.
4. Regioselectivity in organo-transition-metal chemistry. A new indicator substrate for classification of nucleophiles
5. Studies on the Mechanism of Allylic Coupling Reactions: A Hammett Analysis of the Coupling of Aryl Silicate Derivatives
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