“Goldilocks Effect” of Water in Lewis-Brønsted Acid and Base Catalysis
Author:
Affiliation:
1. Department of Chemistry, Imperial College London, South Kensington, London SW7 2AZ, United Kingdom
2. Department of Chemistry and The State Key Laboratory of Synthetic Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, China
Funder
Imperial College London
Publisher
American Chemical Society (ACS)
Subject
Catalysis,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acscatal.6b00800
Reference28 articles.
1. Direct Generation of Nucleophilic Chiral Palladium Enolate from 1,3-Dicarbonyl Compounds: Catalytic Enantioselective Michael Reaction with Enones
2. Development of catalytic asymmetric reactions via chiral palladium enolates
3. Catalytic Enantioselective Michael Reaction of 1,3-Dicarbonyl Compoundsvia Formation of Chiral Palladium Enolate
4. Development of Catalytic Enantioselective Reactions via Palladium Enolates as Key Intermediates
5. Palladium-catalysed enantioselective α-hydroxylation of β-ketoesters
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