2.08 The Aldol Reaction: Group I and Group II Enolates
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Publisher
Elsevier
Reference241 articles.
1. β-HYDROXY ESTERS FROM KETONES AND ESTERS
2. Aldol Condensation of Esters with Ketones or Aldehydes to Form β-Hydroxy Esters by Lithium Amide. Comparison with the Reformatsky Reaction1
3. Aldol Condensation of Ethyl Acetate with Ketones to Form β-Hydroxy Esters by Lithium Amide1
4. Reaction of 9-Bromomethylenefluorene with Potassium Amide in Liquid Ammonia. Dimerization1
5. Synthesis of β-Hydroxy Esters from Ethyl Acetate and Ketones or Aldehydes by Means of Lithium Amide. Some Results with Other Esters1
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1. Catalytic Enantioselective Hydrovinylation of Trialkylsilyloxy and Acetoxy-1,3-Dienes: Cationic Co(I) Complexes for the Synthesis of Chiral Enolate Surrogates and Their Applications for Synthesis of Ketones and Cross-Coupling Reagents in High Enantiomeric Purity;ACS Catalysis;2022-04-14
2. Glycerol Electrocatalytic Reduction Using an Activated Carbon Composite Electrode: Understanding the Reaction Mechanisms and an Optimization Study;Frontiers in Chemistry;2022-02-25
3. Catalytic Enantioselective Alkylation of Prochiral Enolates;Chemical Reviews;2021-07-26
4. NHC-Ni catalyzed enantioselective synthesis of 1,4-dienes by cross-hydroalkenylation of cyclic 1,3-dienes and heterosubstituted terminal olefins;Nature Communications;2020-05-08
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