Enantioselective Desymmetrization of Prochiral Cyclohexanones via Organocatalytic Intramolecular Michael Additions To A,B-Unsaturated Esters

Enantioselective Desymmetrization of Prochiral Cyclohexanones via Organocatalytic Intramolecular Michael Additions To A,B-Unsaturated Esters.

Gammack-Yamagata, A. D.; Datta, S.; Jackson, K. E.; Stegbauer, L.; Paton, R. S.; Dixon, D. J. Angew. Chem. Int. Ed. 2015, 127, 4981–4985

You might also like
Catalytic Control in Cyclizations: from Computational Mechanistic Understanding to Selectivity Prediction
The True Catalyst Revealed: the Intervention of Chiral Ca and Mg Phosphates in Brønsted Acid Promoted Asymmetric Mannich Reactions
C-Alkylation of Chiral Tropane- and Homotropane-Derived Enamines
Computational Organic Chemistry
Origins of Asymmetric Phosphazene Organocatalysis: Computations Reveal a Common Mechanism for Nitro- and Phospho-Aldol Additions
Hydrogen Bonding Phase-Transfer Catalysis with Potassium Fluoride: Enantioselective Synthesis of Beta-Fluoroamines
Asymmetric Nucleophilic Fluorination Under Hydrogen Bonding Phase Transfer Catalysis
Catalytic Enantioselective Synthesis of Indanes via Cation-Directed 5-Endo-Trig Cyclization