Chiral enolates for highly stereoselective aldol reactions—Scope and limitations
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference37 articles.
1. For recent developments in Cu-catalyzed conjugate addition reactions, see
2. Enantioselective Copper-Catalyzed Conjugate Addition and Allylic Substitution Reactions
3. Recent advances in enantioselective copper-catalyzed 1,4-addition
4. Recent Advances in Metal-Catalyzed Asymmetric Conjugate Additions
5. Recent Advances in Catalytic Enantioselective Michael Additions
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2. Asymmetric Transition-Metal Catalysis in the Formation and Functionalization of Metal Enolates;ACS Catalysis;2019-02-25
3. Activation of Marginally Reactive Boron Enolates by MeLi for the Formation of Enol Phosphates and Synthesis of the Δ9-THC Intermediate;The Journal of Organic Chemistry;2015-09-08
4. Copper-Catalyzed Asymmetric Conjugate Addition;Copper-Catalyzed Asymmetric Synthesis;2014-01-03
5. First Tandem Asymmetric Conjugate Addition of Alkenyl Nucleophiles and Silyl Trapping of the Intermediate Enolates;Advanced Synthesis & Catalysis;2013-09-10
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