Ni(II)-catalyzed Michael additions. Part 2: Dynamic kinetic resolution in the reduction of chiral α-hydrazino-β-ketoacid derivatives
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference24 articles.
1. Nickel(II)-catalyzed Michael additions. Formation of quaternary centers and diastereoselective addition of enantiopure N -acetoacetyl-4-benzyloxazolidin-2-one
2. Transition-Metal Catalysis of the Michael Reaction of 1,3-Dicarbonyl Compounds and Acceptor-Activated Alkenes
3. Enantioselective Conjugate Additions
4. Towards Perfect Asymmetric Catalysis: Additives and Cocatalysts
5. Construction of Quaternary Stereocenters by Nickel-Catalysis of Asymmetric Michael Reactions
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1. Saturated Heterocycles as Chiral Auxiliaries;Chiral Building Blocks in Asymmetric Synthesis;2022-08-12
2. Recent developments in enantioselective nickel(ii)-catalyzed conjugate additions;Organic Chemistry Frontiers;2022
3. The Developing Concept of Bifunctional Catalysis with Transition Metal N‐Heterocyclic Carbene Complexes;European Journal of Inorganic Chemistry;2016-03-09
4. Recent Developments in Enantioselective Nickel(II)-Catalyzed Conjugate Additions;Advanced Synthesis & Catalysis;2015-09-10
5. Gold nanoparticles decorated with a cinchonine organocatalyst: application in the asymmetric α-amination of β-ketoesters;New J. Chem.;2014
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