Construction of contiguous chiral tertiary carbon centers by enantioselective Michael reaction of ketone lithium enolates using a chiral amine ligand
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Chiral crown complexes catalyse Michael addition reactions to give adducts in high optical yields
2. A Catalytic Asymmetric Michael Reaction of Silyl Enol Ethers with α,β-Unsaturated Ketones Using a Chiral Titanium Oxide
3. Asymmetric Michael reaction of an α-cyano Weinreb amide catalyzed by a rhodium complex with trans-chelating chiral diphosphine PhTRAP
4. Self-Assembly of Heterobimetallic Complexes and Reactive Nucleophiles: A General Strategy for the Activation of Asymmetric Reactions Promoted by Heterobimetallic Catalysts
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1. Conjugate Addition to α,β-Unsaturated Nitriles, Carboxylic Acids, and Derivatives;Comprehensive Organic Transformations;2018-02-28
2. In situ formed acetals facilitated direct Michael addition of unactivated ketones;New Journal of Chemistry;2017
3. Polyfunctional β-Dicarbonyl Compounds by Michael Addition Reactions of Ester Enolates to α-Benzylidene and α-Alkylidene-β-dicarbonyl Compounds;European Journal of Organic Chemistry;2012-05-09
4. ChemInform Abstract: Construction of Contiguous Chiral Tertiary Carbon Centers by Enantioselective Michael Reaction of Ketone Lithium Enolates Using a Chiral Amine Ligand.;ChemInform;2010-08-03
5. Aspects of the Synthesis, Structure and Reactivity of Lithium Enolates;PATAI'S Chemistry of Functional Groups;2009-12-15
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