Enantioselective addition of diethylzinc to aldehydes using γ-aminoalcohols derived from α-D-xylose as new chiral catalysts
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Enantioselective addition of organozinc reagents to aldehydes
2. Enantioselective Addition of Organometallic Reagents to Carbonyl Compounds: Chirality Transfer, Multiplication, and Amplification
3. Chiral synthesis via organoboranes. 15. Selective reductions. 42. Asymmetric reduction of representative prochiral ketones with potassium 9-O-(1,2:5,6-di-O-isopropylidene-.alpha.-D-glucofuranosyl)-9-boratabicyclo[3.3.1]nonane
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1. Formation of Alcohols and Phenols by Alkylation of Carbonyl Compounds;Comprehensive Organic Transformations;2018-02-28
2. 1.07 Recent Advances in Organozinc Reagents;Comprehensive Organic Synthesis II;2014
3. ChemInform Abstract: Catalytic Enantioselective Reactions. Part 3. Enantioselective Addition of Diethylzinc to Aldehydes Using γ-Aminoalcohols Derived from α-D-Xylose as New Chiral Catalysts.;ChemInform;2010-08-18
4. Synthesis, resolution, and applications of 3-amino-2,2-dimethyl-1,3-diphenylpropan-1-ol, a conformationally restricted 1,3-aminoalcohol;Tetrahedron;2010-07
5. Chirality Control by Substituents in the Asymmetric Addition of Et2Zn to Aromatic Aldehydes Catalyzed bycis-(1R,2S)-2-Benzamidocyclohexanecarboxylic Acid Derived 1,3-Aminoalcohols;Chinese Journal of Chemistry;2010-01
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