Synthesis of C2-symmetrical bis-β-amino alcohols and their application in the enantioselective addition of diethylzinc to aldehydes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference21 articles.
1. Noyori, R. In Asymmetric Catalysis in Organic Synthesis; Wiley: New York, 1994; pp. 255–297
2. Enantioselective Addition of Organometallic Reagents to Carbonyl Compounds: Chirality Transfer, Multiplication, and Amplification
3. Enantioselective addition of organozinc reagents to aldehydes
4. Asymmetric addition of dialkylzincs to benzaldehyde derivatives catalyzed by chiral β-amino alcohols. Evidence for the monomeric alkylzinc aminoalkoxide as catalyst
5. Quantitative Analysis of the Chiral Amplification in the Amino Alcohol-Promoted Asymmetric Alkylation of Aldehydes with Dialkylzincs
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1. Synthesis and Application of a New Class of Planar and Centrally Chiral Ferrocenyl Amino Alcohol Ligands;European Journal of Organic Chemistry;2024-03-06
2. Enantioselective addition of diethylzinc to aromatic aldehydes catalyzed by C2-symmetric chiral diols;Tetrahedron Letters;2014-04
3. The synthesis of chiral amino diol tridentate ligands and their enantioselective induction during the addition of diethylzinc to aldehydes;Tetrahedron: Asymmetry;2014-02
4. Synthesis and Crystal Structure of the Chiral β-amino Alcohol (S)-α,α-diphenyl-2-pyrrolidine Methanol;Journal of Chemical Research;2010-11
5. Modular amino acids and β-amino alcohol-based chiral ligands for enantioselective addition of diethylzinc to aromatic aldehydes;Applied Organometallic Chemistry;2010-10-12
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