Enantioselective Addition of Diethylzinc to Aromatic Aldehydes Catalysed by Chiral Ligands Derived from L-Hydroxyproline
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397919308013799
Reference32 articles.
1. Enantioselective addition of diethylzinc to benzaldehyde catalyzed by a small amount of chiral 2-amino-1-alcohols
2. Catalytic asymmetric induction. Highly enantioselective addition of dialkylzincs to aldehydes using chiral pyrrolidinylmethanols and their metal salts
3. Polymer-bound N-alkylnorephedrines as efficient chiral catalysts for the enantioselective addition of dialkylzincs to both aromatic and aliphatic aldehydes
4. Catalytic enantioselective synthesis of optically active phthalides
5. Chiral catalysis in the alkylation of aldehydes with diethyl zinc
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1. Enone-promoted decarboxylation of trans-4-hydroxy-l-proline in flow: a side-by-side comparison to batch;Reaction Chemistry & Engineering;2021
2. Enantioselective addition of diethylzinc to aldehydes catalyzed by 5-cis-substituted proline derivatives;Tetrahedron;2019-01
3. ChemInform Abstract: Enantioselective Addition of Diethylzinc to Aromatic Aldehydes Catalyzed by Chiral Ligands Derived from L-Hydroxyproline.;ChemInform;2010-08-19
4. Novel Chiral Catalysts for Asymmetric Addition of Terminal Alkynes to Aldehydes;Current Organic Chemistry;2009-10-01
5. New synthesis of cis-3,4-diaryl-1-tosylpyrrolidines;Tetrahedron Letters;2006-05
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