Chirality Control by Substituents in the Asymmetric Addition of Et2Zn to Aromatic Aldehydes Catalyzed bycis-(1R,2S)-2-Benzamidocyclohexanecarboxylic Acid Derived 1,3-Aminoalcohols
Author:
Publisher
Wiley
Subject
General Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/cjoc.201090036/fullpdf
Reference66 articles.
1. Enantioselective addition of diethylzinc to benzaldehyde catalyzed by a small amount of chiral 2-amino-1-alcohols
2. The importance of nitrogen substituents in chiral amino thiol ligands for the asymmetric addition of diethylzinc to aromatic aldehydes
3. An l-proline-based β-amino tertiary thiol: synthesis and use as a catalyst in the enantioselective addition of diethylzinc to aldehydes
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3. Synthesis of Chiral 1,3-Diamines Derived from cis-2-Benzamidocyclohexanecarboxylic Acid and Their Application in the Cu-Catalyzed Enantioselective Henry Reaction;Chemistry - A European Journal;2011-10-25
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