α-Hydroxy carboxylic acids: new ligands for diethylzinc additions to aldehydes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference20 articles.
1. Catalytic asymmetric induction. Highly enantioselective addition of dialkylzincs to aldehydes
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3. (b) Pu, L.; Yu, H.-B. Chem. Rev. 2001, 101, 757–824.
4. Enantioselective Addition of Diethylzinc to Aldehydes Catalyzed by A Drug-Unrelated Chiral Amino Thiol and the Corresponding Disulfide
5. Chiral ligands containing heteroatoms. 14. 1,3-oxazolidinyl methanols as chiral catalysts in the enantioselective addition of diethylzinc to aldehydes
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2. Chiral P,N‐ligands for the highly enantioselective addition of diethylzinc to aromatic aldehydes;Applied Organometallic Chemistry;2019-08-05
3. Kinetic Resolution of α-Hydroxy Carboxylic Acid Derivatives Based on Chiral Recognition of Substrate–Cocatalyst Complex;Springer Theses;2019
4. Readily Available Highly Active [Ti]-Adamantyl-BINOL Catalysts for the Enantioselective Alkylation of Aldehydes;ACS Omega;2018-01-30
5. Metal-free one-pot α-carboxylation of primary alcohols;Organic & Biomolecular Chemistry;2016
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