1,1′-Binaphthylazepine-based ligands for the enantioselective dialkylzinc addition to aromatic aldehydes
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference83 articles.
1. Enantioselective Addition of Organometallic Reagents to Carbonyl Compounds: Chirality Transfer, Multiplication, and Amplification
2. Enantioselective addition of organozinc reagents to aldehydes
3. Catalytic Asymmetric Organozinc Additions to Carbonyl Compounds
4. Enantioselective addition of dialkylzincs to aldehydes promoted by chiral amino alcohols. Mechanism and nonlinear effect
5. An Ab Initio Molecular Orbital Study on the Amino Alcohol-Promoted Reaction of Dialkylzincs and Aldehydes
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1. 5,5,7,7-Tetrametyl-6,7-dihydro-5H-dibenzo[c,e]azepine;Molbank;2023-01-16
2. New Catalysts Derived from Natural Products as Highly Stereoselective Chiral Inductors for Diethylzinc Addition to Aromatic Aldehydes;Journal of the Brazilian Chemical Society;2023
3. Porous aromatic frameworks containing binaphthyl-dihydroazepine units (cBAPAFs) as catalytic supports for asymmetric reactions;Journal of Catalysis;2022-09
4. Synthesis and Stereochemical Characterization of a Novel Chiral α-Tetrazole Binaphthylazepine Organocatalyst;Molecules;2022-08-11
5. Deciphering the mechanism behind efficient enantioselective ethylation with thiazolidine‐based amino alcohols;Applied Organometallic Chemistry;2021-12-30
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