An Efficient Asymmetric Synthesis of Atropisomeric 1,1′-Binaphthyls via Nucleophilic Aromatic Substitution Reaction
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/19/5/19_5_807/_pdf
Reference8 articles.
1. Asymmetric synthesis of axially chiral 1,1′:5′,1″- and 1,1′:4′,1″-ternaphthalenes by asymmetric cross-coupling with a chiral ferrocenylphosphine-nickel catalyst
2. Asymmetric Synthesis of Axially Chiral, Unsymmetrical Diphenic Acids via Intramolecular Ullmann Coupling Reaction
3. Enantioselective synthesis of binaphthyls via nucleophilic aromatic substitution on chiral oxazolines
4. Studies in stereochemistry. 47. Asymmetric induction by leaving group in nucleophilic aromatic substitution
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1. Chiral Ligand-Mediated Nucleophilic Aromatic Substitution of Naphthoic Acids: A Fast and Efficient Access to Axially Chiral Biaryls;European Journal of Organic Chemistry;2020-05-18
2. Axially Chiral 1,1'‐Binaphthyl‐2‐Carboxylic Acid (BINA‐Cox) as Ligands for Titanium‐Catalyzed Asymmetric Hydroalkoxylation;European Journal of Organic Chemistry;2020-04
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5. Enantioselective Synthesis of Axially Chiral Hydroxy Carboxylic Acid Derivatives by Rhodium-Catalyzed [2 + 2 + 2] Cycloaddition;The Journal of Organic Chemistry;2011-02-16
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