On the mechanism of the formation of s(−)-(1, 1'-binaphthalene)-2,2'-diol via copper(II)amine complexes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference28 articles.
1. Highly enantioselective reduction of alkynyl ketones by a binaphthol-modified aluminum hydride reagent. Asymmetric synthesis of some insect pheromones
2. Asymmetric synthesis via axially dissymetric molecules. 2. A highly efficient synthesis of prostaglandin intermediates possessing the 15S configuration
3. Reduction asymetrique de cetones par des alcoxyaluminohydrures chiraux prepares a partir de l'ephedrine et divers alcools ou phenols achiraux
4. Asymmetric Synthesis of Axially Dissymmetric 1,1′-Binaphthylsviaan Intramolecular Ullmann Coupling Reaction of (R)- and (S)-2,2′-Bis(1-bromo-2-naphthylcarbonyloxy)-1,1′-binaphthyl
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1. Chiral α-Aminophosphonates as Ligands in Copper-Catalyzed Asymmetric Oxidative Coupling of 2-Naphthols;Organic Letters;2024-06-17
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