Reduction asymetrique de cetones par des alcoxyaluminohydrures chiraux prepares a partir de l'ephedrine et divers alcools ou phenols achiraux
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference39 articles.
1. Simple Preparation of Optically Active Secondary Alcohols1
2. Asymmetrische Reduktionen, I. Reduktion von 6-Dimethylamino-4.4-diphenyl-hexanon-(3) (Normethadon) mit Komplexen aus Lithiumalanat und isomeren Pinandiolen
3. Asymmetrische Reduktionen, II. Reduktion von (Diphenylmethyl)alkylketonen mit Komplexen aus Lithiumalanat und cis ‐2,3‐Pinandiol
4. Reversal in stereoselectivity depending upon the age of a chiral lithium alkoxyaluminohydride reducing agent
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2. Asymmetric reduction and Meerwein-Ponndorf-Verley reaction of prochiral aromatic ketones in the presence of optically pure 1-aryl-2,2-dimethylpropane-1,3-diols;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
3. The role of tetraalkylammonium salts in the electro-reduction of ketones III. Pinacolization and asymmetric induction;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
4. Asymmetric induction in electropinacolization;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
5. On the Scope of Trimethylaluminium-Promoted 1,2-Additions of ArZnX Reagents to Aldehydes;Chemistry - A European Journal;2009-11-24
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