Asymetric alkylation of carbonyl compounds with chiral lithium alkoxy-tributyl aluminate.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. Stereoselectivite et regioselectivite de l'alkylation d'epoxydes par les “ates” complexes : Tetrabutylaluminate de lithium et tetraethylaluminate de sodium.
2. Alkylation stereoselective de composes carbonyles par le “ate” complexe : tetraethylaluminate de sodium. Activation catalytique par le chlorure de nickel
3. Reduction asymetrique de cetones par des alcoxyaluminohydrures chiraux prepares a partir de l'ephedrine et divers alcools ou phenols achiraux
4. Asymmetric Solvent Catalysis;N,N,N′,N′-Tetramethyl-2,3-dimethoxy-1,4-butanediamine, a New Chiral Medium
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1. Chiral Lithium Amido Zincates for Enantioselective 1,2-Additions: Auto-assembling Reagents Involving a Fully Recyclable Ligand;Chemistry - A European Journal;2018-05-29
2. Solution Structures of Lithium Amino Alkoxides Used in Highly Enantioselective 1,2-Additions;Journal of the American Chemical Society;2014-02-05
3. Mixed AggregAte (MAA): A Single Concept for All Dipolar Organometallic Aggregates. 2. Syntheses and Reactivities of Homo/HeteroMAAs;Chemical Reviews;2013-08-16
4. Lithium tetrabutylaluminate-N-Methylephedrine 1;Fieser and Fieser's Reagents for Organic Synthesis;2006-12-15
5. (1R,2S)-N-Methylephedrine;Encyclopedia of Reagents for Organic Synthesis;2001-04-15
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