Asymmetric addition of n-butyllithium to aldehydes: new insights into the reactivity and enantioselectivity of the chiral amino ether accelerated reaction-Reference-Cited by-同舟云学术

Asymmetric addition of n-butyllithium to aldehydes: new insights into the reactivity and enantioselectivity of the chiral amino ether accelerated reaction

Published:2002-06 Issue:23 Volume:58 Page:4717-4725
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Granander Johan,Sott Richard,Hilmersson Göran

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference38 articles.

1. Asymmetric carbinol synthesis by means of (−)-sparteine-modified organometallic reagents

2. Enantioface-differentiating (asymmetric) addition of alkyllithium and dialkylmagnesium to aldehydes by using (2S,2'S)-2-hydroxymethyl-1-[(1-alkylpyrrolidin-2-yl)methyl]pyrrolidines as chiral ligands

3. Chiral catalysis of additions of alkyllithiums to aldehydes

4. Enantioselective addition of n-butyllithium to benzaldehyde in the presence of chiral lithium amides

5. A Multinuclear NMR Study of a Chiral Lithium Amide with an Intramolecular Chelating Methoxy Group in Coordinating Solvents at the Slow Ligand Exchange Limit

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