Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
68269 | Journal of Molecular Catalysis A: Chemical | 2007 | 5 Pages |
Abstract
The catalytic enantioselective arylation of several aldehydes using arylboronic acids as the source of transferable aryl groups is described; the reaction is found to proceed in excellent yields and high enantioselectivities (up to 96% ee) in the presence of a chiral amino alcohol derived from ephedrines and congeners.
Graphical abstractThe catalytic enantioselective arylation of several aldehydes using arylboronic acids as the source of transferable aryl groups is described; the reaction is found to proceed in excellent yields and high enantioselectivities (up to 96% ee) in the presence of a chiral amino alcohol derived from ephedrines and congeners. Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Catalysis
Authors
Marcio W. Paixao, Marcelo de Godoi, Cristiano R.B. Rhoden, Bernhard Westermann, Ludger A. Wessjohann, Diogo S. Lüdtke, Antonio L. Braga,