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      Highly Enantioselective Kinetic Resolution of Axially Chiral BINAM Derivatives Catalyzed by a Brønsted Acid

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          Abstract

          A highly efficient strategy for the kinetic resolution of axially chiral BINAM derivatives involving a chiral Brønsted acid-catalyzed imine formation and transfer hydrogenation cascade process was developed. The kinetic resolution provides a convenient route to chiral BINAM derivatives in high yields with excellent enantioselectivities.

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          Stronger Brønsted acids.

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            Large-scale applications of transition metal-catalyzed couplings for the synthesis of pharmaceuticals.

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              Chiral Phosphoric Acids as Versatile Catalysts for Enantioselective Transformations

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                Author and article information

                Journal
                Angewandte Chemie International Edition
                Angew. Chem. Int. Ed.
                Wiley-Blackwell
                14337851
                April 01 2014
                April 01 2014
                : 53
                : 14
                : 3684-3687
                Article
                10.1002/anie.201310562
                24591330
                eea362b0-736f-457f-b351-c7d568f0832f
                © 2014

                http://doi.wiley.com/10.1002/tdm_license_1.1

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