Atroposelective Chan–Evans–Lam Amination
Chemistry - A European Journal, vol. 30, pp. e202304378
Abstract
The synthetic control of atropoisomerism along C-N bonds is a major challenge, and methods that allow C-N atroposelective bond formation are rare. This is a problem because each atropoisomer can feature starkly differentiated biological properties. Yet, among the three most practical and applicable classical amination methods available: 1) the Cu-catalyzed Ullmann-Goldberg reaction, 2) the Pd-catalyzed Buchwald-Hartwig reaction, and 3) the Cu-catalyzed Chan-Evans-Lam reaction, none has truly been rendered atroposelective at the newly formed C-N bond. The first ever Chan-Evans-Lam atroposelective amination is herein described with a simple copper catalyst and newly designed PyrOx chiral ligand. This method should find important applications in asymmetric synthesis, in particular for medicinal chemistry.
Authors 4
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Affiliation as printed
Institute of Organic Chemistry RWTH Aachen University Landoltweg 1 52074 Aachen Germany
Institute of Organic Chemistry RWTH Aachen University Landoltweg 1 52074 Aachen Germany
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Affiliation as printed
Institute of Organic Chemistry RWTH Aachen University Landoltweg 1 52074 Aachen Germany
Institute of Organic Chemistry RWTH Aachen University Landoltweg 1 52074 Aachen Germany
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Affiliation as printed
Institute of Organic Chemistry RWTH Aachen University Landoltweg 1 52074 Aachen Germany
Institute of Organic Chemistry RWTH Aachen University Landoltweg 1 52074 Aachen Germany
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Affiliation as printed
Institute of Organic Chemistry RWTH Aachen University Landoltweg 1 52074 Aachen Germany
RWTH Aachen University, Institute of Organic Chemistry, Landoltweg 1, 52074 Aachen, GERMANY
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