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Enantioselective Atropisomeric Anilides Synthesis via Cu-Catalyzed Intramolecular Adjacent C–N Coupling

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Catalytically asymmetric synthesis of atropisomeric compounds is an important research area in organic synthesis. However, in comparison with C–C atropisomers, the atropisomers caused by the restricted rotation of C–N single… Click to show full abstract

Catalytically asymmetric synthesis of atropisomeric compounds is an important research area in organic synthesis. However, in comparison with C–C atropisomers, the atropisomers caused by the restricted rotation of C–N single bonds have been given less attention because of the limited methods for accessing these compounds. Herein we report a Cu-catalyzed enantioselective intramolecular Ullmann-type amination reaction for the synthesis of C–N atropisomers. The C–N axial chirality was induced highly efficiently by the intramolecular adjacent C–N cross-coupling. The readily prepared N,N′-(cyclohexane-1,2-diyl)dipicolinamides showed high efficacy and stereoinduction (up to 99% ee).

Keywords: synthesis; enantioselective atropisomeric; anilides synthesis; atropisomeric anilides; intramolecular adjacent; synthesis via

Journal Title: ACS Catalysis
Year Published: 2019

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