A

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

  1. RWTH Aachen University

    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

  2. RWTH Aachen University

    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

  3. RWTH Aachen University

    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

  4. RWTH Aachen University

    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

Cited by 13 stored of 13

13 results

No patents citing this paper on Lens.org (checked 2026-10-06).

References 107