4.8 Article

Enantioselective Generation of Adjacent Stereocenters in a Copper-Catalyzed Three-Component Coupling of Imines, Allenes, and Diboranes

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 55, Issue 39, Pages 11912-11916

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201606710

Keywords

amines; asymmetric catalysis; boron; copper; multicomponent reactions

Funding

  1. University of Manchester
  2. SCI
  3. BBSRC
  4. EPSRC
  5. EPSRC [EP/E021220/1, EP/P001386/1] Funding Source: UKRI
  6. Biotechnology and Biological Sciences Research Council [1626760] Funding Source: researchfish
  7. Engineering and Physical Sciences Research Council [1653669, EP/E021220/1, EP/P001386/1, 1093835] Funding Source: researchfish

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A highly enantio-and diastereoselective copper-catalyzed three-component coupling affords the first general synthesis of homoallylic amines bearing adjacent stereocenters from achiral starting materials. The method utilizes a commercially available NHC ligand and copper source, operates at ambient temperature, couples readily available simple imines, allenes, and diboranes, and yields high-value homoallylic amines that exhibit versatile amino, alkenyl, and boryl units.

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