4.4 Article

Chiral imidates as a new class of nitrogen-based chiral ligands: synthesis and catalytic activity in asymmetric aziridinations and diethylzinc additions

Journal

TETRAHEDRON
Volume 65, Issue 43, Pages 8879-8884

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2009.08.028

Keywords

Chiral imidates; Transition metal catalysis; Asymmetric aziridination; Asymmetric diethylzinc additions

Funding

  1. Ghent University
  2. COST-Chemistry

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Chiral imidates were efficiently synthesized in one step and with high yields (seven examples). These chiral imidates were used as ligands in the Cu(I)-catalyzed asymmetric aziridination of methyl cinnamate and in the asymmetric diethylzinc additions to benzaldehyde as a proof of principle. The imidate catalyst system showed high catalytic activities and induced encouraging selectivities. An X-ray structure analysis of an imidate-Cu(I) complex is included, showing a distorted tetrahedral arrangement with two bidentate ligand molecules surrounding the metal. (c) 2009 Elsevier Ltd. All rights reserved.

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