4.3 Article

Metal-controlled Reversal of Enantioselectivity in Catalyzed Asymmetric Ring-opening Reactions of meso-Epoxides in Water

Journal

CHEMISTRY LETTERS
Volume 38, Issue 9, Pages 904-905

Publisher

CHEMICAL SOC JAPAN
DOI: 10.1246/cl.2009.904

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Funding

  1. Japan Society for the Promotion of Science (JSPS)
  2. Global COE Program
  3. University of Tokyo, MEXT, Japan

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Reversal of enantioselectivity in Cu-chiral bipyridine catalyzed asymmetric ring-opening reactions of meso-epoxides with indole and aniline derivatives was observed compared to Sc-chiral bipyridine catalyzed reactions, where the same chiral ligand was used. It was revealed from X-ray crystal structural analysis that a square pyramidal structure for the Cu(II) complex and a pentagonal bipyramidal structure for the Sc(III) complex were formed, which could explain the reversal of the enantioselectivity.

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