4.7 Article

Peptide-catalyzed kinetic resolution of planar-chiral metallocenes

Journal

CHEMICAL COMMUNICATIONS
Volume 50, Issue 58, Pages 7893-7896

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c4cc03266g

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Funding

  1. JSPS [23550116]
  2. MEXT [24105506]
  3. Grants-in-Aid for Scientific Research [23550116, 26105710, 24105506] Funding Source: KAKEN

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Kinetic resolution of racemic planar-chiral metallocenes was performed through the conjugate addition of a nucleophile to the enal part of substrates. While no enantiomeric discrimination was found with low-molecular-weight organocatalysts, a properly designed resin-supported peptide catalyzed the reaction in a highly selective manner.

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