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Peptide-catalyzed kinetic resolution of planar-chiral metallocenes. | LitMetric

Peptide-catalyzed kinetic resolution of planar-chiral metallocenes.

Chem Commun (Camb)

Institute of Industrial Science, University of Tokyo, 4-6-1 Komaba, Meguro-ku, Tokyo 153-8505, Japan.

Published: July 2014

AI Article Synopsis

  • Kinetic resolution of racemic planar-chiral metallocenes was achieved using a nucleophile in the conjugate addition to the enal portion of the substrates.
  • Low-molecular-weight organocatalysts did not show any enantiomeric discrimination in the process.
  • A specially designed resin-supported peptide was able to catalyze the reaction with high selectivity.

Article Abstract

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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Source
http://dx.doi.org/10.1039/c4cc03266gDOI Listing

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