articleAngewandte Chemie International EditionMay 16, 2008Closed access

Pd II ‐Catalyzed Enantioselective Activation of C(sp 2 )H and C(sp 3 )H Bonds Using Monoprotected Amino Acids as Chiral Ligands

Scripps Research Institute · Brandeis University

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Abstract

The relay of chiral information from the α-carbon atom of the amino acid ligand is believed to be crucial for chiral induction in the PdII-catalyzed enantioselective CH activation/CC coupling reaction of diphenyl(2-pyridyl)methane with boronic acids (see scheme; BQ=benzoquinone). Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2002/2008/z801030_s.pdf or from the author. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.

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Authors

4

Topics & keywords

Keywords
  • Enantioselective synthesis
  • Catalysis
  • Chemistry
  • Amino acid
  • Ligand (biochemistry)
  • Stereochemistry
  • Asymmetric carbon
  • Medicinal chemistry
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