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 CH activation/CC 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
4Topics & keywords
Topics
Keywords
- Enantioselective synthesis
- Catalysis
- Chemistry
- Amino acid
- Ligand (biochemistry)
- Stereochemistry
- Asymmetric carbon
- Medicinal chemistry
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