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Cite Publication Date: Nov 5, 2012 | |
 Citations: 238 |
Affiliation: Scripps Research Institute
Pd(II) insertion into β-methylene C(sp(3))-H bonds was enabled by a mutually repulsive and electron-rich quinoline ligand. Ligand tuning led to the development of a method that allows for installation of an aryl group on a range of acyclic and cyclic amides containing β-methylene C(sp(3))-H bonds.
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