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Samarium-promoted coupling of 1,10-phenanthroline with carbonyl compounds for synthesis of new ligands
Authors:Weitgenant Jeremy A  Mortison Jonathan D  O'Neill David J  Mowery Brendan  Puranen Anders  Helquist Paul
Affiliation:Department of Chemistry and Biochemistry and Walther Cancer Research Center, 251 Nieuwland Science Hall, University of Notre Dame, Notre Dame, Indiana 46556, USA.
Abstract:1,10-Phenanthroline reacts with aldehydes and ketones in the presence of samarium diiodide to produce 2-(1-hydroxyalkyl)-1,10-phenanthrolines. The hydroxyalkyl substituent can be functionalized in numerous ways or removed to permit further ligand variation. The carbonyl coupling reaction can also be repeated to provide 2,9-disubstituted phenanthrolines. Taken together, these operations provide ready access to a large number of phenanthroline derivatives to serve as ligand libraries for catalyst exploration.
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