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. |
| |
Keywords: | |
本文献已被 PubMed 等数据库收录! |
|