Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1323177 | Journal of Organometallic Chemistry | 2012 | 9 Pages |
The asymmetric hydrogenation of olefins is a tremendously powerful tool used to synthesize chiral molecules. The field was pioneered using rhodium- and ruthenium- based catalysts; however, catalysts based on both of these metals suffer from limitations, such as the need for directing substituents near or even adjacent to the olefin. Iridium-based catalysts do not suffer from this flaw and can thus hydrogenate a wide variety of olefins, including some tetra substituted ones. It is also possible for iridium-based catalysts to hydrogenate hetero-π bonds such as those found in hetero-aromatic rings. This review summarizes the contributions made to this field by our research group over the past few years.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► We summarize works done by our group using Iridium catalyzed asymmetric hydrogenation. ► We present a brief summary of work done in the field of Iridium catalysis. ► We expand upon the current scope of alkene hydrogenation.