Synfacts 2008(1): 0068-0068  
DOI: 10.1055/s-2007-991483
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag Stuttgart · New York

Highly Enantioselective Hydrogenation of Tetrasubstituted Olefins

Contributor(s): Mark Lautens, Michael Langer
M. G. Schrems, E. Neumann, A. Pfaltz*
University of Basel, Switzerland
Further Information

Publication History

Publication Date:
18 December 2007 (online)

Significance

The hydrogenation of tetrasubstituted olefins remains challenging despite the many examples of hydrogenation catalysts described in recent years. Few catalysts have been reported that can convert highly substituted olefins under mild conditions in high enantioselecti­vities. Pfaltz and co-workers report the synthesis of novel P,N-ligands based on the phosphino oxazoline motif and the use of the corresponding iridium complexes in the asymmetric hydrogenation of unfunctionalized, tetrasubstituted olefins.