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Synfacts 2007(5): 0511-0511
DOI: 10.1055/s-2007-968449
DOI: 10.1055/s-2007-968449
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag Stuttgart · New York
Enantioselective Michael Additions of Indole to Benzylidene Malonates
R. Rasappan, M. Hager, A Gissibl, O. Reiser*
Universität Regensburg, Germany
Further Information
Publication History
Publication Date:
24 April 2007 (online)
Significance
The reported study contradicts the general trends previously observed in Cu-catalyzed reactions. Indeed, background reactions often occur faster with a ligand-free metal than with coordinated species, leading to erosion of enantioselectivity. Thus, an excess of ligand is usually used. Previous studies had concluded that BOX ligands like 4 were unsuitable for the above reaction (79% ee). It was now shown that, for the specific system presented, the BOX ligands are among the best ligands (99% ee), provided that the ligand is not used in excess versus the metal catalyst. The parent ligand 5 increased the reactivity, giving the desired chiral adduct 3 in 97% yield (instead of 89% with 4).