Enantioselective Michael Addition to α,β-Unsaturated Imides Catalyzed by a Bifunctional Organocatalyst
- 17 June 2005
- journal article
- zuschrift
- Published by Wiley in Angewandte Chemie
- Vol. 117 (26), 4100-4103
- https://doi.org/10.1002/ange.200500459
Abstract
No abstract availableKeywords
This publication has 87 references indexed in Scilit:
- Influence of ionic liquids on the phase transfer-catalysed enantioselective Michael reactionTetrahedron Letters, 2003
- Enantioselective Michael Reaction Catalyzed by Well-Defined Chiral Ru Amido Complexes: Isolation and Characterization of the Catalyst Intermediate, Ru Malonato Complex Having a Metal−Carbon BondJournal of the American Chemical Society, 2003
- Novel heterobimetallic catalysts for asymmetric Michael reactionsTetrahedron: Asymmetry, 2003
- Rhodium-Catalyzed Carbon−Carbon Bond Forming Reactions of Organometallic CompoundsChemical Reviews, 2002
- Highly enantioselective catalytic Michael reaction of α-substituted malonates using La-linked-BINOL complex in the presence of HFIP (1,1,1,3,3,3-hexafluoroisopropanol)Tetrahedron Letters, 2002
- Amino acids and peptides as asymmetric organocatalystsTetrahedron, 2002
- Recent Advances in Catalytic Enantioselective Michael AdditionsSynthesis, 2001
- Enantioselektiver Aufbau quartärer StereozentrenAngewandte Chemie, 2001
- Enantioselective Conjugate AdditionsTetrahedron, 2000
- Control of Asymmetry Through Conjugate Addition ReactionsEuropean Journal of Organic Chemistry, 1998