Highly Enantioselective (S)-Homoproline-catalyzed Michael Addition Reactions of Ketones to β-Nitrostyrenes
- 4 June 2005
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 34 (7) , 962-963
- https://doi.org/10.1246/cl.2005.962
Abstract
No abstract availableThis publication has 32 references indexed in Scilit:
- Proline-catalyzed asymmetric aldol reactions of tetrahydro-4H-thiopyran-4-one with aldehydesTetrahedron Letters, 2004
- Benzoimidazole–pyrrolidine (BIP), a highly reactive chiral organocatalyst for aldol processTetrahedron Letters, 2004
- Amino alcohol catalyzed direct asymmetric aldol reactions: enantioselective synthesis of anti -α-fluoro-β-hydroxy ketonesTetrahedron Letters, 2004
- Asymmetric Direct Aldol Reaction Assisted by Water and a Proline‐Derived Tetrazole CatalystAngewandte Chemie International Edition in English, 2004
- Catalytic Direct Asymmetric Michael Reactions: Taming Naked Aldehyde DonorsOrganic Letters, 2001
- Efficient Proline-Catalyzed Michael Additions of Unmodified Ketones to Nitro OlefinsOrganic Letters, 2001
- Catalytic enantioselective direct Michael additions of ketones to alkylidene malonatesTetrahedron Letters, 2001
- Amino Acid Catalyzed Direct Asymmetric Aldol Reactions: A Bioorganic Approach to Catalytic Asymmetric Carbon−Carbon Bond-Forming ReactionsJournal of the American Chemical Society, 2001
- Proline-Catalyzed Asymmetric Aldol Reactions between Ketones and α-Unsubstituted AldehydesOrganic Letters, 2001
- Proline-Catalyzed Direct Asymmetric Aldol ReactionsJournal of the American Chemical Society, 2000