Asymmetric Diels−Alder Reactions of 2-Pyrones with a Bifunctional Organic Catalyst
- 1 May 2007
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 129 (20) , 6364-6365
- https://doi.org/10.1021/ja070859h
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- Chiral N-Heterocyclic Carbene Catalyzed, Enantioselective Oxodiene Diels−Alder Reactions with Low Catalyst LoadingsJournal of the American Chemical Society, 2006
- Catalytic, Enantioselective Bifunctional Inverse Electron Demand Hetero-Diels−Alder Reactions of Ketene Enolates and o-Benzoquinone DiimidesJournal of the American Chemical Society, 2006
- Total Synthesis of (±)-Haouamine AJournal of the American Chemical Society, 2006
- Enantioselective Nitroaldol Reaction of α-Ketoesters Catalyzed by Cinchona AlkaloidsJournal of the American Chemical Society, 2005
- Catalytic Enantioselective C−C Bond Forming Conjugate Additions with Vinyl SulfonesJournal of the American Chemical Society, 2005
- Single enantiomers from a chiral-alcohol catalystNature, 2003
- New Strategies for Organic Catalysis: The First Highly Enantioselective Organocatalytic Diels−Alder ReactionJournal of the American Chemical Society, 2000
- Asymmetric Base-Catalyzed Diels-Alder Reaction of 3-Hydroxy-2-Pyrone with N-MethylmaleimideChemistry Letters, 1996
- A Base Catalyzed Diels-Alder Reaction of 3-Hydroxy-2-PyroneTetrahedron Letters, 1995
- High-pressure cycloadditions of pyrones: synthesis of highly functionalized six-membered rings by inhibition of carbon dioxide lossThe Journal of Organic Chemistry, 1977