Asymmetric Aza‐Morita–Baylis-Hillman Reaction of N‐Sulfonated Imines with Activated Olefins Catalyzed by Chiral Phosphine Lewis Bases Bearing Multiple Phenol Groups
- 5 May 2006
- journal article
- research article
- Published by Wiley in Advanced Synthesis & Catalysis
- Vol. 348 (7-8) , 973-979
- https://doi.org/10.1002/adsc.200505476
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Bifunctional Organocatalysts for Enantioselective aza-Morita−Baylis−Hillman ReactionJournal of the American Chemical Society, 2005
- Chiral Phosphine Lewis Bases Catalyzed Asymmetric aza-Baylis−Hillman Reaction of N-Sulfonated Imines with Activated OlefinsJournal of the American Chemical Society, 2005
- β-Isocupreidine-Catalyzed Asymmetric Baylis−Hillman Reaction of IminesOrganic Letters, 2003
- Chiral quinuclidine-based amine catalysts for the asymmetric one-pot, three-component aza-Baylis–Hillman reactionTetrahedron Letters, 2003
- Recent Advances in the Baylis−Hillman Reaction and ApplicationsChemical Reviews, 2003
- Catalytic, Asymmetric Baylis–Hillman Reaction of Imines with Methyl Vinyl Ketone and Methyl AcrylateAngewandte Chemie International Edition in English, 2002
- Recent Progress in the Morita-Baylis-Hillman Reactions.Journal of Synthetic Organic Chemistry, Japan, 2002
- New Strategies for the Development of an Asymmetric Version of the Baylis–Hillman ReactionPublished by Wiley ,2000
- The Baylis-Hillman reaction: A novel carbon-carbon bond forming reactionTetrahedron, 1996
- Synthetic potential of the tertiary-amine-catalysed reaction of activated vinyl carbanions with aldehydesTetrahedron, 1988