A New Cationic, Chiral Catalyst for Highly Enantioselective Diels−Alder Reactions
- 18 June 2003
- journal article
- research article
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 5 (14) , 2465-2467
- https://doi.org/10.1021/ol034706k
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Triflimide Activation of a Chiral Oxazaborolidine Leads to a More General Catalytic System for Enantioselective Diels−Alder AdditionJournal of the American Chemical Society, 2003
- The formyl C–H⋯O hydrogen bond as a critical factor in enantioselective Lewis-acid catalyzed reactions of aldehydesChemical Communications, 2001
- A Novel Chiral Super-Lewis Acidic Catalyst for Enantioselective SynthesisJournal of the American Chemical Society, 1996
- The osmium-catalyzed asymmetric dihydroxylation: a new ligand class and a process improvementThe Journal of Organic Chemistry, 1992
- New method for coupling allylic halides: use of telluride(2-) ion speciesThe Journal of Organic Chemistry, 1982