Asymmetric 1,3-Dipolar Cycloaddition of Nitrile Oxides Generated in situ by Direct Oxidation of Aldoximes
- 1 November 2002
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 31 (11) , 1112-1113
- https://doi.org/10.1246/cl.2002.1112
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Enantioselective 1,3-Dipolar Cycloaddition of Nitrones Catalyzed by Optically Active Cationic Cobalt(III) ComplexesOrganic Letters, 2002
- Iron and Ruthenium Lewis Acid Catalyzed Asymmetric 1,3-Dipolar Cycloaddition Reactions between Nitrones and EnalsJournal of the American Chemical Society, 2002
- Chiral bis(trialkylsiloxymethyloxazolinyl)pyridine ligands. Highly enantioselective 1,3-dipolar cycloaddition reactionsTetrahedron, 2002
- New Strategies for Organic Catalysis: The First Enantioselective Organocatalytic 1,3-Dipolar CycloadditionJournal of the American Chemical Society, 2000
- Metal ion-mediated diastereoface-selective 1,3-dipolar cycloaddition of nitrile oxides with dipolarophiles bearing an oxazolidinone chiral auxiliaryTetrahedron Letters, 2000
- Synthesis of Hydroximoyl Chlorides from Aldoximes and Benzyltrimethylammonium Tetrachloroiodate (BTMA ICl4)Tetrahedron, 2000
- Enantioselective Synthesis of Lythraceae Alkaloid Lasubine II via Optically Active 2-IsoxazolineHETEROCYCLES, 2000
- Asymmetric 1,3-Dipolar Cycloaddition ReactionsChemical Reviews, 1998
- A Simple Regioselective Synthesis of Hydroximinoyl Chlorides (Nitrile Oxide Precursors)Synthetic Communications, 1986
- A particularly convenient preparation of benzohydroximinoyl chlorides (nitrile oxide precursors)The Journal of Organic Chemistry, 1980