159951-54-9Relevant articles and documents
Catalytic, Enantioselective, Inverse Electron-Demand Diels-Alder (IEDDA) Reactions of 3-Carbomethoxy-2-Pyrone (3-CMP)
Marko, Istvan E,Evans, Graham R
, p. 2771 - 2774 (1994)
Cycloaddition reactions between 3-CMP 1 and various vinyl ethers and vinyl sulphides, catalysed by the Yb(OTf)-Binol complex, afford bicyclic lactones 3 in moderate to exellent enantiomeric excesses.
Remarkable effect of basics ligands in the lanthanide-catalysed enantioselective cycloadditions of 3-carbomethoxy-2-pyrone (3-CMP)
Marko, Istvan E.,Chelle-Regnaut, Isabelle,Leroy, Bernard,Warriner, Stuart L.
, p. 4269 - 4272 (2007/10/03)
The key-role of basic ligands in attaining high enantiomeric excess in the lanthanide catalysed asymmetric cycloadditions of 3-CMP is reported. A model, rationalising all our previous observations is discussed.
IMPROVED ENANTIOSELECTIVITY IN THE INVERSE ELECTRON DEMAND DIELS-ALDER CYCLOADDITIONS OF 3-CARBOMETHOXY-2-PYRONE CATALYSED BY CHIRAL YTTERBIUM COMPLEXES
Marko, Istvan E.,Evans, Graham R.,Declercq, Jean-Paul,Feneau-Dupont, Janine,Tinant, Bernard
, p. 295 - 298 (2007/10/02)
When catalysed by the Kobayashi : Yb(OTf)3-Binol complex, vinyl ethers and vinyl sulphides undergo highly enantioselective IEDDA reactions with 3-carbomethoxy-2-pyrone.