Catalysis of the specific michael addition : The example of acrylate acceptors
- 1 January 1989
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 30 (30) , 3969-3972
- https://doi.org/10.1016/s0040-4039(00)99297-9
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Catalysis of Friedel‐Crafts Alkylation by a Montmorillonite Doped with Transition‐Metal CationsHelvetica Chimica Acta, 1987
- Theoretical studies of conformations of acrolein, acrylic acid, methyl acrylate, and their Lewis acid complexesJournal of the American Chemical Society, 1987
- Intramolecular 1,3-diyl trapping reactions. A formal total synthesis of (.+-.)-coriolinThe Journal of Organic Chemistry, 1985
- Acyclic stereoselection. 31. Stereoselection in the Michael addition reaction. 3. Relationship between ester enolate geometry and adduct stereochemistry in the kinetic Michael reaction of lithium enolates with enonesThe Journal of Organic Chemistry, 1985
- Catalysis of the Michael reactionTetrahedron Letters, 1985
- Ph3P-(PyS)2-CH3CN as an excellent condensing system for .beta.-lactam formation from .beta.-amino acidsJournal of the American Chemical Society, 1981
- Reduction de la cyclohexen-2 one par LiAlH4 et LiBH4 : Inversion de regioselectivite par addition de cryptantsTetrahedron Letters, 1978
- A novel stereospecific alkenyl-alkenyl cross-coupling by a palladium- or nickel-catalyzed reaction of alkenylalanes with alkenyl halidesJournal of the American Chemical Society, 1976
- Regioselectivite sous controle d'interactions de charges ou d'interactions orbitalairesTetrahedron, 1975
- Ueber die Addition von Natriumacetessig‐ und Natriummalonsäureäthern zu den Aethern ungesättigter SäurenJournal für Praktische Chemie, 1887