Concepedia

Highly diastereoselective Michael reaction of ( S )-mandelic acid enolate. Chiral benzoyl carbanion equivalent through an oxidative decarboxylation of α-hydroxyacids

Gonzalo Blay, Isabel Fernández, Belén Monje, José R. Pedro, Rafael Ruiz-Garcı́a

Tetrahedron Letters · 2002 · 16 citations · 14 references

DOI

Concepts

References

14

Recent Advances in Catalytic Enantioselective Michael Additions

Norbert Krause, Anja Hoffmann‐Röder · Synthesis · 2001 · 942 citations

, , +9

Self‐Regeneration of Stereocenters (SRS)—Applications, Limitations, and Abandonment of a Synthetic Principle

Dieter Seebàch, Andrea Rolf Sting, Matthias Hoffmann · Angewandte Chemie International Edition in English · 1996 · 480 citations

, , +13

The asymmetric Michael addition reactions using chiral imines

Jean d’Angelo, Didier Desmaële, Françoise Dumas et al. · Tetrahedron Asymmetry · 1992 · 289 citations

, , +3

(α-Alkylation of α-heterosubstituted carboxylic acids without racemization

Dieter Seebàch, Reto Naef, Giorgio Calderari · Tetrahedron · 1984 · 285 citations

, , +3

Synthesis of a Muscarinic Receptor Antagonist via a Diastereoselective Michael Reaction, Selective Deoxyfluorination and Aromatic Metal−Halogen Exchange Reaction

Toshiaki Mase, Ioannis N. Houpis, Atsushi Akao et al. · The Journal of Organic Chemistry · 2001 · 92 citations