Mechanism and Conditions for Highly Enantioselective Epoxidation of α,β-Enones Using Charge-Accelerated Catalysis by a Rigid Quaternary Ammonium Salt
- 18 September 1999
- journal article
- research article
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 1 (8) , 1287-1290
- https://doi.org/10.1021/ol990964z
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Enantioselective synthesis of β-hydroxy-α-amino acid esters by aldol coupling using a chiral quaternary ammonium salt as catalystTetrahedron Letters, 1999
- Highly Enantioselective Phase Transfer Catalyzed Alkylation of a 3-Oxygenated Propionic Ester Equivalent; Applications and MechanismJournal of the American Chemical Society, 1998
- A Rational Approach to Catalytic Enantioselective Enolate Alkylation Using a Structurally Rigidified and Defined Chiral Quaternary Ammonium Salt under Phase Transfer ConditionsJournal of the American Chemical Society, 1997
- Synthesis and Investigation of C2-Symmetric Optically Active Pyrrolidinium Salts as Chiral Phase-Transfer Catalysts.CHEMICAL & PHARMACEUTICAL BULLETIN, 1994
- The stereoselective synthesis of .alpha.-amino acids by phase-transfer catalysisJournal of the American Chemical Society, 1989
- Catalytic asymmetric induction in oxidation reactions. Synthesis of optically active epoxynaphthoquinonesThe Journal of Organic Chemistry, 1980
- Synthesis of optically active 2,3-epoxycyclohexanone and the determination of its absolute configurationThe Journal of Organic Chemistry, 1980
- Alkaloid assisted asymmetric synthesis IV additional routes to chiral epoxidesTetrahedron Letters, 1978
- Solvent effects in homogeneous asymmetric catalysisJournal of the Chemical Society, Chemical Communications, 1978
- Catalytic asymmetric induction in oxidation reactions. The synthesis of optically active epoxides.Tetrahedron Letters, 1976