Highly Efficient Epoxidation of Olefins Using Aqueous H2O2 and Catalytic Methyltrioxorhenium/Pyridine: Pyridine-Mediated Ligand Acceleration
- 1 July 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 119 (26), 6189-6190
- https://doi.org/10.1021/ja970623l
Abstract
No abstract availableThis publication has 20 references indexed in Scilit:
- A Practical Method for Epoxidation of Terminal Olefins with 30% Hydrogen Peroxide under Halide-Free ConditionsThe Journal of Organic Chemistry, 1996
- Pyridinium‐Ionen in Nachbarschaft zu Oxiranringen: nützliche Zwischenstufen zur stereospezifischen Synthese von β‐HydroxyketonenAngewandte Chemie, 1996
- Deactivation of Methylrhenium Trioxide−Peroxide Catalysts by Diverse and Competing PathwaysJournal of the American Chemical Society, 1996
- Kinetics and Mechanism of the Epoxidation of Alkyl-Substituted Alkenes by Hydrogen Peroxide, Catalyzed by Methylrhenium TrioxideThe Journal of Organic Chemistry, 1996
- Epoxidation of Styrenes by Hydrogen Peroxide As Catalyzed by Methylrhenium TrioxideJournal of the American Chemical Society, 1995
- Mechanistic study of the co-ordination of hydrogen peroxide to methylrhenium trioxideJ. Chem. Soc., Dalton Trans., 1995
- Methyltrioxorhenium as Catalyst of a Novel Aldehyde OlefinationAngewandte Chemie International Edition in English, 1991
- A new, effective catalytic system for epoxidation of olefins by hydrogen peroxide under phase-transfer conditionsThe Journal of Organic Chemistry, 1983
- m-Chloroperoxybenzoic acid-potassium fluoride system: study of its stability and reaction with .alpha.-methylstyreneThe Journal of Organic Chemistry, 1982
- Methyltrioxorhenium. An air-stable compound containing a carbon-rhenium bondInorganic Chemistry, 1979