A Novel Methyltrioxorhenium (MTO)‐Catalyzed Epoxidation of Olefins: An Impressive Example of Simplicity, Selectivity, and Efficiency
- 15 December 1997
- journal article
- highlight
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 36 (23) , 2591-2592
- https://doi.org/10.1002/anie.199725911
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Alkylrhenium Oxides from Perrhenates: A New, Economical Access to Organometallic Oxide CatalystsAngewandte Chemie International Edition in English, 1997
- Alkylrheniumoxide aus Perrhenaten: ein neuer, ökonomischer Zugang zu Organometalloxid‐KatalysatorenAngewandte Chemie, 1997
- Highly Efficient Epoxidation of Olefins Using Aqueous H2O2 and Catalytic Methyltrioxorhenium/Pyridine: Pyridine-Mediated Ligand AccelerationJournal of the American Chemical Society, 1997
- Methyltrioxorhenium(VII)‐Catalyzed Epoxidation of Alkenes with the Urea/Hydrogen Peroxide AdductAngewandte Chemie International Edition in English, 1996
- Methyltrioxorhenium(VII)-katalysierte Epoxidierung von Alkenen mit Harnstoff-WasserstoffperoxidAngewandte Chemie, 1996
- Ligandenbeschleunigte KatalyseAngewandte Chemie, 1995
- Construction of Highly Efficient Mn-Salen Catalyst for Asymmetric Epoxidation of Conjugatedcis-OlefinsSynlett, 1994
- Methyltrioxorhenium(VII) als Epoxidationskatalysator: Struktur der aktiven Spezies und KatalysemechanismusAngewandte Chemie, 1993
- Methyltrioxorhenium as Catalyst for Olefin OxidationAngewandte Chemie International Edition in English, 1991
- Direct Epoxidation of Olefins Catalyzed by Nickel(II) Complexes with Molecular Oxygen and AldehydesBulletin of the Chemical Society of Japan, 1991