Synthesis and catalytic properties in olefin epoxidation of chiral oxazoline dioxomolybdenum(VI) complexes

Keyphrases

• Catalytic Properties 100%
• Olefin Epoxidation 100%
• Chloro Complexes 100%
• Dioxomolybdenum(VI) 100%
• Chiral Oxazoline 100%
• Epoxides 66%
• Diols 66%
• α-methylstyrene 66%
• Enantiomeric Excess 66%
• 1H nuclear Magnetic Resonance (1H NMR) 33%
• Elemental Analysis 33%
• 29Si NMR 33%
• Bidentate 33%
• Benzyl 33%
• Dichloromethane 33%
• Reaction Time 33%
• Catalytic Activity 33%
• 2-oxazoline 33%
• Thermogravimetric Analysis 33%
• Epoxidation 33%
• Support Material 33%
• MAS NMR Spectroscopy 33%
• Asymmetric Induction 33%
• MCM-41 33%
• Oxazoline Ligands 33%
• Catalytic Epoxidation 33%
• Ordered Mesoporous Silica 33%
• Cumene Hydroperoxide 33%
• MoO2 33%
• IR Spectroscopy Analysis 33%
• Mesoporous MCM-41 33%
• Cyclooctene Epoxidation 33%
• MoO2Cl2 33%
• Tert-butyl Hydroperoxide (t-BHP) 33%
• Catalytic Asymmetric 33%
• Grafted Catalyst 33%

Chemistry

• Alkene 100%
• Oxazoline 100%
• Catalyst Property 100%
• epoxidation 100%
• Epoxide 66%
• Enantiomer 66%
• Diol 66%
• 1H NMR Spectroscopy 33%
• Elemental Analysis 33%
• Thermogravimetric Analysis 33%
• MAS NMR Spectroscopy 33%
• Ordered Mesoporous Silica 33%
• Dichloromethane 33%
• 29Si MAS NMR 33%
• Cumene Hydroperoxide 33%
• Catalyst Activity 33%
• IR spectroscopy 33%

Chemical Engineering

• Olefin 100%
• Dichloromethane 100%
• Chemical Element 100%