
TY  - JOUR
A1  - Ding, Yong 
A1  - Ma, Baochun 
A1  - Tong, Dejie 
A1  - Hua, Hui 
A1  - Zhao, Wei 
T1  - <i>Corrigendum to</i>: Synthesis of Epoxides Catalyzed by a Halide-Free Reaction-Controlled Phase-Transfer Catalytic System: [(CH<sub>3</sub>(CH<sub>2</sub>)<sub>17</sub>)<sub>2</sub>N(CH<sub>3</sub>)<sub>2</sub>]<sub>3</sub>[PW<sub>4</sub>O<sub>32</sub>]/H<sub>2</sub>O<sub>2</sub>/Dioxan/Olefin
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 2009
VL  - 62
IS  - 8
SP  - 947
EP  - 947
KW  - 
UR  - https://doi.org/10.1071/CH08547_CO 
N2  - The epoxidation of alkenes was successfully catalyzed by a recyclable catalytic system: [(CH3(CH2)17)2N(CH3)2]3[PW4O32]/H2O2/dioxan/olefin. This new catalytic system is not only capable of catalyzing homogeneous epoxidation of alkenes with a unique reaction-controlled phase-transfer character, but also avoids the use of chlorinated solvents. The reactions were conducted in a biphasic mixture of aqueous H2O2/dioxan, and many kinds of alkenes could be efficiently converted to the corresponding epoxides in high yields. Both new and used [(CH3(CH2)17)2N(CH3)2]3[PW4O32] catalyst was characterized by 31P magic angle spin NMR, and IR. 
ER  -

