Copper-catalyzed oxidative cleavage of carbon–carbon double bond of enol ethers with molecular oxygen

2005 ◽  
Vol 690 (23) ◽  
pp. 5378-5382 ◽  
Author(s):  
Makoto Tokunaga ◽  
Yuki Shirogane ◽  
Hiroshi Aoyama ◽  
Yasushi Obora ◽  
Yasushi Tsuji
ChemInform ◽  
2006 ◽  
Vol 37 (11) ◽  
Author(s):  
Makoto Tokunaga ◽  
Yuki Shirogane ◽  
Hiroshi Aoyama ◽  
Yasushi Obora ◽  
Yasushi Tsuji

2012 ◽  
Vol 14 (16) ◽  
pp. 4158-4161 ◽  
Author(s):  
Riyuan Lin ◽  
Feng Chen ◽  
Ning Jiao

2019 ◽  
Vol 6 (6) ◽  
pp. 841-845 ◽  
Author(s):  
Zhen Cheng ◽  
Weiwei Jin ◽  
Chenjiang Liu

B2pin2-catalyzed oxidative cleavage of the CC double bond of an olefin with molecular oxygen as the oxidant and oxygen source has been developed.


2006 ◽  
Vol 10 (07) ◽  
pp. 942-947 ◽  
Author(s):  
Yong-Fei Li ◽  
Can-Cheng Guo ◽  
Xu-Hui Yan ◽  
Qiang Liu

The aerobic oxidative cleavage of styrene C=C double bonds catalyzed by simple manganese porphyrin is reported. Under the catalysis of chloro(tetraphenylporphinato)manganese, the oxidative cleavage of the carbon-carbon double bond of the styrene with air yields benzaldehyde. Our results show that the oxidative cleavage and the epoxidation of the styrene double bond are the competition reactions in the styrene-manganese porphyrin-air system. The reaction temperature decided the product distribution. Under the conditions of 0.4 MPa air and 30 ppm of chloro(tetraphenylporphinato)manganese, the styrene conversion was 20.0% and the selectivity of benzaldehyde and styrene oxide was 81.7% and 12.7% respectively when the reaction temperature was 110°C. Styrene conversion was 92.5% and the selectivity of benzaldehyde and styrene oxide was 48.1% and 41.2% respectively when the reaction temperature was 120°C.


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