Ruthenium Porphyrin-Catalyzed Aerobic Oxidation of Terminal Aryl Alkenes to Aldehydes by a Tandem Epoxidation-Isomerization Pathway

2008 ◽  
Vol 120 (35) ◽  
pp. 6740-6744 ◽  
Author(s):  
Gaoxi Jiang ◽  
Jian Chen ◽  
Hung-Yat Thu ◽  
Jie-Sheng Huang ◽  
Nianyong Zhu ◽  
...  
2008 ◽  
Vol 47 (35) ◽  
pp. 6638-6642 ◽  
Author(s):  
Gaoxi Jiang ◽  
Jian Chen ◽  
Hung-Yat Thu ◽  
Jie-Sheng Huang ◽  
Nianyong Zhu ◽  
...  

ChemInform ◽  
2008 ◽  
Vol 39 (50) ◽  
Author(s):  
Gaoxi Jiang ◽  
Jian Chen ◽  
Hung-Yat Thu ◽  
Jie-Sheng Huang ◽  
Nianyong Zhu ◽  
...  

2019 ◽  
Vol 9 (3) ◽  
pp. 811-821 ◽  
Author(s):  
Zhao-Meng Wang ◽  
Li-Juan Liu ◽  
Bo Xiang ◽  
Yue Wang ◽  
Ya-Jing Lyu ◽  
...  

The catalytic activity decreases as –(SiO)3Mo(OH)(O) > –(SiO)2Mo(O)2 > –(O)4–MoO.


2018 ◽  
Author(s):  
Asim Maity ◽  
Sung-Min Hyun ◽  
Alan Wortman ◽  
David Powers

<p>Hypervalent iodine(V) reagents, such as Dess-Martin periodinane (DMP) and 2-iodoxybenzoic acid (IBX), are broadly useful oxidants in chemical synthesis. Development of strategies to access these reagents from O2 would immediately enable use of O2 as a terminal oxidant in a broad array of substrate oxidation reactions. Recently we disclosed the aerobic synthesis of I(III) reagents by intercepting reactive oxidants generated during aldehyde autoxidation. Here, we couple aerobic oxidation of iodobenzenes with disproportionation of the initially generated I(III) compounds to generate I(V) reagents. The aerobically generated I(V) reagents exhibit substrate oxidation chemistry analogous to that of DMP. Further, the developed aerobic generation of I(V) has enabled the first application of I(V) intermediates in aerobic oxidation catalysis.</p>


2012 ◽  
Vol 9 (3) ◽  
pp. 319-340
Author(s):  
Bo-Tao Xin ◽  
Qing-Fa Zhou ◽  
Tao Lu
Keyword(s):  

2018 ◽  
Vol 8 (23) ◽  
pp. 6173-6179 ◽  
Author(s):  
Xu Jin ◽  
Rengui Li ◽  
Yue Zhao ◽  
Xiaodan Liu ◽  
Xiaoqi Wang ◽  
...  

Efficient converting of alcohols to aldehydes under visible light can be achieved on BiVO4 crystals with spatial separation of dual-cocatalysts.


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