Highly efficient oxidation of alcohols using Oxone® as oxidant catalyzed by ruthenium complex under mild reaction conditions

2008 ◽  
Vol 19 (9) ◽  
pp. 1031-1034 ◽  
Author(s):  
Zi Qiang Lei ◽  
Jian Qiang Wang ◽  
Peng Hua Yan
Synlett ◽  
2017 ◽  
Vol 28 (18) ◽  
pp. 2468-2472 ◽  
Author(s):  
Zheng Huang ◽  
Huaquan Fang ◽  
Qiaoxing He ◽  
Guixia Liu

Reported herein is a highly efficient intramolecular silylation of aromatic C–H bonds catalyzed by a pincer ruthenium complex, giving benzoxasiloles under relatively mild reaction conditions with broad substrate scope and low catalyst loadings. The silylation product can be further converted into a biaryl product by Pd-catalyzed Hiyama–­Denmark cross-coupling reactions.


2015 ◽  
Vol 51 (56) ◽  
pp. 11268-11271 ◽  
Author(s):  
Wen Dai ◽  
Ying Lv ◽  
Lianyue Wang ◽  
Sensen Shang ◽  
Bo Chen ◽  
...  

A novel strategy for catalytic oxidation of a variety of benzylic, allylic, propargylic, and aliphatic alcohols to the corresponding aldehydes or ketones has been successfully developed.


2010 ◽  
Vol 88 (9) ◽  
pp. 964-968 ◽  
Author(s):  
Zhaoqiong Jiang ◽  
Zhiqing Wu ◽  
Lixia Wang ◽  
Di Wu ◽  
Xiangge Zhou

A simple, highly efficient, and environmentally friendly protocol for the synthesis of primary aromatic amines by catalytic coupling of aromatic boronic acids with aqueous ammonia has been developed by using commercial and inexpensive CuSO4·5H2O as catalyst without addition of other solvents under mild reaction conditions.


2017 ◽  
Vol 41 (2) ◽  
pp. 88-92
Author(s):  
Shenggui Liu ◽  
Rongkai Pan ◽  
Wenyi Su ◽  
Guobi Li ◽  
Chunlin Ni

2,6-Bis[1-(pyridin-2-yl)-1H-benzo[d]-imidazol-2-yl]pyridine (bpbp), which has been synthesised by intramolecular thermocyclisation of N2,N6-bis[2-(pyridin-2-ylamino)phenyl]pyridine-2,6-dicarboxamide, reacts with sodium pyridine-2,6-dicarboxylate (pydic) and RuCl3 to give [Ru(bpbp)(pydic)] which can catalyse the oxidation of (1H-benzo[d]imidazol-2-yl)methanol to 1H-benzo[d]imidazole-2-carbaldehyde by H2O2. The optimal reaction conditions were: molar ratios of catalyst to substrate to H2O2 set at 1: 1000: 3000; reaction temperature 50 °C; reaction time 5 h. The yield of (1H-benzo[d]imidazol-2-yl) methanol was 70%.


ChemInform ◽  
2006 ◽  
Vol 37 (15) ◽  
Author(s):  
Qiao-xiang Kang ◽  
Ju-jie Luo ◽  
Yan-bin Bai ◽  
Zhi-wang Yang ◽  
Zi-qiang Lei

Author(s):  
Lin Gong ◽  
Ji Sun ◽  
Yousong Liu ◽  
Guangcheng Yang

The use of solar energy to drive efficient CO2 cycloaddition conversion under mild reaction conditions is highly desired but remains a significant challenge. In this communication, a Zn single-atoms-loaded N-doped...


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