scholarly journals Effect of Metal Halides on the Selective Hydrogenation of Unsaturated Ketones with Raney Nickel.

1956 ◽  
Vol 59 (2) ◽  
pp. 236-239 ◽  
Author(s):  
Kazuo Hoshino ◽  
Ziro Miyata
1999 ◽  
Vol 29 (1) ◽  
pp. 129-134 ◽  
Author(s):  
Hui Wang ◽  
Hongzhen Lian ◽  
Jijun Chen ◽  
Yi Pan ◽  
Yaozeng Shi

2000 ◽  
Vol 154 (1-2) ◽  
pp. 237-241 ◽  
Author(s):  
Gabriella Fogassy ◽  
László Hegedűs ◽  
Antal Tungler ◽  
Albert Lévai ◽  
Tibor Máthé

1998 ◽  
Vol 171 (1) ◽  
pp. 117-122 ◽  
Author(s):  
Liu Baijun ◽  
Lu Lianhai ◽  
Wang Bingchun ◽  
Cai Tianxi ◽  
Katsuyoshi Iwatani

1983 ◽  
Vol 17 (1) ◽  
pp. 68-70
Author(s):  
A. I. Gontar' ◽  
O. S. Popov ◽  
É. M. Sul'man ◽  
T. V. Ankudinova ◽  
O. B. Sannikov ◽  
...  

1995 ◽  
Vol 73 (6) ◽  
pp. 846-852 ◽  
Author(s):  
Behzad Mahdavi ◽  
Philippe Chambrion ◽  
Julie Binette ◽  
Eric Martel ◽  
Jean Lessard

The selectivity of the electrocatalytic hydrogenation (ECH) of conjugated enones to the corresponding carbonyl compounds has been investigated in aqueous methanol under constant current at nickel boride, fractal nickel, and Raney nickel electrodes made of pressed powders. The influence of various parameters (water percentage, pH, concentration of substrate, and current density) on the selectivity of the carbon–carbon double bond hydrogenation was studied with cyclohex-2-en-1-one at nickel boride electrodes. Under given electrolysis conditions, fractal nickel electrodes were found to give the highest selectivity. The selectivity of the ECH of a variety of conjugated enones at fractal nickel electrodes was determined under electrolysis conditions that gave the best selectivity with cyclohexenone at nickel boride electrodes. Keywords: electrocatalytic hydrogenation, α,β-unsaturated ketones, selective hydrogenation, nickel based cathodes.


2016 ◽  
Vol 6 (20) ◽  
pp. 7386-7390 ◽  
Author(s):  
Wenjiang Li ◽  
Yanhua Wang ◽  
Pu Chen ◽  
Min Zeng ◽  
Jingyang Jiang ◽  
...  

Thermoregulated phase-transfer iridium nanoparticles exhibited a totally different hydrogenation orientation for α,β-unsaturated aldehydes and ketones.


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