1-(Pyridin-2-yl)methanamine-Based Ruthenium Catalysts for Fast Transfer Hydrogenation of Carbonyl Compounds in 2-Propanol

2008 ◽  
Vol 2008 (26) ◽  
pp. 4041-4053 ◽  
Author(s):  
Walter Baratta ◽  
Pierluigi Rigo
Keyword(s):  
Carbonyl Compounds ◽  
Ruthenium Catalysts ◽  
Transfer Hydrogenation

Highly efficient homogeneous and heterogenized ruthenium catalysts for transfer hydrogenation of carbonyl compounds

RSC Advances ◽  
2014 ◽  
Vol 4 (53) ◽  
pp. 27955-27962 ◽  
Author(s):  
S. Ganesamoorthy ◽  
P. Jerome ◽  
K. Shanmugasundaram ◽  
R. Karvembu
Keyword(s):  
Carbonyl Compounds ◽  
Ruthenium Catalysts ◽  
Transfer Hydrogenation ◽  
Highly Efficient

[Ru(acac)2(CH3CN)2] and its SiO2 immobilized form were found to be efficient catalysts for the transfer hydrogenation of carbonyl compounds.

Cyclometalated Dicarbonyl Ruthenium Catalysts for Transfer Hydrogenation and Hydrogenation of Carbonyl Compounds

2018 ◽  
Vol 37 (13) ◽  
pp. 2136-2146 ◽  
Author(s):  
Steven Giboulot ◽  
Salvatore Baldino ◽  
Maurizio Ballico ◽  
Hans Günter Nedden ◽  
Daniele Zuccaccia ◽  
...  
Keyword(s):  
Carbonyl Compounds ◽  
Ruthenium Catalysts ◽  
Transfer Hydrogenation

Recyclable Covalent Triazine Framework-based Ru Catalyst for Transfer Hydrogenation of Carbonyl Compounds in Water

2019 ◽  
Vol 7 (9) ◽  
pp. 8893-8899 ◽  
Author(s):  
Sudakar Padmanaban ◽  
Gunniya Hariyanandam Gunasekar ◽  
Mearae Lee ◽  
Sungho Yoon
Keyword(s):  
Carbonyl Compounds ◽  
Transfer Hydrogenation ◽  
Ru Catalyst ◽  
Covalent Triazine Framework

scholarly journals Catalytic Activity of High-Surface-Area Amorphous MgO Obtained from Upsalite

Catalysts ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 1338
Author(s):  
Marek Gliński ◽  
Ewa M. Iwanek (nee Wilczkowska) ◽  
Urszula Ulkowska ◽  
Agnieszka Czajka ◽  
Zbigniew Kaszkur
Keyword(s):  
Surface Area ◽  
Carbonyl Compounds ◽  
Main Product ◽  
High Surface ◽  
High Surface Area ◽  
Hydrogenation Reaction ◽  
Transfer Hydrogenation ◽  
Reaction Conditions ◽  
Synthesis Conditions ◽  
Transfer Hydrogenation Reaction

The first aim of the research was to synthesize a pure Upsalite, which is an amorphous form of MgCO3, by modifying a procedure described in the literature, so that it would be the precursor of a high-surface, amorphous magnesium oxide. The results indicate that within the studied reaction conditions, the type of alcohol used as the reactant has the most pronounced effect on the yield of reaction. From the two alcohols that led to the highest yield of Upsalite, methanol gave a substantially larger surface area (794 vs. 191 m2 g−1). The optimized synthesis conditions of Upsalite were used to obtain MgO via thermolysis, whose activity in the transfer hydrogenation reaction (THR) from ethanol, 2-propanol and 2-pentanol to various carbonyl compounds was determined. The optimal conditions for the thermolysis were as follows: vacuum, T = 673 K as the final temperature, and a heating rate of 2 deg min−1. The high-surface, amorphous magnesia (SBET = 488 m2 g−1) was found to be a very selective catalyst to 4-t-butylcyclohexanone in THR, which led to a diastereoselectivity of over 94% to the E-isomer of 4-t-butylcyclohexanol for more than 3 h, with conversions of up to 97% with either 2-propanol or 2-pentanol as the hydrogen donor. In the case of acrolein and 2-n-propylacrolein being used as the hydrogen acceptors, the unsaturated alcohol (UOL) was the main product of the reaction, with higher UOL yields noted for ethanol than 2-propanol.

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