Ni Nanoparticles Stabilized by Poly(Ionic Liquids) as Chemoselective and Magnetically Recoverable Catalysts for Transfer Hydrogenation Reactions of Carbonyl Compounds

ChemCatChem ◽  
2016 ◽  
Vol 8 (6) ◽  
pp. 1139-1145 ◽  
Author(s):  
Kari Vijayakrishna ◽  
K. T. Prabhu Charan ◽  
Kasina Manojkumar ◽  
Sadhana Venkatesh ◽  
Nellepalli Pothanagandhi ◽  
...  
2021 ◽  
Author(s):  
Samanta Yadav ◽  
Paranthaman Vijayan ◽  
Sunil Yadav ◽  
Rajeev Gupta

Ru(ii) complexes of phosphine–amide ligands function as efficient catalysts for the transfer hydrogenation of assorted carbonyl compounds, including a few challenging biologically relevant substrates, using isopropanol as the hydrogen source.


2020 ◽  
Vol 73 (20-22) ◽  
pp. 2963-2977
Author(s):  
Sadhana Venkatesh ◽  
Rakesh R. Panicker ◽  
Verdhi Lenin Kumar ◽  
B. B. Pavankumar ◽  
Nukala Viswanath ◽  
...  

Catalysts ◽  
2019 ◽  
Vol 9 (6) ◽  
pp. 503 ◽  
Author(s):  
Masato Yoshida ◽  
Ryota Hirahata ◽  
Takayoshi Inoue ◽  
Takuya Shimbayashi ◽  
Ken-ichi Fujita

A new catalytic system for transfer hydrogenation of carbonyl compounds using glucose as a hydrogen donor was developed. Various ketones and aldehydes were efficiently converted to corresponding alcohols with two equivalents of glucose in the presence of a small amount (0.1 to 1.0 mol%) of iridium catalyst that had a functional ligand. In this catalytic system, transfer hydrogenation reactions proceeded based on the cooperativity of iridium and a functional ligand. It should be noted that environmentally benign water could have been used as a solvent in the present catalytic system for the reduction of various carbonyl substrates. Furthermore, the reaction scope could be extended by using N,N-dimethylacetamide as a reaction solvent.


RSC Advances ◽  
2013 ◽  
Vol 3 (4) ◽  
pp. 1050-1054 ◽  
Author(s):  
Manoj B. Gawande ◽  
Huizhang Guo ◽  
Anuj K. Rathi ◽  
Paula S. Branco ◽  
Yuanzhi Chen ◽  
...  

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