ChemInform Abstract: Transfer Hydrogenation of Nitroarenes into Anilines by Palladium Nanoparticles via Dehydrogenation of Dimethylamine Borane Complex.

ChemInform ◽  
2016 ◽  
Vol 47 (10) ◽  
pp. no-no
Author(s):  
Nilesh M. Patil ◽  
Manohar A. Bhosale ◽  
Bhalchandra M. Bhanage
Keyword(s):  
Palladium Nanoparticles ◽  
Transfer Hydrogenation ◽  
Dimethylamine Borane

Transfer hydrogenation of nitroarenes into anilines by palladium nanoparticles via dehydrogenation of dimethylamine borane complex

RSC Advances ◽  
2015 ◽  
Vol 5 (105) ◽  
pp. 86529-86535 ◽  
Author(s):  
Nilesh M. Patil ◽  
Manohar A. Bhosale ◽  
Bhalchandra M. Bhanage
Keyword(s):  
Catalytic System ◽  
Palladium Nanoparticles ◽  
Reducing Agent ◽  
Water Soluble ◽  
Transfer Hydrogenation ◽  
Dimethylamine Borane

Reduction of nitroarenes to corresponding amines ​via dehydrogenation of dimethylamine borane using Pd NPs as a catalyst. The developed catalytic system uses dimethylamine borane as a reducing agent which is highly stable, water soluble and non-toxic.

Immobilized ruthenium metal-containing ionic liquid-catalyzed dehydrogenation of dimethylamine borane complex for the reduction of olefins and nitroarenes

RSC Advances ◽  
2016 ◽  
Vol 6 (57) ◽  
pp. 52347-52352 ◽  
Author(s):  
Nilesh M. Patil ◽  
Takehiko Sasaki ◽  
Bhalchandra M. Bhanage
Keyword(s):  
Ionic Liquid ◽  
Reducing Agent ◽  
Transfer Hydrogenation ◽  
Dimethylamine Borane

An efficient immobilized ruthenium metal containing ionic liquid (ImmRu-IL) catalyst has been developed for the transfer hydrogenation of olefins and nitroarenes. This methodology uses eco-friendly dimethylamine borane as a reducing agent.

Ruthenium-catalysed transfer hydrogenation reactions with dimethylamine borane

2011 ◽  
Vol 52 (49) ◽  
pp. 6652-6654 ◽  
Author(s):  
Tracy D. Nixon ◽  
Michael K. Whittlesey ◽  
Jonathan M.J. Williams
Keyword(s):  
Transfer Hydrogenation ◽  
Dimethylamine Borane ◽  
Hydrogenation Reactions

An efficient ligand free chemoselective transfer hydrogenation of olefinic bonds by palladium nanoparticles in an aqueous reaction medium

RSC Advances ◽  
2014 ◽  
Vol 4 (62) ◽  
pp. 32834-32839 ◽  
Author(s):  
Dattatraya B. Bagal ◽  
Bhalchandra M. Bhanage
Keyword(s):  
Catalytic System ◽  
Palladium Nanoparticles ◽  
Reaction Medium ◽  
Transfer Hydrogenation ◽  
Effective Catalyst ◽  
Ligand Free ◽  
Unsaturated Carbonyls

An efficient ligand free catalytic system was developed for chemoselective 1,4-reduction of various α,β-unsaturated carbonyls by palladium nanoparticles in aqueous reaction medium with excellent chemoselectivity and effective catalyst recyclability.

Palladium nanoparticles supported on nanosheet-like graphitic carbon nitride for catalytic transfer hydrogenation reaction

2020 ◽  
Vol 10 (23) ◽  
pp. 7883-7893
Author(s):  
Yan-Jhu Chou ◽  
Hao-Chuan Ku ◽  
Cheng-Chi Chien ◽  
Chechia Hu ◽  
Wen-Yueh Yu
Keyword(s):  
Palladium Nanoparticles ◽  
Carbon Nitride ◽  
Pd Nanoparticles ◽  
Hydrogenation Reaction ◽  
Transfer Hydrogenation ◽  
Catalytic Transfer Hydrogenation ◽  
Ambient Conditions ◽  
Catalytic Transfer ◽  
Transfer Hydrogenation Reaction ◽  
Pyridinic N

Pd/g-C3N4 catalysts with well-dispersed, electron-enriched Pd nanoparticles immobilized on pyridinic N atoms of g-C3N4 are active for catalytic transfer hydrogenation under ambient conditions.

Highly dispersed ultrafine palladium nanoparticles encapsulated in a triazinyl functionalized porous organic polymer as a highly efficient catalyst for transfer hydrogenation of aldehydes

2018 ◽  
Vol 6 (37) ◽  
pp. 18242-18251 ◽  
Author(s):  
Jin Yang ◽  
Man Yuan ◽  
Dan Xu ◽  
Hong Zhao ◽  
Yangyang Zhu ◽  
...  
Keyword(s):  
Palladium Nanoparticles ◽  
Catalytic Reduction ◽  
Aromatic Aldehydes ◽  
Transfer Hydrogenation ◽  
Organic Polymer ◽  
Efficient Catalyst ◽  
Porous Organic Polymer ◽  
Mild Conditions ◽  
Highly Dispersed ◽  
Organic Pores

A stable Pd@TP-POP catalyst with highly dispersed ultrafine Pd NPs confined in its organic pores was fabricated for catalytic reduction of 4-nitrophenol and transfer hydrogenation of aromatic aldehydes under very mild conditions.

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