Manganese‐Catalyzed Transfer Hydrogenation of Nitriles with 2‐Butanol as the Hydrogen Source

ChemCatChem ◽  
2019 ◽  
Vol 11 (21) ◽  
pp. 5330-5338 ◽  
Author(s):  
Jorge A. Garduño ◽  
Marcos Flores‐Alamo ◽  
Juventino J. García
Keyword(s):  
Transfer Hydrogenation ◽  
Hydrogenation Of Nitriles

Ruthenium-Catalyzed Transfer Hydrogenation of Nitriles: Reduction and SubsequentN-Monoalkylation to Secondary Amines

2013 ◽  
Vol 2013 (18) ◽  
pp. 3671-3674 ◽  
Author(s):  
Svenja Werkmeister ◽  
Christoph Bornschein ◽  
Kathrin Junge ◽  
Matthias Beller
Keyword(s):  
Transfer Hydrogenation ◽  
Secondary Amines ◽  
Hydrogenation Of Nitriles

Selective catalytic transfer hydrogenation of nitriles to primary amines using Pd/C

2014 ◽  
Vol 4 (3) ◽  
pp. 629 ◽  
Author(s):  
Marcelo Vilches-Herrera ◽  
Svenja Werkmeister ◽  
Kathrin Junge ◽  
Armin Börner ◽  
Matthias Beller
Keyword(s):  
Transfer Hydrogenation ◽  
Primary Amines ◽  
Catalytic Transfer Hydrogenation ◽  
Catalytic Transfer ◽  
Hydrogenation Of Nitriles

ChemInform Abstract: Ruthenium-Catalyzed Transfer Hydrogenation of Nitriles: Reduction and Subsequent N-Monoalkylation to Secondary Amines.

ChemInform ◽  
2013 ◽  
Vol 44 (45) ◽  
pp. no-no
Author(s):  
Svenja Werkmeister ◽  
Christoph Bornschein ◽  
Kathrin Junge ◽  
Matthias Beller
Keyword(s):  
Transfer Hydrogenation ◽  
Secondary Amines ◽  
Hydrogenation Of Nitriles

scholarly journals Cover Feature: Ru‐Catalyzed Transfer Hydrogenation of Nitriles, Aromatics, Olefins, Alkynes and Esters (ChemCatChem 21/2018)

ChemCatChem ◽  
2018 ◽  
Vol 10 (21) ◽  
pp. 4779-4779
Author(s):  
Iryna D. Alshakova ◽  
Bulat Gabidullin ◽  
Georgii I. Nikonov
Keyword(s):  
Transfer Hydrogenation ◽  
Hydrogenation Of Nitriles

Ru‐Catalyzed Transfer Hydrogenation of Nitriles, Aromatics, Olefins, Alkynes and Esters

ChemCatChem ◽  
2018 ◽  
Vol 10 (21) ◽  
pp. 4860-4869 ◽  
Author(s):  
Iryna D. Alshakova ◽  
Bulat Gabidullin ◽  
Georgii I. Nikonov
Keyword(s):  
Transfer Hydrogenation ◽  
Hydrogenation Of Nitriles

Multimetal-MOF-derived transition metal alloy NPs embedded in an N-doped carbon matrix: highly active catalysts for hydrogenation reactions

2016 ◽  
Vol 4 (26) ◽  
pp. 10254-10262 ◽  
Author(s):  
Jilan Long ◽  
Kui Shen ◽  
Liang Chen ◽  
Yingwei Li
Keyword(s):  
Transition Metal ◽  
Carbon Matrix ◽  
Catalytic Performance ◽  
Metal Alloy ◽  
Transfer Hydrogenation ◽  
Transition Metal Alloy ◽  
Highly Active ◽  
Hydrogenation Reactions ◽  
Excellent Catalytic Performance ◽  
Hydrogenation Of Nitriles

We report a MOF-templated route to synthesize transition metal alloy NPs embedded in an N-doped carbon matrix. The alloy-based catalysts exhibited excellent catalytic performance and widespread substrate applicability for the transfer hydrogenation of nitriles.

scholarly journals Tuning the selectivity of catalytic nitriles hydrogenation by structure regulation in atomically dispersed Pd catalysts

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Zhibo Liu ◽  
Fei Huang ◽  
Mi Peng ◽  
Yunlei Chen ◽  
Xiangbin Cai ◽  
...  
Keyword(s):  
Density Functional ◽  
Dissociative Adsorption ◽  
Transfer Hydrogenation ◽  
Secondary Amines ◽  
Primary Amines ◽  
Product Selectivity ◽  
Pd Catalysts ◽  
Catalytic Transfer ◽  
Pd Clusters ◽  
Hydrogenation Of Nitriles

AbstractThe product selectivity in catalytic hydrogenation of nitriles is strongly correlated with the structure of the catalyst. In this work, two types of atomically dispersed Pd species stabilized on the defect-rich nanodiamond-graphene (ND@G) hybrid support: single Pd atoms (Pd1/ND@G) and fully exposed Pd clusters with average three Pd atoms (Pdn/ND@G), were fabricated. The two catalysts show distinct difference in the catalytic transfer hydrogenation of nitriles. The Pd1/ND@G catalyst preferentially generates secondary amines (Turnover frequency (TOF@333 K 709 h−1, selectivity >98%), while the Pdn/ND@G catalyst exhibits high selectivity towards primary amines (TOF@313 K 543 h−1, selectivity >98%) under mild reaction conditions. Detailed characterizations and density functional theory (DFT) calculations show that the structure of atomically dispersed Pd catalysts governs the dissociative adsorption pattern of H2 and also the hydrogenation pathway of the benzylideneimine (BI) intermediate, resulting in different product selectivity over Pd1/ND@G and Pdn/ND@G, respectively. The structure-performance relationship established over atomically dispersed Pd catalysts provides valuable insights for designing catalysts with tunable selectivity.

Chemoselective transfer hydrogenation of nitriles to secondary amines with nickel(II) catalysts

2021 ◽  
Vol 511 ◽  
pp. 111738
Author(s):  
Vincent Vermaak ◽  
Hermanus C.M. Vosloo ◽  
Andrew J. Swarts
Keyword(s):  
Transfer Hydrogenation ◽  
Secondary Amines ◽  
Hydrogenation Of Nitriles
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