RANEY® Ni catalyzed transfer hydrogenation of levulinate esters to γ-valerolactone at room temperature - Chemical Communications (RSC Publishing)
Effect of preparation conditions of Raney Nickel on its catalytic properties for slurry phase hydrogenation of o-nitrophenol to
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Selective Blockage Of The Catalyst Active Sites For The Hydrogenation Of Various Functional Groups Over Raney Nickel And Nickel Supported On Silica
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Molecules | Free Full-Text | Polymer-Supported Raney Nickel Catalysts for Sustainable Reduction Reactions
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Catalytic Transfer Hydrogenation of Glucose to Sorbitol with Raney Ni Catalysts Using Biomass-Derived Diols as Hydrogen Donors | ACS Sustainable Chemistry & Engineering
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Preparation and catalytic performance of an efficient Raney nickel catalyst for syngas methanation | SpringerLink
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The mechanism of Raney nickel action on the degradation of glycidyl-d5... | Download Scientific Diagram
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Molecules | Free Full-Text | Polymer-Supported Raney Nickel Catalysts for Sustainable Reduction Reactions
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A Two-Step Process for Conversion of Cellulose to γ-Valerolactone over Raney Ni Catalyst Using H2O as a Hydrogen Source | Earth, Space, and Environmental Chemistry | ChemRxiv | Cambridge Open Engage
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Molecules | Free Full-Text | Polymer-Supported Raney Nickel Catalysts for Sustainable Reduction Reactions
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Raney nickel coupled nascent hydrogen as a novel strategy for enhanced reduction of nitrate and nitrite - ScienceDirect
![What would be the major product of the following reaction sequence if step 6 were replaced by Raney Ni and H2. Additionally, what are the common name and pKa values of the What would be the major product of the following reaction sequence if step 6 were replaced by Raney Ni and H2. Additionally, what are the common name and pKa values of the](https://homework.study.com/cimages/multimages/16/55968976126252218480458996.png)