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Raney Ni as Recyclable and Selective Catalyst for the Reduction of α‐Pinene to cis ‐Pinane with NaBH 4 at Room Temperature
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.201407723openalex-snapshot
A Palladium Nanoparticle–Nanomicelle Combination for the Stereoselective Semihydrogenation of Alkynes in Water at Room Temperature
inferredcites →https://doi.org/10.1002/cber.19931261016openalex-snapshot
Chemoselectivity in Catalytic Transfer Hydrogenation — Reduction of Alkenes and Alkynes with the H2PO2—NH4+ · H2O/Pd‐C System
inferredcites →https://doi.org/10.1002/cctc.201802044openalex-snapshot
Mild Hydrogenation of α‐Pinene Catalyzed by Ru Nanoparticles Loaded on Boron‐doped Amphiphilic Core‐Shell Mesoporous Molecular Sieves
inferredcites →https://doi.org/10.1007/s11172-008-0279-1openalex-snapshot
Catalytic activity of the VIII Group metals in the hydrogenation and isomerization of α- and β-pinenes
inferredcites →https://doi.org/10.1007/s11814-017-0307-7openalex-snapshot
Process optimization for selective hydrogenation of α-pinene over Ni/AlPO4
inferredcites →https://doi.org/10.1016/j.apcatb.2014.10.035openalex-snapshot
Water: the most effective solvent for liquid-phase hydrodechlorination of chlorophenols over Raney Ni catalyst
inferredcites →https://doi.org/10.1016/j.crci.2018.09.002openalex-snapshot
Highly selective solvent-free hydrogenation of pinenes to added-value cis-pinane
inferredcites →https://doi.org/10.1016/j.jiec.2014.12.005openalex-snapshot
A recyclable Pd colloidal catalyst for liquid phase hydrogenation of α-pinene
inferredcites →https://doi.org/10.1016/j.mcat.2017.10.020openalex-snapshot
Highly selective hydrogenation of α-pinene in aqueous medium using PVA-stabilized Ru nanoparticles
inferredcites →https://doi.org/10.1016/j.molcata.2007.05.020openalex-snapshot
Rapid, efficient and selective reduction of aromatic nitro compounds with sodium borohydride and Raney nickel
inferredcites →https://doi.org/10.1016/j.molcata.2016.09.007openalex-snapshot
Magnetically recyclable Ru immobilized on amine-functionalized magnetite nanoparticles and its high selectivity to prepare cis -pinane
inferredcites →https://doi.org/10.1016/j.tet.2007.01.053openalex-snapshot
Scope, limitations and mechanistic aspects in the selective homogeneous palladium-catalyzed reduction of alkenes under transfer hydrogen conditions
inferredcites →https://doi.org/10.1016/j.tetlet.2007.10.017openalex-snapshot
Selective reduction of mono- and disubstituted olefins by NaBH4 and catalytic RuCl3
inferredcites →https://doi.org/10.1016/j.tetlet.2009.11.061openalex-snapshot
A convenient methodology for the chemoselective reduction of a wide variety of functionalized alkenes
inferredcites →https://doi.org/10.1016/s0040-4039(01)81215-6openalex-snapshot
Hydroboration or hydrogenation of alkenes with CoCl2-NaBH4
inferredcites →https://doi.org/10.1021/acs.iecr.7b02523openalex-snapshot
Intrinsic Kinetics of Three-Phase Slurry Hydrogenation of o-Nitrocardanol to o-Aminocardanol over Raney Nickel Catalyst
inferredcites →https://doi.org/10.1021/jo01320a033openalex-snapshot
Selective reduction of mono- and disubstituted olefins by sodium borohydride and cobalt(II)
inferredcites →https://doi.org/10.1039/b505873bopenalex-snapshot
Biphasic hydrogenation of α-pinene in high-pressure carbon dioxide
inferredcites →https://doi.org/10.1039/c4ob00945bopenalex-snapshot
Iron-catalysed, general and operationally simple formal hydrogenation using Fe(OTf) 3 and NaBH 4
inferredcites →https://doi.org/10.1039/c7cc02140bopenalex-snapshot
Ligand-free nickel-catalyzed semihydrogenation of alkynes with sodium borohydride: a highly efficient and selective process for cis-alkenes under ambient conditions
inferredcites →https://doi.org/10.1039/c8ra00905hopenalex-snapshot
Sodium borohydride-nickel chloride hexahydrate in EtOH/PEG-400 as an efficient and recyclable catalytic system for the reduction of alkenes
inferredcites →https://doi.org/10.1039/c9ra00675copenalex-snapshot
The conversion of α-pinene to cis -pinane using a nickel catalyst supported on a discarded fluid catalytic cracking catalyst with an ionic liquid layer
inferredcites →https://doi.org/10.1080/00397911.2010.533239openalex-snapshot
Raney Nickel–Catalyzed Hydrogenation of Unsaturated Carboxylic Acids with Sodium Borohydride in Water
inferredcites →https://doi.org/10.1080/00397911.2011.562063openalex-snapshot
Convenient Method for Reduction of C-N Double Bonds in Oximes, Imines, and Hydrazones Using Sodium Borohydride–Raney Ni System
inferredcites →https://doi.org/10.1080/00397911.2018.1560875openalex-snapshot
Efficient and selective reduction of α-pinene to cis-pinane by NaBH4 using NiCl2•6H2O/PEG-800/ethanol as the catalytic system
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Efficient hydrogenation of rosin and α-pinene catalyzed by amphiphilic Ni–W–B catalysts
inferred← citeshttps://doi.org/10.1016/j.indcrop.2022.115140openalex-snapshot
Aqueous-phase hydrogenation of α-pinene catalyzed by Ni-B alloys loaded on a Janus amphiphilic carbon@silica nanomaterial
inferred← citeshttps://doi.org/10.1016/j.inoche.2025.115430openalex-snapshot
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Aqueous Hydrogenation of Rosin Catalyzed by Amphiphilic Ni–Cu Nanocatalysts
inferred← citeshttps://doi.org/10.1038/s41598-025-13119-8openalex-snapshot
Lignocellulosic biomass based catalysis for hydrogen generation effect of pistachio shells and Raney nickel in NaBH4 hydrolysis
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