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Semi-hydrogenation of alkynes using Ru/TPPTS as a biphasic recyclable catalyst in ethylene glycol-toluene solvent system

https://doi.org/10.1016/j.mcat.2018.09.008

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Aqueous‐Phase Organometallic Catalysis

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Highly Stereoselective Semihydrogenation of Alkynes Promoted by Nickel(0) Nanoparticles

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Efficient E‐Selective Transfer Semihydrogenation of Alkynes by Means of Ligand‐Metal Cooperating Ruthenium Catalyst

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Transfer Semihydrogenation of Alkynes Catalyzed by a Zero‐Valent Palladium N‐Heterocyclic Carbene Complex

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Catalytic Stereoselective Semihydrogenation of Alkynes to E‐Alkenes

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Stereodivergent Ruthenium‐Catalyzed Transfer Semihydrogenation of Diaryl Alkynes

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Aqueous‐Phase Organometallic Catalysis

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Ein neuer Katalysator für selektive Hydrierungen

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Ligand Assisted Rhodium Catalyzed Selective Semi‐hydrogenation of Alkynes Using Syngas and Molecular Hydrogen

inferredcites →https://doi.org/10.1016/0022-328x(95)05820-fopenalex-snapshot

Introducing TPPTS and related ligands for industrial biphasic processes

inferredcites →https://doi.org/10.1016/j.catcom.2013.04.015openalex-snapshot

Highly efficient and recyclable ruthenium nanoparticle catalyst for semihydrogenation of alkynes

inferredcites →https://doi.org/10.1016/j.cattod.2017.08.022openalex-snapshot

Reductive-hydroformylation of 1-octene to nonanol using fibrous Co 3 O 4 catalyst

inferredcites →https://doi.org/10.1016/j.jorganchem.2013.09.023openalex-snapshot

Nickel-catalyzed (E)-selective semihydrogenation of internal alkynes with hypophosphorous acid

inferredcites →https://doi.org/10.1016/j.mcat.2017.04.019openalex-snapshot

Highly regio-selective hydroformylation of biomass derived eugenol using aqueous biphasic Rh/TPPTS/CDs as a greener and recyclable catalyst

inferredcites →https://doi.org/10.1016/j.molcata.2016.01.004openalex-snapshot

Silica supported palladium phosphine as a robust and recyclable catalyst for semi-hydrogenation of alkynes using syngas

inferredcites →https://doi.org/10.1016/s0020-1693(00)88906-9openalex-snapshot

Homogeneous hydrogenations in aqueous solution catalyzed by ruthenium-phospine complexes

inferredcites →https://doi.org/10.1016/s0040-4039(98)02225-4openalex-snapshot

Comparison of activity and selectivity of various metal-TPPTS complex catalysts in ethylene glycol toluene biphasic Heck vinylation reactions of iodobenzene

inferredcites →https://doi.org/10.1016/s1381-1169(01)00150-9openalex-snapshot

Hydrogenation of carbon–carbon multiple bonds: chemo-, regio- and stereo-selectivity

inferredcites →https://doi.org/10.1021/acs.orglett.6b03254openalex-snapshot

E - and Z -Selective Transfer Semihydrogenation of Alkynes Catalyzed by Standard Ruthenium Olefin Metathesis Catalysts

inferredcites →https://doi.org/10.1021/acscatal.6b03140openalex-snapshot

Selective Semihydrogenation of Alkynes with N-Graphitic-Modified Cobalt Nanoparticles Supported on Silica

inferredcites →https://doi.org/10.1021/acscatal.6b03441openalex-snapshot

Gold–Ligand-Catalyzed Selective Hydrogenation of Alkynes into cis-Alkenes via H2 Heterolytic Activation by Frustrated Lewis Pairs

inferredcites →https://doi.org/10.1021/acscatal.7b02915openalex-snapshot

Highly Selective Semihydrogenation of Alkynes to Alkenes by Using an Unsupported Nanoporous Palladium Catalyst: No Leaching of Palladium into the Reaction Mixture

inferredcites →https://doi.org/10.1021/cr00039a008openalex-snapshot

Asymmetric Hydroformylation

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Chemical Routes for the Transformation of Biomass into Chemicals

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Are Alkyne Reductions Chemo-, Regio-, and Stereoselective Enough To Provide Pure ( Z )-Olefins in Polyfunctionalized Bioactive Molecules?

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Chemicals from Alkynes with Palladium Catalysts

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Photoalignment of Liquid-Crystal Systems

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Efficient Catalytic System for Synthesis of trans-Stilbene from Diphenylacetylene Using Rh-Based Intermetallic Compounds

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Kinetic and Spectroscopic Studies of the [Palladium(Ar-bian)]-Catalyzed Semi-Hydrogenation of 4-Octyne

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Gold Nanocluster-Catalyzed Semihydrogenation: A Unique Activation Pathway for Terminal Alkynes

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Industrial Aqueous Biphasic Catalysis: Status and Directions

inferredcites →https://doi.org/10.1038/373501a0openalex-snapshot

Enhancement of interfacial catalysis in a biphasic system using catalyst-binding ligands

inferredcites →https://doi.org/10.1039/c6cc09067bopenalex-snapshot

Copper( i )-catalysed transfer hydrogenations with ammonia borane

inferredcites →https://doi.org/10.1039/c7cc01228dopenalex-snapshot

Cobalt-catalyzed (Z)-selective semihydrogenation of alkynes with molecular hydrogen

inferredcites →https://doi.org/10.1055/s-0034-1379896openalex-snapshot

Copper-Catalyzed Semihydrogenation of Alkynes to Z-Alkenes

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Catalytic Hydrogenation of Naturally Occurring Allylbenzenes by the Water-Soluble Complex Ru(H)2(Co)(O-Tppts)3 in Aqueous Biphasic System

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Ruthenium‐Catalyzed E‐Selective Partial Hydrogenation of Alkynes under Transfer‐Hydrogenation Conditions using Paraformaldehyde as Hydrogen Source

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Synthesis of Leaf Alcohol Using Lindlar Catalyst: From Batch to Continuous‐Flow

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Preparation of semi-hydrogenation catalysts by embedding Pd in layered double hydroxides nanocages via sacrificial template of ZIF-67

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Aqueous-biphasic catalysis: A technological alternative for the use of organometallic complexes in hydrogenation and hydroformylation reactions with possible industrial application

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A combined catalytic and kinetic study of the aqueous-biphasic hydrogenation of allylbenzenes by using a dihydride-ruthenium complex containing tri(sodium-o-sulfonatedphenylphosphine) ligands

inferred← citeshttps://doi.org/10.1016/j.mcat.2020.111081openalex-snapshot

Design of hypercrosslinked poly(ionic liquid)s for efficiently catalyzing high-selective hydrogenation of phenylacetylene under ambient conditions

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Fabrication and first-principles calculations of aminoclay-derived nickel nanoparticles for selective semi-hydrogenation of alkynes: The impact of aminopropyl groups

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Intermetallic Pd In /Al2O3 catalysts with isolated single-atom Pd sites for one-pot hydrogenation of diphenylacetylene into trans-stilbene

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Renaissance in Alkyne Semihydrogenation: Mechanism, Selectivity, Functional Group Tolerance, and Applications in Organic Synthesis

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Quadrol-Pd( ii ) complexes: phosphine-free precatalysts for the room-temperature Suzuki–Miyaura synthesis of nucleoside analogues in aqueous media

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Green innovations in C–H bond functionalisation: exploring homogeneous recyclable catalytic systems

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A Review on Chemical Synthesis of Leaf Alcohol

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