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Bulky monophosphite ligands for ethene hydroformylation

https://doi.org/10.1016/j.jcat.2012.11.031
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Erste effiziente Hydroaminomethylierung mit Ammoniak: mit dualen Metallkatalysatoren und Zweiphasenkatalyse zu primären Aminen
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Assembly of Encapsulated Transition Metal Catalysts
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Homogeneous Catalysts
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Formation of Acetals under Rhodium‐Catalyzed Hydroformylation Conditions in Alcohols
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Supramolecular Catalyst for Aldehyde Hydrogenation and Tandem Hydroformylation–Hydrogenation
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Cover Picture: The Nature of the Extraordinary Finish of Stradivari’s Instruments (Angew. Chem. Int. Ed. 1/2010)
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Continuous Rhodium‐Catalyzed Hydroformylation of 1‐Octene with Polyhedral Oligomeric Silsesquioxanes (POSS) Enlarged Triphenylphosphine
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Supramolecular Control of Ligand Coordination and Implications in Hydroformylation Reactions
inferredcites →https://doi.org/10.1002/cctc.200900088openalex-snapshot
Fast and Selective Hydroaminomethylation Using Xanthene‐Based Amino‐Functionalized Ligands
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Rhodium‐Catalyzed Hydroformylation Using Hindered Phosphine Ligands: An In Situ Study
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The Rate‐Determining Step in the Rhodium–Xantphos‐Catalysed Hydroformylation of 1‐Octene
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Bioinspired Catalyst Design and Artificial Metalloenzymes
inferredcites →https://doi.org/10.1007/0-306-46947-2_4openalex-snapshot
Phosphines as ligands
inferredcites →https://doi.org/10.1007/0-306-46947-2_8openalex-snapshot
Process aspects of rhodium-catalyzed hydroformylation
inferredcites →https://doi.org/10.1007/1-4020-4087-3openalex-snapshot
Catalyst Separation, Recovery and Recycling
inferredcites →https://doi.org/10.1016/0022-328x(95)05748-eopenalex-snapshot
Rhodium-catalysed hydroformylation of branched 1-alkenes; bulky phosphite vs. triphenylphosphine as modifying ligand
inferredcites →https://doi.org/10.1016/0304-5102(90)85016-bopenalex-snapshot
Copolymerization of ethylene and carbon monoxide by rhodium carbonyls
inferredcites →https://doi.org/10.1016/1381-1169(95)00130-1openalex-snapshot
Progress in hydroformylation and carbonylation
inferredcites →https://doi.org/10.1016/j.catcom.2011.05.001openalex-snapshot
Reactive separation of dilute ethylene by hydroformylation using slurried rhodium catalysts on phosphinated resins and silica
inferredcites →https://doi.org/10.1016/j.fluid.2005.02.010openalex-snapshot
The experiments and correlations of the solubility of ethylene in toluene solvent
inferredcites →https://doi.org/10.1016/j.jorganchem.2005.02.026openalex-snapshot
Supraphos: A supramolecular strategy to prepare bidentate ligands
inferredcites →https://doi.org/10.1016/s0022-328x(00)99279-9openalex-snapshot
Hydroformylation of less reactive olefins with modified rhodium catalysts
inferredcites →https://doi.org/10.1016/s0040-4020(02)00211-9openalex-snapshot
Hydroformylation of higher olefins by rhodium/tris-((1H,1H,2H,2H-perfluorodecyl)phenyl)phosphites complexes in a fluorocarbon/hydrocarbon biphasic medium: effects of fluorinated groups on the activity and stability of the catalytic system
inferredcites →https://doi.org/10.1016/s1351-4180(11)70444-5openalex-snapshot
Homogeneous Catalysts: Activity – Stability – Deactivation
inferredcites →https://doi.org/10.1021/ar7001039openalex-snapshot
Ligands for Practical Rhodium-Catalyzed Asymmetric Hydroformylation
inferredcites →https://doi.org/10.1021/cr00039a008openalex-snapshot
Asymmetric Hydroformylation
inferredcites →https://doi.org/10.1021/cr1002497openalex-snapshot
Phosphite-Containing Ligands for Asymmetric Catalysis
inferredcites →https://doi.org/10.1021/cr970413ropenalex-snapshot
Tandem Reaction Sequences under Hydroformylation Conditions: New Synthetic Applications of Transition Metal Catalysis
inferredcites →https://doi.org/10.1021/i360056a007openalex-snapshot
Hydroformylation with Cobalt Carbonyl and Cobalt Carbonyl-Tributylphosphine Catalysts
inferredcites →https://doi.org/10.1021/ic701547hopenalex-snapshot
Quantitative Assessment of the Stereoelectronic Profile of Phosphine Ligands
inferredcites →https://doi.org/10.1021/ie0509701openalex-snapshot
Asymmetric Hydroformylation of Styrene in Supercritical Carbon Dioxide
inferredcites →https://doi.org/10.1021/ie970497uopenalex-snapshot
Kinetics of Hydroformylation of Ethylene in a Homogeneous Medium: Comparison in Organic and Aqueous Systems
inferredcites →https://doi.org/10.1021/ja029499iopenalex-snapshot
The Rh4(CO)12-Catalyzed Hydroformylation of 3,3-Dimethylbut-1-ene Promoted with HMn(CO)5. Bimetallic Catalytic Binuclear Elimination as an Origin for Synergism in Homogeneous Catalysis
inferredcites →https://doi.org/10.1021/ja030143wopenalex-snapshot
Amines Made Easily: A Highly Selective Hydroaminomethylation of Olefins
inferredcites →https://doi.org/10.1021/ja106674nopenalex-snapshot
Enantioselective Hydroformylation of N-Vinyl Carboxamides, Allyl Carbamates, and Allyl Ethers Using Chiral Diazaphospholane Ligands
inferredcites →https://doi.org/10.1021/ja208589copenalex-snapshot
“Cofactor”-Controlled Enantioselective Catalysis
inferredcites →https://doi.org/10.1021/ja9738337openalex-snapshot
Molecular Engineering in Homogeneous Catalysis: One-Phase Catalysis Coupled with Biphase Catalyst Separation. The Fluorous-Soluble HRh(CO){P[CH2CH2(CF2)5CF3]3}3 Hydroformylation System
inferredcites →https://doi.org/10.1021/ja980729wopenalex-snapshot
Rhodium-Catalyzed Hydroformylation in Supercritical Carbon Dioxide
inferredcites →https://doi.org/10.1021/ol801247vopenalex-snapshot
Highly Regioselective Isomerization−Hydroformylation of Internal Olefins to Linear Aldehyde Using Rh Complexes with Tetraphosphorus Ligands
inferredcites →https://doi.org/10.1021/om00001a010openalex-snapshot
Hydroformylation with a Rhodium/Bulky Phosphite Modified Catalyst. A Comparison of the Catalyst Behavior for Oct-1-ene, Cyclohexene, and Styrene
inferredcites →https://doi.org/10.1021/om00006a057openalex-snapshot
New Diphosphine Ligands Based on Heterocyclic Aromatics Inducing Very High Regioselectivity in Rhodium-Catalyzed Hydroformylation: Effect of the Bite Angle
inferredcites →https://doi.org/10.1021/om020854nopenalex-snapshot
Rhodium-Catalyzed Hydroformylation of Alkenes Using in Situ High-Pressure IR and Polymer Matrix Techniques
inferredcites →https://doi.org/10.1021/om030202eopenalex-snapshot
Homogeneous Hydroformylation of Ethylene Catalyzed by Rh4(CO)12. The Application of BTEM to Identify a New Class of Rhodium Carbonyl Spectra: RCORh(CO)3(π-C2H4)
inferredcites →https://doi.org/10.1021/om100250ropenalex-snapshot
Isostructural Phosphine−Phosphite Ligands in Rhodium-Catalyzed Asymmetric Hydroformylation
inferredcites →https://doi.org/10.1021/om2000508openalex-snapshot
A New Diphosphite Promoting Highly Regioselective Rhodium-Catalyzed Hydroformylation
inferredcites →https://doi.org/10.1021/om980531kopenalex-snapshot
The Unmodified Homogeneous Rhodium-Catalyzed Hydroformylation of Cyclohexene and the Search for Monometallic Catalytic Binuclear Elimination
inferredcites →https://doi.org/10.1021/om990523jopenalex-snapshot
New Phosphacyclic Diphosphines for Rhodium-Catalyzed Hydroformylation
inferredcites →https://doi.org/10.1021/om990734oopenalex-snapshot
Origin of the Bite Angle Effect on Rhodium Diphosphine Catalyzed Hydroformylation
inferredcites →https://doi.org/10.1039/b416917dopenalex-snapshot
Rhodium hydride formation in the presence of a bulky monophosphite ligand: a spectroscopic and solid-state investigation
inferredcites →https://doi.org/10.1039/b616186copenalex-snapshot
Supported ionic liquid phase catalysis with supercritical flow
inferredcites →https://doi.org/10.1039/b913778eopenalex-snapshot
Rational design of diphosphorus ligands – a route to superior catalysts
inferredcites →https://doi.org/10.1039/c2cy00450jopenalex-snapshot
“On-water” rhodium-catalysed hydroformylation for the production of linear alcohols
inferredcites →https://doi.org/10.1039/c39910001096openalex-snapshot
Hydroformylation of oct-1-ene with extremely high rates using rhodium catalysts containing bulky phosphites
inferredcites →https://doi.org/10.1039/dt9960001161openalex-snapshot
Direct formation of alcohols by hydrocarbonylation of alkenes under mild conditions using rhodium trialkylphosphine catalysts
inferredcites →https://doi.org/10.1039/p29870001597openalex-snapshot
Structural characterisation in solution of intermediates in rhodium-catalysed hydroformylation and their interconversion pathways
inferredcites →https://doi.org/10.1111/j.1749-6632.1974.tb25314.xopenalex-snapshot
HYDROFORMYLATION OF OLEFINS WITH RHODIUM CARBONYLS AS CATALYSTS. IV. MECHANISM OF THE REACTION
inferredcites →https://doi.org/10.1126/science.1074801openalex-snapshot
Internal Olefins to Linear Amines

What points at this work

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

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Triphenylphosphine-Derived Ligands for Rhodium-Catalyzed High Olefin Hydroformylations: From Traditional Molecules to Modern Cage Ligands
inferred← citeshttps://doi.org/10.1002/14356007.a22_157.pub3openalex-snapshot
Propanal
inferred← citeshttps://doi.org/10.1002/14356007.a22_173.pub3openalex-snapshot
Propanols
inferred← citeshttps://doi.org/10.1002/9783527695294.part3aopenalex-snapshot
References
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Confining Phosphanes Derived from Cyclodextrins for Efficient Regio‐ and Enantioselective Hydroformylation
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Confining Phosphanes Derived from Cyclodextrins for Efficient Regio‐ and Enantioselective Hydroformylation
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Understanding Rh‐catalysed Hydroformylation with Phosphite Ligands through Catalyst Speciation Analysis by Operando FlowNMR Spectroscopy
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An Operando FTIR Spectroscopic and Kinetic Study of Carbon Monoxide Pressure Influence on Rhodium‐Catalyzed Olefin Hydroformylation
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Impact of the P‐Ligand Concentration on the Formation of Hydroformylation Catalysts: An in situ FTIR Spectroscopic Study
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Palladium‐Catalyzed Alkoxycarbonylation of sec‐Benzylic Ethers
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Ambient Pressure Hydroformylation – A Key Step to Meso‐Alkyl BODIPYs
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Efficient and Recyclable RuCl3 ⋅ 3H2O Catalyst Modified with Ionic Diphosphine for the Alkoxycarbonylation of Aryl Halides
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Synthesis of fragrance compounds from acyclic monoterpenes: Rhodium catalyzed hydroformylation and tandem hydroformylation/acetalization of linalool and β-citronellene
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Phospholes as efficient ancillaries for the rhodium-catalyzed hydroformylation and hydroaminomethylation of estragole
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Hydroformylation of recalcitrating biorenewable compounds containing trisubstituted double bonds
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Hydroformylation and one-pot hydroformylation/epoxy ring cleavage of limonene oxide: A sustainable access to biomass-based multi-functional fragrances
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Production of diacetates from propenylphenols: A one-pot two-step approach involving hydroformylation/hydrogenation/O-acylation
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Tandem hydroformylation-acetalization of renewable terpenes and propenylbenzenes using glycerol: A potential route to fuels additives
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Adjacent MnOx clusters enhance the hydroformylation activity of rhodium single-atom catalysts
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New scents using eco-friendly solvents: Oxo synthesis of aldehydes from caryophyllane sesquiterpenes
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One-pot hydroformylation/O-acylation of propenylbenzenes for the synthesis of polyfunctionalized fragrances
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Novel fragrant aldehydes from (1R,5R)-sabinene: An experimental study supported by DFT calculations revealing an unusual hydroformylation mechanism
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Ethylene as a synthon in carbonylative synthesis
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Xantphos doped Rh/POPs-PPh3 catalyst for highly selective long-chain olefins hydroformylation: Chemical and DFT insights into Rh location and the roles of Xantphos and PPh3
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Heterogeneous Rh/CPOL-BP&P(OPh)3 catalysts for hydroformylation of 1-butene: The formation and evolution of the active species
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Phosphine-ligated Ir(III)-complex as a bi-functional catalyst for one-pot tandem hydroformylation-acetalization
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Enhanced regioselectivity in propylene hydroformylation using Xantphos-modified single-atom Rh/CeO2 catalyst
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Two-step one-pot Johnson-Claisen rearrangement/hydroformylation of renewable feedstocks
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Intramolecular C–H activation by air-stable Pt(II) phosphite complexes
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Hydroformylation of olefins by metals other than rhodium
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Composition of catalyst resting states of hydroformylation catalysts derived from bulky mono-phosphorus ligands, rhodium dicarbonyl acetylacetonate and syngas
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Development of highly electron-deficient and less sterically-hindered phosphine ligands possessing 1,3,5-triazinyl groups
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Hydroformylation of biomass-based hydroxyolefins in eco-friendly solvents: New fragrances from myrtenol and nopol
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Boosting the hydrolytic stability of phosphite ligand in hydroformylation by the construction of superhydrophobic porous framework
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Promotion of diphosphine ligands (PPh2(CH2) PPh2, n = 1, 2, 3, 5, 6) for supported Rh/SiO2 catalysts in heterogeneous ethene hydroformylation
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Oxo synthesis of novel fragrant aldehydes from biomass-based cis-jasmone and cis-jasmone lactone in green solvents
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Ionic Rh(I)-complexes containing π-accepting and hemilabile P,N-ligands as efficient catalysts for hydroformylation of 1-octene
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Promotion effect of water on hydroformylation of styrene and its derivatives with presence of amphiphilic zwitterionic phosphines
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Effect of positive-charges in diphosphino-imidazolium salts on the structures of Ir-complexes and catalysis for hydroformylation
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Highly efficient Rh(I)/tris-H8-binaphthyl monophosphite catalysts for hydroformylation of dicyclopentadiene to dialdehydes
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Enhancing the activity, selectivity, and recyclability of Rh/PPh3 system-catalyzed hydroformylation reactions through the development of a PPh3-derived quasi-porous organic cage as a ligand
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Displacement of P-Stereogenic Phosphiranes from Rhodium by CO in Hydroformylation Catalysis
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Cobalt-Catalyzed Carbonylative Synthesis of 4-Oxobutanoates from Formamide and Ethylene
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Insights into the Activity Screening and Hydroformylation Kinetics of Rh-Based Bimetallic Phosphides
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Interplay between Catalyst Complexes and Dormant States: In Situ Spectroscopic Investigations on a Catalyst System for Alkene Hydroformylation
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Cobalt-Catalyzed Hydroformylation under Mild Conditions in the Presence of Phosphine Oxides
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Rhodium catalyzed hydroformylation of nerolidol
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Phosphonium-based aminophosphines as bifunctional ligands for sequential catalysis of one-pot hydroformylation–acetalization of olefins
inferred← citeshttps://doi.org/10.1039/c5fd00195aopenalex-snapshot
Immobilization of a rhodium catalyst using a diphosphine-functionalized ionic liquid in RTIL for the efficient and recyclable biphasic hydroformylation of 1-octene
inferred← citeshttps://doi.org/10.1039/c5gc02127hopenalex-snapshot
Co-catalysis of a bi-functional ligand containing phosphine and Lewis acidic phosphonium for hydroformylation–acetalization of olefins
inferred← citeshttps://doi.org/10.1039/c6gc03096copenalex-snapshot
Efficient and recyclable Ir( i )-catalysts with the involvement of π-acceptor phosphines for N-alkylation of aryl amines with alcohols
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Anisole: a further step to sustainable hydroformylation
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Palladium-catalyzed carbonylations of highly substituted olefins using CO-surrogates
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The first one-pot metathesis–hydroformylation procedure: a straight synthesis of 2-arylpropanals from renewable 1-propenylbenzenes
inferred← citeshttps://doi.org/10.1039/d4dt02627fopenalex-snapshot
Modular synthesis of triphenylphosphine-derived cage ligands for rhodium-catalyzed hydroformylation applications
inferred← citeshttps://doi.org/10.1039/d4nj02288bopenalex-snapshot
In situ FTIR spectroscopic investigations on rhodium carbonyl complexes in the absence of phosphorus ligands under hydroformylation conditions
inferred← citeshttps://doi.org/10.1055/sos-sd-212-00003openalex-snapshot
1.1.1 Hydroformylation of Alkenes
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Experimental investigation of the complex liquid liquid equilibrium in the system pure/technical grade nonionic surfactant + water + oil
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PGMs IN THE LAB: New Diphosphines for Molecular and Nanoparticle Catalysis
inferred← citeshttps://doi.org/10.3390/molecules29102368openalex-snapshot
Monofluorophos–Metal Complexes: Ripe for Future Discoveries in Homogeneous Catalysis
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Phosphinocyclodextrins as confining units for catalytic metal centres. Applications to carbon–carbon bond forming reactions
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Novel Ir-Complexes for Hydroformylation of Olefins with H2O as the Hydrogen Source
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