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Phospholes as efficient ancillaries for the rhodium-catalyzed hydroformylation and hydroaminomethylation of estragole

https://doi.org/10.1016/j.apcata.2015.02.028
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/9780470132548.ch25openalex-snapshot
Dinuclear Methoxy, Cyclooctadiene, and Barrelene Complexes of Rhodium(I) and Iridium(I)
inferredcites →https://doi.org/10.1002/adsc.200700132openalex-snapshot
Hydroaminomethylation of n‐Alkenes in a Biphasic Ionic Liquid System
inferredcites →https://doi.org/10.1002/anie.198001841openalex-snapshot
3‐Phenylpropylamines, A New Class of Systemic Fungicides
inferredcites →https://doi.org/10.1002/anie.201301365openalex-snapshot
Continuous Gas‐Phase Hydroaminomethylation using Supported Ionic Liquid Phase Catalysts
inferredcites →https://doi.org/10.1002/anie.201402368openalex-snapshot
Phosphine‐ and Hydrogen‐Free: Highly Regioselective Ruthenium‐Catalyzed Hydroaminomethylation of Olefins
inferredcites →https://doi.org/10.1002/cctc.200900088openalex-snapshot
Fast and Selective Hydroaminomethylation Using Xanthene‐Based Amino‐Functionalized Ligands
inferredcites →https://doi.org/10.1002/cctc.201000411openalex-snapshot
Recent Advances in Amine Synthesis by Catalytic Hydroaminomethylation of Alkenes
inferredcites →https://doi.org/10.1002/cctc.201200057openalex-snapshot
Synthesis of Fragrance Ingredients by Tandem Hydroformylation‐Cyclization of Limonene Catalyzed by Rhodium Complexes and Pyridinium p ‐Toluenesulphonate
inferredcites →https://doi.org/10.1002/cctc.201200948openalex-snapshot
Synthesis of Fragrance Compounds from Biorenewables: Tandem Hydroformylation–Acetalization of Bicyclic Monoterpenes
inferredcites →https://doi.org/10.1002/chem.200600702openalex-snapshot
Highly Selective Hydroaminomethylation of Internal Alkenes To Give Linear Amines
inferredcites →https://doi.org/10.1002/chem.200601155openalex-snapshot
Hydroaminomethylation with Novel Rhodium–Carbene complexes: An Efficient Catalytic Approach to Pharmaceuticals
inferredcites →https://doi.org/10.1002/chem.201103073openalex-snapshot
Highly Regioselective Hydroaminomethylation of Terminal Olefins to Linear Amines Using Rh Complexes with a Tetrabi Phosphorus Ligand
inferredcites →https://doi.org/10.1002/chem.201103474openalex-snapshot
Interplay between Cationic and Neutral Species in the Rhodium‐Catalyzed Hydroaminomethylation Reaction
inferredcites →https://doi.org/10.1002/chem.201300899openalex-snapshot
Towards the Development of a Selective Ruthenium‐Catalyzed Hydroformylation of Olefins
inferredcites →https://doi.org/10.1002/ejlt.201300224openalex-snapshot
Diester monomers from methyl oleate and proline via tandem hydroaminomethylation‐esterification sequence with homogeneous catalyst recycling using TMS‐technique
inferredcites →https://doi.org/10.1002/jlac.19535820107openalex-snapshot
Carbonylierung VI. Synthesen mit Metallcarbonylwasserstoffen
inferredcites →https://doi.org/10.1007/s11244-010-9574-9openalex-snapshot
Synthesis of Fexofenadine via Rhodium-Catalyzed Hydroaminomethylation
inferredcites →https://doi.org/10.1007/s11244-013-0184-1openalex-snapshot
Biocatalytic Approaches to the Synthesis of Enantiomerically Pure Chiral Amines
inferredcites →https://doi.org/10.1016/0304-5102(89)80226-3openalex-snapshot
Phospholes as ligands for rhodium systems in homogeneously catalysed hydroformylation reactions
inferredcites →https://doi.org/10.1016/0304-5102(89)85007-2openalex-snapshot
Phospholes as ligands for rhodium systems in homogeneously-catalysed hydroformylation reactions
inferredcites →https://doi.org/10.1016/j.apcata.2007.04.014openalex-snapshot
Rhodium catalyzed hydroformylation of monoterpenes containing a sterically encumbered trisubstituted endocyclic double bond under mild conditions
inferredcites →https://doi.org/10.1016/j.apcata.2010.03.045openalex-snapshot
Tandem hydroformylation-acetalization of para-menthenic terpenes under non-acidic conditions
inferredcites →https://doi.org/10.1016/j.apcata.2011.10.021openalex-snapshot
An efficient method for the transformation of naturally occurring monoterpenes into amines through rhodium-catalyzed hydroaminomethylation
inferredcites →https://doi.org/10.1016/j.apcata.2012.08.033openalex-snapshot
Hydroaminomethylation of eugenol with di-n-butylamine catalyzed by rhodium complexes: Bringing light on the promoting effect of Brönsted acids
inferredcites →https://doi.org/10.1016/j.apcata.2012.12.021openalex-snapshot
Rhodium complex encapsulated functionalized hexagonal mesoporous silica for heterogeneous hydroaminomethylation
inferredcites →https://doi.org/10.1016/j.apcata.2013.06.037openalex-snapshot
Synthesis of fragrance compounds from acyclic monoterpenes: Rhodium catalyzed hydroformylation and tandem hydroformylation/acetalization of linalool and β-citronellene
inferredcites →https://doi.org/10.1016/j.apcata.2014.01.002openalex-snapshot
Rhodium exchanged ETS-10 and ETS-4: Efficient heterogeneous catalyst for hydroaminomethylation
inferredcites →https://doi.org/10.1016/j.ica.2005.12.039openalex-snapshot
Rhodium-diphosphite catalysed hydroformylation of allylbenzene and propenylbenzene derivatives
inferredcites →https://doi.org/10.1016/j.jcat.2012.11.031openalex-snapshot
Bulky monophosphite ligands for ethene hydroformylation
inferredcites →https://doi.org/10.1016/j.molcata.2005.06.020openalex-snapshot
Hydroaminomethylation in thermomorphic solvent systems
inferredcites →https://doi.org/10.1016/j.tet.2013.10.014openalex-snapshot
Construction of 3-arylpropylamines using Heck arylations. The total synthesis of cinacalcet hydrochloride, alverine, and tolpropamine
inferredcites →https://doi.org/10.1016/j.tetlet.2003.11.044openalex-snapshot
Highly selective synthesis of hydrazones and indoles from olefins
inferredcites →https://doi.org/10.1016/j.tetlet.2005.08.107openalex-snapshot
An improved protocol for the selective hydroaminomethylation of arylethylenes
inferredcites →https://doi.org/10.1016/j.tetlet.2010.02.145openalex-snapshot
A highly efficient method for the hydroaminomethylation of long-chain alkenes under aqueous, biphasic conditions
inferredcites →https://doi.org/10.1016/s0040-4020(01)97949-9openalex-snapshot
On the mechanism of the nickel-catalysed regioselective cyclodimerization of isoprene
inferredcites →https://doi.org/10.1016/s0040-4020(99)00536-0openalex-snapshot
One-pot synthesis of pharmacologically active diamines via rhodium-catalysed carbonylative hydroaminomethylation of heterocyclic allylic amines
inferredcites →https://doi.org/10.1021/cr60307a002openalex-snapshot
Steric effects of phosphorus ligands in organometallic chemistry and homogeneous 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/ja01504a021openalex-snapshot
Novel Heterocyclopentadienes. II
inferredcites →https://doi.org/10.1021/ja310054dopenalex-snapshot
Chemical Plants: High-Value Molecules from Essential Oils
inferredcites →https://doi.org/10.1021/ja312271copenalex-snapshot
Efficient and Regioselective Ruthenium-catalyzed Hydro-aminomethylation of Olefins
inferredcites →https://doi.org/10.1021/jo402632sopenalex-snapshot
Regioselective Hydroaminomethylation of Vinylarenes by a Sol–Gel Immobilized Rhodium Catalyst
inferredcites →https://doi.org/10.1021/ol050848yopenalex-snapshot
Synthesis of Biologically Active Amines via Rhodium−Bisphosphite-Catalyzed Hydroaminomethylation
inferredcites →https://doi.org/10.1021/ol202848aopenalex-snapshot
Highly Regioselective Isomerization–Hydroaminomethylation of Internal Olefins Catalyzed by Rh Complex with Tetrabi-Type Phosphorus Ligands
inferredcites →https://doi.org/10.1021/ol303483topenalex-snapshot
Cascade Synthesis of Fenpiprane and Related Pharmaceuticals via Rhodium-Catalyzed Hydroaminomethylation
inferredcites →https://doi.org/10.1021/om300814fopenalex-snapshot
N-Heterocyclic Carbenes with aN-2,4-Dinitrophenyl Substituent: Comparison with PPh3and IPr
inferredcites →https://doi.org/10.1021/om301244mopenalex-snapshot
Gold Phosphole Complexes as Efficient Catalysts for Alkyne Activation
inferredcites →https://doi.org/10.1021/om800451topenalex-snapshot
Hydroformylation of Monoterpenic Polyenes: Effect of the Conjugation of Double Bonds on Reactivity
inferredcites →https://doi.org/10.1039/b702497eopenalex-snapshot
Rhodium(i)-catalyzed hydroaminomethylation of 2-isopropenylanilines as a novel route to 1,2,3,4-tetrahydroquinolines
inferredcites →https://doi.org/10.1039/c1cy00026hopenalex-snapshot
On the rate-determining step and the ligand electronic effects in rhodium catalysed hydrogenation of enamines and the hydroaminomethylation of alkenes
inferredcites →https://doi.org/10.1039/c2dt12400aopenalex-snapshot
Interception of a Rh(I)–Rh(III) dinuclear trihydride complex revealing the dihydrogen activation by [Rh(CO)2{(R,R)-Ph–BPE}]
inferredcites →https://doi.org/10.1039/c3cy01069dopenalex-snapshot
Rhodium-catalyzed regioselective hydroaminomethylation of terminal olefins with pyrrole-based tetraphosphorus ligands
inferredcites →https://doi.org/10.1039/c4ob00620hopenalex-snapshot
Recent advances in catalytic C–N bond formation: a comparison of cascade hydroaminomethylation and reductive amination reactions with the corresponding hydroamidomethylation and reductive amidation reactions
inferredcites →https://doi.org/10.1039/jr9650002184openalex-snapshot
389. Synthesis and chemistry of phospholes
inferredcites →https://doi.org/10.1080/00945718708059436openalex-snapshot
Improved Syntheses of Tetraphenylphosphonium Bromide and 1-Phenyldibenzophosphole

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
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Rhodium‐Catalyzed Carbonylations
inferred← citeshttps://doi.org/10.1002/aoc.4478openalex-snapshot
Rhodium/Phosphine catalysed selective hydroformylation of biorenewable olefins
inferred← citeshttps://doi.org/10.1002/aoc.70111openalex-snapshot
Isomerization and Hydroformylation of Long‐Chain Olefins Promoted by N^O Bidentate Rh(I) Catalysts Precursors Bearing Salicylaldimine and Naphthaldimine Supporting Ligands
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Decreasing Side Products and Increasing Selectivity in the Tandem Hydroformylation/Acyloin Reaction
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Renewable Surfactants through the Hydroaminomethylation of Terpenes
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Hydroaminomethylation of Natural Allylic and Homoallylic Alcohols: A Ligand‐Controlled Route to New Amines
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2‐Arylpropylamines from 1‐Propenylbenzenes in a New One‐Pot Metathesis–Hydroaminomethylation Protocol
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Direct Synthesis of an α,ω‐Diester from 2,7‐Octadienol as Bulk Feedstock in Three Tandem Catalytic Steps
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Carbon Monoxide as C1 Building Block in Fine Chemical Synthesis†
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Catalyst recycling in the hydroaminomethylation of methyl oleate: A route to novel polyamide monomers
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Tandem Rhodium Carbonylation Reactions
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Characterizing the Metal–Ligand Bond Strength via Vibrational Spectroscopy: The Metal–Ligand Electronic Parameter (MLEP)
inferred← citeshttps://doi.org/10.1016/b978-0-12-812284-6.00004-4openalex-snapshot
N -Alkyl Amine Synthesis by Hydroaminomethylation
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Sustainable route to biomass-based amines: rhodium catalyzed hydroaminomethylation in green solvents
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Tandem hydroformylation-acetalization of renewable terpenes and propenylbenzenes using glycerol: A potential route to fuels additives
inferred← citeshttps://doi.org/10.1016/j.ccr.2025.216990openalex-snapshot
Hydroformylation of specific substrates as a perspective route to monomers and valuable bifunctional compounds
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A rational synthetic approach to 2,3,4,5-tetraphenyl-1-monophosphole and its derivatives
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Replacing syngas by formic acid and acetic anhydride with advantages: tandem carbonylation of renewable terpenes and propenylbenzenes
inferred← citeshttps://doi.org/10.1016/j.tet.2017.03.023openalex-snapshot
Sequential reactions from catalytic hydroformylation toward the synthesis of amino compounds
inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00667openalex-snapshot
Tandem Hydroaminomethylation Reaction to Synthesize Amines from Alkenes
inferred← citeshttps://doi.org/10.1021/acs.chemrev.9b00462openalex-snapshot
New Strategies for the Transition-Metal Catalyzed Synthesis of Aliphatic Amines
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00359openalex-snapshot
Formal Transition-Metal-Catalyzed Phosphole C–H Activation for the Synthesis of Pentasubstituted Phospholes
inferred← citeshttps://doi.org/10.1039/c4cy01701copenalex-snapshot
Phosphole-based ligands in catalysis
inferred← citeshttps://doi.org/10.1039/c5qo00397kopenalex-snapshot
Gold( i ) catalyzed [1,3] O → C rearrangement of benzylvinyl ethers
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Recent progress in rhodium-catalyzed hydroaminomethylation
inferred← citeshttps://doi.org/10.1039/c7dt00178aopenalex-snapshot
Generalization of the Tolman electronic parameter: the metal–ligand electronic parameter and the intrinsic strength of the metal–ligand bond
inferred← citeshttps://doi.org/10.1039/c8dt02208aopenalex-snapshot
Novel enantiopure monophospholes: synthesis, spatial and electronic structure, photophysical characteristics and conjugation effects
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Hydroformylation, hydroaminomethylation and related tandem reactions of bio-derived renewable olefins: a step closer to sustainability
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9.14.5 Phospholes (Update 2024)
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Nanopartículas de Ródio: componentes para a preparação de catalisadores para reações de hidroformilação de olefinas
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Valorization of Biomass Derived Terpene Compounds by Catalytic Amination
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(Bi)metallic nanoparticles in glycerol : synthesis, characterization and catalytic aplications
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