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New anionic rhodium complexes as catalysts for the reduction of acetophenone and its derivatives
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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/(sici)1521-3773(19980817)37:15<1986::aid-anie1986>3.0.co;2-zopenalex-snapshot
Reduction of Carbonyl Compounds with Chiral Oxazaborolidine Catalysts: A New Paradigm for Enantioselective Catalysis and a Powerful New Synthetic Method
inferredcites →https://doi.org/10.1002/9783527609451openalex-snapshot
N‐Heterocyclic Carbenes in Synthesis
inferredcites →https://doi.org/10.1002/adsc.200900246openalex-snapshot
A Convenient and Efficient Rhenium‐Catalyzed Hydrosilylation of Ketones and Aldehydes
inferredcites →https://doi.org/10.1002/anie.200462250openalex-snapshot
Hydroamination/Hydrosilylation Sequence Catalyzed by Titanium Complexes
inferredcites →https://doi.org/10.1002/anie.200602668openalex-snapshot
Polishing a Diamond in the Rough: “CuH” Catalysis with Silanes
inferredcites →https://doi.org/10.1002/chem.201504553openalex-snapshot
Cover Picture: Sandmeyer‐Type Trifluoromethylthiolation and Trifluoromethylselenolation of (Hetero)Aromatic Amines Catalyzed by Copper (Chem. Eur. J. 1/2016)
inferredcites →https://doi.org/10.1002/chem.201602760openalex-snapshot
Rhodium‐Catalyzed Dehydrogenative Silylation of Acetophenone Derivatives: Formation of Silyl Enol Ethers versus Silyl Ethers
inferredcites →https://doi.org/10.1002/cite.200490405openalex-snapshot
Buchbesprechung: Chemistry in Alternative Reaction Media. Von D. J. Adams, P. J. Dyson, S. J. Travener.
inferredcites →https://doi.org/10.1002/ejic.200801163openalex-snapshot
Rhodium(I) Complexes of New Ferrocenyl Benzimidazol‐2‐ylidene Ligands: The Importance of the Chelating Effect for Ketone Hydrosilylation Catalysis
inferredcites →https://doi.org/10.1002/ejoc.201000648openalex-snapshot
Formamidines – Versatile Ligands for Zinc‐Catalyzed Hydrosilylation and Iron‐Catalyzed Epoxidation Reactions
inferredcites →https://doi.org/10.1007/978-1-4020-8172-9openalex-snapshot
Hydrosilylation : a comprehensive review on recent advances
inferredcites →https://doi.org/10.1016/0022-328x(90)85111-bopenalex-snapshot
Asymmetric catalysis LVI . Enantioselective hydrosilylation of acetophenone with a rhodium/picolineoxazoline catalyst 1:1
inferredcites →https://doi.org/10.1016/0040-4039(92)88150-4openalex-snapshot
Asymmetric intramolecular hydrosilylation of hydroxyketones
inferredcites →https://doi.org/10.1016/0277-5387(95)00244-mopenalex-snapshot
Structure of bis-(1,5-cyclooctadiene)-di-μ-(trimethylsilyloxy)dirhodium(I)
inferredcites →https://doi.org/10.1016/0277-5387(96)00156-8openalex-snapshot
The structure and some reactions of di-μ-trimethylsilyloxy-bis-(norborna-2,5-diene)-dirhodium(I)
inferredcites →https://doi.org/10.1016/j.apcata.2012.10.033openalex-snapshot
Diallyldimethylammonium and trimethylvinylammonium ionic liquids—Synthesis and application to catalysis
inferredcites →https://doi.org/10.1016/j.ica.2017.07.055openalex-snapshot
Rhodium(I) N-heterocyclic carbene complexes as catalysts for the hydrosilylation of aromatic ketones with triethylsilane
inferredcites →https://doi.org/10.1016/j.molliq.2016.11.123openalex-snapshot
A review of ionic liquids: Applications towards catalytic organic transformations
inferredcites →https://doi.org/10.1016/s0022-328x(00)86954-5openalex-snapshot
Reduction of carbonyl compounds via hydrosilylation
inferredcites →https://doi.org/10.1016/s0040-4039(00)00652-3openalex-snapshot
An efficient protocol for the reduction of ketones with tin(II) complexes and PMHS
inferredcites →https://doi.org/10.1016/s0040-4039(00)00818-2openalex-snapshot
KO2/crown ether: a novel catalytic system for the hydrosilation and Tishchenko reaction of aromatic aldehydes
inferredcites →https://doi.org/10.1016/s1566-7367(03)00112-2openalex-snapshot
Addition of silanes to benzaldehyde catalyzed by KF loaded on alumina
inferredcites →https://doi.org/10.1021/acs.organomet.5b00506openalex-snapshot
Hydrosilylation of Aldehydes and Ketones Catalyzed by a Terminal Zinc Hydride Complex, [κ3-Tptm]ZnH
inferredcites →https://doi.org/10.1021/acs.organomet.5b00630openalex-snapshot
Iron-Catalyzed Hydrosilylation of Aldehydes and Ketones under Solvent-Free Conditions
inferredcites →https://doi.org/10.1021/acs.organomet.6b00765openalex-snapshot
Efficient Hydrosilylation of Acetophenone with a New Anthraquinonic Amide-Based Iron Precatalyst
inferredcites →https://doi.org/10.1021/ar700134qopenalex-snapshot
Asymmetric Transfer Hydrogenation of Ketones with Bifunctional Transition Metal-Based Molecular Catalysts
inferredcites →https://doi.org/10.1021/ar7001655openalex-snapshot
Copper, Silver, and Gold Complexes in Hydrosilylation Reactions
inferredcites →https://doi.org/10.1021/ar9002202openalex-snapshot
Toward Understanding the Origin of Positive Effects of Ionic Liquids on Catalysis: Formation of More Reactive Catalysts and Stabilization of Reactive Intermediates and Transition States in Ionic Liquids
inferredcites →https://doi.org/10.1021/cs200571vopenalex-snapshot
Rhodium-Catalyzed Hydrosilylation of Ketones: Catalyst Development and Mechanistic Insights
inferredcites →https://doi.org/10.1021/ja0042074openalex-snapshot
σ−π Chelation-Controlled Stereoselective Hydrosilylation of Ketones
inferredcites →https://doi.org/10.1021/ja011316popenalex-snapshot
Lewis Acid Catalyzed Stereoselective Carbosilylation. Intramolecular trans-Vinylsilylation and trans-Arylsilylation of Unactivated Alkynes
inferredcites →https://doi.org/10.1021/ja029498qopenalex-snapshot
Reversing the Role of the Metal−Oxygen π-Bond. Chemoselective Catalytic Reductions with a Rhenium(V)-Dioxo Complex
inferredcites →https://doi.org/10.1021/ja074477nopenalex-snapshot
Analysis of an Unprecedented Mechanism for the Catalytic Hydrosilylation of Carbonyl Compounds
inferredcites →https://doi.org/10.1021/ja402480vopenalex-snapshot
Electron-Rich N-Heterocyclic Silylene (NHSi)–Iron Complexes: Synthesis, Structures, and Catalytic Ability of an Isolable Hydridosilylene–Iron Complex
inferredcites →https://doi.org/10.1021/om034285aopenalex-snapshot
(NHC)Cu I (NHC = N-Heterocyclic Carbene) Complexes as Efficient Catalysts for the Reduction of Carbonyl Compounds
inferredcites →https://doi.org/10.1039/b110838gopenalex-snapshot
A short history of ionic liquids—from molten salts to neoteric solvents
inferredcites →https://doi.org/10.1039/b210144kopenalex-snapshot
Direct Zn–diamine promoted reduction of CO and CN bonds by polymethylhydrosiloxane in methanol
inferredcites →https://doi.org/10.1039/b414145hopenalex-snapshot
[MoO 2 Cl 2 ] as catalyst for hydrosilylation of aldehydes and ketones
inferredcites →https://doi.org/10.1039/b819310jopenalex-snapshot
Hydrosilylation of functionalised olefins catalysed by rhodium siloxide complexes in ionic liquids
inferredcites →https://doi.org/10.1039/c0cc05733aopenalex-snapshot
Homogeneous catalysis using iron complexes: recent developments in selective reductions
inferredcites →https://doi.org/10.1039/c3972000938aopenalex-snapshot
Rhodium complex catalysed hydrosilylation of carbonyl compounds
inferredcites →https://doi.org/10.1039/c3cs60310eopenalex-snapshot
Halometallate ionic liquids – revisited
inferredcites →https://doi.org/10.1039/c4cy01556hopenalex-snapshot
Orthometallation of N-substituents at the NHC ligand of [Rh(Cl)(COD)(NHC)] complexes: its role in the catalytic hydrosilylation of ketones
inferredcites →https://doi.org/10.1039/c5cc00612kopenalex-snapshot
Iron-catalyzed asymmetric hydrosilylation of ketones
inferredcites →https://doi.org/10.1039/c8ra05251dopenalex-snapshot
The effect of the morpholinium ionic liquid anion on the catalytic activity of Rh (or Pt) complex–ionic liquid systems in hydrosilylation processes
inferredcites →https://doi.org/10.1246/bcsj.80.2365openalex-snapshot
Syntheses, Structures, and Properties of a Series of Metal Ion-Containing Dialkylimidazolium Ionic Liquids
inferredcites →https://doi.org/10.2134/jeq2004.2388openalex-snapshot
Chemistry in Alternative Reaction Media
inferredcites →https://doi.org/10.3390/molecules21091115openalex-snapshot
Ionic Liquids as Solvents for Rhodium and Platinum Catalysts Used in Hydrosilylation Reaction
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4673735openalex-extracted
Chlororhodate Ionic Liquids as a New Type of Heterogeneous Catalyst for Hydrosilylation Processes
inferred← citeshttps://doi.org/10.1002/chem.202103099openalex-snapshot
Rh(I)/(III)‐N‐Heterocyclic Carbene Complexes: Effect of Steric Confinement Upon Immobilization on Regio‐ and Stereoselectivity in the Hydrosilylation of Alkynes
inferred← citeshttps://doi.org/10.1002/cphc.202200391openalex-snapshot
Formation and Surface Behavior of Pt and Pd Complexes with Ligand Systems Derived from Nitrile‐functionalized Ionic Liquids Studied by XPS
inferred← citeshttps://doi.org/10.1007/3418_2023_103openalex-snapshot
Catalysis of Hydrosilylation Processes with the Participation of Ionic Liquids
inferred← citeshttps://doi.org/10.1016/j.poly.2021.115564openalex-snapshot
The saga of rhodium(III) nitrate complexes and their speciation in solution: An integrated experimental and quantum chemical study
inferred← citeshttps://doi.org/10.1016/j.poly.2023.116371openalex-snapshot
Rhodium and iridium NHC complexes from chiral NHC precursors: Synthesis, structure, transfer hydrogenation catalysis and method validation
inferred← citeshttps://doi.org/10.1039/d2cp02771bopenalex-snapshot
Being negative can be positive: metal oxide anions promise more selective methane to methanol conversion
inferred← citeshttps://doi.org/10.3390/catal14120943openalex-snapshot
Anionic Rhodium Complexes as Very Active Catalysts for Hydro-Silylation Reactions
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