On the public citation graph
Transfer Hydrogenation of Acetophenone Catalyzed by Half-Sandwich Ruthenium(II) Complexes Containing Amino Amide Ligands. Detection of the Catalytic Intermediates by Electrospray Ionization Mass Spectrometry
0 signed · 151 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1521-3765(19990503)5:5<1544::aid-chem1544>3.0.co;2-topenalex-snapshot
Trimerisation of the Cationic Fragments [(η-ring)M(Aa)]+ ((η-ring) M=(η5-C5Me5)Rh, (η5-C5Me5)Ir, (η6-p-MeC6H4iPr)Ru; Aa=α-amino acidate) with Chiral Self-Recognition: Synthesis, Characterisation, Solution Studies and Catalytic Reactions of the Trimers [{(η-ring)M(Aa)}3](BF4)3
inferredcites →https://doi.org/10.1002/1521-3765(20000804)6:15<2818::aid-chem2818>3.0.co;2-qopenalex-snapshot
Chiral Induction Effects in Ruthenium(II) Amino Alcohol Catalysed Asymmetric Transfer Hydrogenation of Ketones: An Experimental and Theoretical Approach
inferredcites →https://doi.org/10.1002/1521-3765(20010202)7:3<591::aid-chem591>3.0.co;2-iopenalex-snapshot
Probing the Reactivity of Oxomanganese−Salen Complexes: An Electrospray Tandem Mass Spectrometric Study of Highly Reactive Intermediates
inferredcites →https://doi.org/10.1002/1521-3765(20010302)7:5<1014::aid-chem1014>3.0.co;2-xopenalex-snapshot
New Auxiliaries for Copper-Catalyzed Asymmetric Michael Reactions: Generation of Quaternary Stereocenters at Room Temperature
inferredcites →https://doi.org/10.1002/1521-3773(20010105)40:1<40::aid-anie40>3.0.co;2-5openalex-snapshot
Asymmetric Catalysis by Architectural and Functional Molecular Engineering: Practical Chemo- and Stereoselective Hydrogenation of Ketones
inferredcites →https://doi.org/10.1002/1521-3773(20010803)40:15<2818::aid-anie2818>3.0.co;2-yopenalex-snapshot
CH/π Attraction: The Origin of Enantioselectivity in Transfer Hydrogenation of Aromatic Carbonyl Compounds Catalyzed by Chiralη6-Arene-Ruthenium(II) Complexes
inferredcites →https://doi.org/10.1002/1615-4169(200207)344:5<499::aid-adsc499>3.0.co;2-ropenalex-snapshot
On the Sense of the Enantioselection in Hydrogen Transfer Reactions from 2-Propanol to Ketones
inferredcites →https://doi.org/10.1002/9780470132524.ch16openalex-snapshot
16. (η 6 ‐Hexamethylbenzene)Ruthenium Complexes
inferredcites →https://doi.org/10.1002/anie.199702851openalex-snapshot
The Catalyst Precursor, Catalyst, and Intermediate in the Ru II ‐Promoted Asymmetric Hydrogen Transfer between Alcohols and Ketones
inferredcites →https://doi.org/10.1002/anie.200200560openalex-snapshot
Electrospray Ionization Tandem Mass Spectrometry in High‐Throughput Screening of Homogeneous Catalysts
inferredcites →https://doi.org/10.1002/aoc.216openalex-snapshot
α‐Amino acid: an effective ligand for asymmetric catalysis of transfer hydrogenation of ketones
inferredcites →https://doi.org/10.1002/aoc.590090304openalex-snapshot
Amino‐Acids, peptides and their derivatives: Powerful chiral ligands for metal‐catalyzed asymmetric syntheses
inferredcites →https://doi.org/10.1002/chem.200305553openalex-snapshot
Highly Enantioselective Ruthenium‐Catalyzed Reduction of Ketones Employing Readily Available Peptide Ligands
inferredcites →https://doi.org/10.1016/0022-328x(84)80341-1openalex-snapshot
Asymmetric synthesis of cyclopropane carboxylates: Catalysis of diazoacetate reactions by copper(II) Schiff base complexes derived from α-amino acids
inferredcites →https://doi.org/10.1016/0223-5234(87)90062-6openalex-snapshot
Asymmetric synthesis, construction of chiral molecules using amino acids
inferredcites →https://doi.org/10.1016/j.tet.2004.01.020openalex-snapshot
Recent development of peptide coupling reagents in organic synthesis
inferredcites →https://doi.org/10.1016/j.tetasy.2004.05.025openalex-snapshot
The importance of 1,2-anti-disubstitution in monotosylated diamine ligands for ruthenium(II)-catalysed asymmetric transfer hydrogenation
inferredcites →https://doi.org/10.1016/s0010-8545(03)00024-9openalex-snapshot
[(Cy)Ru(LL*)Cl] and related half-sandwich compounds—two diastereomers in the same single crystal
inferredcites →https://doi.org/10.1016/s0022-328x(00)89228-1openalex-snapshot
Asymmetric hydrogenation of acetophenone with rhodium(I) complexes of new chiral phosphines derived from amino acids. An unusual modification of the catalyst system
inferredcites →https://doi.org/10.1016/s0022-328x(99)00433-7openalex-snapshot
Enantioselective hydride transfer hydrogenation of ketones catalyzed by [(η6-p-cymene)Ru(amino acidato)Cl] and [(η6-p-cymene)Ru(amino acidato)]3(BF4)3 complexes
inferredcites →https://doi.org/10.1016/s0040-4039(01)00914-5openalex-snapshot
Use of amino amides derived from proline as chiral ligands in the ruthenium(II)-catalyzed transfer hydrogenation reaction of ketones
inferredcites →https://doi.org/10.1016/s0040-4039(01)02132-3openalex-snapshot
Use of surfactants in water-soluble ruthenium(II) complex-catalyzed asymmetric hydrogen-transfer reduction of aromatic ketones
inferredcites →https://doi.org/10.1016/s0040-4039(03)01705-2openalex-snapshot
Nickel complexes from α-amino amides as efficient catalysts for the enantioselective Et2Zn addition to benzaldehyde
inferredcites →https://doi.org/10.1016/s0957-4166(99)00216-5openalex-snapshot
Asymmetric transfer hydrogenation of CO and CN bonds
inferredcites →https://doi.org/10.1021/ar9502341openalex-snapshot
Asymmetric Transfer Hydrogenation Catalyzed by Chiral Ruthenium Complexes
inferredcites →https://doi.org/10.1021/cr00013a015openalex-snapshot
Asymmetric hydrogen transfer reactions promoted by homogeneous transition metal catalysts
inferredcites →https://doi.org/10.1021/ja00133a037openalex-snapshot
Asymmetric Transfer Hydrogenation of Aromatic Ketones Catalyzed by Chiral Ruthenium(II) Complexes
inferredcites →https://doi.org/10.1021/ja030272copenalex-snapshot
Mechanism of Asymmetric Hydrogenation of Ketones Catalyzed by BINAP/1,2-Diamine−Ruthenium(II) Complexes
inferredcites →https://doi.org/10.1021/ja046157zopenalex-snapshot
Detection of Transient Radical Cations in Electron Transfer-Initiated Diels−Alder Reactions by Electrospray Ionization Mass Spectrometry
inferredcites →https://doi.org/10.1021/ja954126lopenalex-snapshot
Ruthenium(II)-Catalyzed Asymmetric Transfer Hydrogenation of Ketones Using a Formic Acid−Triethylamine Mixture
inferredcites →https://doi.org/10.1021/ja971570aopenalex-snapshot
Asymmetric Transfer Hydrogenation of α, β-Acetylenic Ketones
inferredcites →https://doi.org/10.1021/ja980004sopenalex-snapshot
Ziegler−Natta-like Olefin Oligomerization by Alkylzirconocene Cations in an Electrospray Ionization Tandem Mass Spectrometer
inferredcites →https://doi.org/10.1021/ja991638hopenalex-snapshot
The Metal−Ligand Bifunctional Catalysis: A Theoretical Study on the Ruthenium(II)-Catalyzed Hydrogen Transfer between Alcohols and Carbonyl Compounds
inferredcites →https://doi.org/10.1021/jo00218a004openalex-snapshot
L-Cysteine-, L-methionine- and D-penicillamine-derived ligands for transition metal catalyzed carbon-carbon bond-forming reactions
inferredcites →https://doi.org/10.1021/jo970405aopenalex-snapshot
(1R,2S)-(+)-cis-1-Amino-2-indanol: An Effective Ligand for Asymmetric Catalysis of Transfer Hydrogenations of Ketones
inferredcites →https://doi.org/10.1021/jo972082oopenalex-snapshot
(1S,3R,4R)-2-Azanorbornylmethanol, an Efficient Ligand for Ruthenium-Catalyzed Asymmetric Transfer Hydrogenation of Ketones
inferredcites →https://doi.org/10.1021/jo991615lopenalex-snapshot
Versatile Chiral Bidentate Ligands Derived from α-Amino Acids: Synthetic Applications and Mechanistic Considerations in the Palladium-Mediated Asymmetric Allylic Substitutions
inferredcites →https://doi.org/10.1021/jo991914aopenalex-snapshot
2-Azanorbornyl Alcohols: Very Efficient Ligands for Ruthenium-Catalyzed Asymmetric Transfer Hydrogenation of Aromatic Ketones
inferredcites →https://doi.org/10.1021/ol990098qopenalex-snapshot
A Chiral Rhodium Complex for Rapid Asymmetric Transfer Hydrogenation of Imines with High Enantioselectivity
inferredcites →https://doi.org/10.1021/om010644vopenalex-snapshot
Catalysts for the Asymmetric Transfer Hydrogenation of Ketones Derived from l -Prolinamide and (p-CymeneRuCl2)2or (Cp*RhCl2)2
inferredcites →https://doi.org/10.1021/om9903689openalex-snapshot
pH-Dependent Transfer Hydrogenation of Water-Soluble Carbonyl Compounds with [Cp*IrIII(H2O)3]2+(Cp* =η5-C5Me5) as a Catalyst Precursor and HCOONa as a Hydrogen Donor in Water
inferredcites →https://doi.org/10.1039/a908098hopenalex-snapshot
The detection of intermediates in the ruthenium(ii) catalysed asymmetric hydrogenation of ketones using electrospray ionisation mass spectrometry
inferredcites →https://doi.org/10.1039/b106130popenalex-snapshot
The first Ru(II)-catalysed asymmetric hydrogen transfer reduction of aromatic ketones in aqueous media.
inferredcites →https://doi.org/10.1039/b206471eopenalex-snapshot
Novel simple and highly modular ligands for efficient asymmetric transfer-hydrogenation of ketones
inferredcites →https://doi.org/10.1039/b415560bopenalex-snapshot
Aggregation in solution of neutral half-sandwich Ru(ii) precatalysts for transfer hydrogenation
inferredcites →https://doi.org/10.1039/cc9960000233openalex-snapshot
Amino alcohol effects on the ruthenium(II)-catalysed asymmetric transfer hydrogenation of ketones in propan-2-ol
inferredcites →https://doi.org/10.1039/p19870000071openalex-snapshot
Asymmetric oxidation of sulphides to sulphoxides catalysed by titanium complexes of N-salicylidene-L-amino acids
inferredcites →https://doi.org/10.1055/s-1991-20798openalex-snapshot
Asymmetric Cyanosilylation of Aldehydes Promoted by a Novel Chiral Lewis Acid, Organoaluminum Complex of Acyclic Dipeptide Esters or α-Amino Amides Containing a Phenolic Schiff Base
inferredcites →https://doi.org/10.1246/cl.1985.391openalex-snapshot
STERIC EFFECTS OF CHIRAL LIGANDS IN A NEW TYPE OF ALDOL CONDENSATIONS CATALYZED BY ZINC(II) COMPLEXES OF α-AMINO ACID ESTERS
inferredcites →https://doi.org/10.1246/cl.1998.491openalex-snapshot
α-Amino acidate-Ru(II) Catalysts for Asymmetric Transfer Hydrogenation: First Utilization of α-Amino Acids as an Efficient Ligand
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.4766396openalex-extracted
A Comparative Study of the Catalytic Activity of Ruo2/Ce0.85zr0.15o2 in Oxidation Reactions and Transfer Hydrogention: Impact of Surface Modification with Alkali Ions
inferred← citeshttps://doi.org/10.1002/adsc.200700345openalex-snapshot
Rhodium‐Catalyzed Asymmetric Transfer Hydrogenation of Aryl Alkyl Ketones Employing Ligands Derived from Amino Acids
inferred← citeshttps://doi.org/10.1002/adsc.201700134openalex-snapshot
Amine Activation: N‐Arylamino Acid Amide Synthesis from Isothioureas and Amino Acids
inferred← citeshttps://doi.org/10.1002/ange.201204921openalex-snapshot
Die N‐H‐Funktion in der metallorganischen Katalyse
inferred← citeshttps://doi.org/10.1002/anie.201204921openalex-snapshot
The NH Functional Group in Organometallic Catalysis
inferred← citeshttps://doi.org/10.1002/aoc.1594openalex-snapshot
New chiral phosphinite ligands with C2‐symmetric axis and their possible applications in Ru‐catalyzed asymmetric transfer hydrogenation
inferred← citeshttps://doi.org/10.1002/aoc.1753openalex-snapshot
Applications of transition metal complexes containing aminophosphine ligand to transfer hydrogenation of ketones
inferred← citeshttps://doi.org/10.1002/aoc.1779openalex-snapshot
Synthesis of new boron complexes: application to transfer hydrogenation of acetophenone derivatives
inferred← citeshttps://doi.org/10.1002/aoc.1853openalex-snapshot
A modular design of metal catalysts for the transfer hydrogenation of aromatic ketones
inferred← citeshttps://doi.org/10.1002/aoc.2823openalex-snapshot
Temperature‐tuned enantioselectivity in transfer hydrogenation: preparation and catalytic property of amino acid‐modified benzimidazole
inferred← citeshttps://doi.org/10.1002/aoc.3096openalex-snapshot
Novel cyclohexyl‐based aminophosphine ligands and use of their Ru(II) complexes in transfer hydrogenation of ketones
inferred← citeshttps://doi.org/10.1002/aoc.3202openalex-snapshot
The application of tunable tridendate P‐based ligands for the Ru(II)‐catalysed transfer hydrogenation of various ketones
inferred← citeshttps://doi.org/10.1002/aoc.3442openalex-snapshot
Ruthenium(II) complexes derived from 2‐phenylthiazoline‐4‐carboxylic acid: structure and catalytic activity for transfer hydrogenation reaction
inferred← citeshttps://doi.org/10.1002/aoc.3538openalex-snapshot
Transfer hydrogenation of aryl ketones with homogeneous ruthenium catalysts containing diazafluorene ligands
inferred← citeshttps://doi.org/10.1002/aoc.3919openalex-snapshot
Ferrocene based chiral binuclear η6‐benzene‐Ru(II)‐phosphinite complexes: Synthesis, characterization and catalytic activity in asymmetric reduction of ketones
inferred← citeshttps://doi.org/10.1002/aoc.5068openalex-snapshot
Some Novel Dinuclear phenylboronates of biologically potent β‐enaminoesters: Synthesis, Spectroscopic characterization, antimicrobial activity and their antiandrogenic effect
inferred← citeshttps://doi.org/10.1002/cctc.201300825openalex-snapshot
Expanding the Chemical Diversity in Artificial Imine Reductases Based on the Biotin–Streptavidin Technology
inferred← citeshttps://doi.org/10.1002/chem.200900548openalex-snapshot
Asymmetric Transfer Hydrogenation of Ketones Catalyzed by Amino Acid Derived Rhodium Complexes: On the Origin of Enantioselectivity and Enantioswitchability
inferred← citeshttps://doi.org/10.1002/chem.201102520openalex-snapshot
Double Stereodifferentiation in the Catalytic Asymmetric Aziridination of Imines Prepared from α‐Chiral Amines
inferred← citeshttps://doi.org/10.1002/ejic.200700267openalex-snapshot
(Arene)ruthenium(II) Complexes Containing Substituted Bis(pyrazolyl)methane Ligands – Catalytic Behaviour in Transfer Hydrogenation of Ketones
inferred← citeshttps://doi.org/10.1002/ejoc.201101164openalex-snapshot
Application of Proline‐Functionalised 1,2‐Diphenylethane‐1,2‐diamine (DPEN) in Asymmetric Transfer Hydrogenation of Ketones
inferred← citeshttps://doi.org/10.1002/mas.20309openalex-snapshot
Structural analysis of organometallic compounds with soft ionization mass spectrometry
inferred← citeshttps://doi.org/10.1002/slct.201702538openalex-snapshot
Ru(II)‐ η 6 ‐benzene Complexes of Dibenzosuberenyl Appended Aroyl/Acylthiourea Ligands: In vitro Biomolecular Interaction Studies and Catalytic Transfer Hydrogenation
inferred← citeshttps://doi.org/10.1007/s00775-011-0794-7openalex-snapshot
Synthesis and characterization of an unsymmetrical cobalt(III) active site analogue of nitrile hydratase
inferred← citeshttps://doi.org/10.1007/s10562-015-1680-7openalex-snapshot
Effect of NH Acidity on Transfer Hydrogenation of Noyori–Ikariya Catalyst
inferred← citeshttps://doi.org/10.1007/s10965-021-02454-9openalex-snapshot
Synthesis of Dowex functionalised half-sandwich Ru (II) (η6-p-cymene) complex as effective and selective hydrogenation of furfural to levulinic acid
inferred← citeshttps://doi.org/10.1007/s11172-012-0267-3openalex-snapshot
Pd-Catalyzed asymmetric transformations involving P*-mono- and P*,N-bidentate diamidophosphites derived from (2S,3S)-N 2,3-dimethyl-N 1-phenylpentane-1,2-diamine
inferred← citeshttps://doi.org/10.1007/s11243-021-00461-9openalex-snapshot
Half-sandwich ruthenium(II) complexes containing 4-substituted aniline derivatives: structural characterizations and catalytic properties in transfer hydrogenation of ketones
inferred← citeshttps://doi.org/10.1007/s11426-019-9606-2openalex-snapshot
Enantioselective three-component Ugi reaction catalyzed by chiral phosphoric acid
inferred← citeshttps://doi.org/10.1007/s13738-018-1569-7openalex-snapshot
Synthesis and electrochemical characterization of iminophosphine-based ruthenium(II) complexes and application in asymmetric transfer hydrogenation reaction as catalysts
inferred← citeshttps://doi.org/10.1016/j.apcata.2013.04.030openalex-snapshot
Polymer-supported chiral α-amino amides for the asymmetric addition of diethylzinc to aldehydes: Transforming an inactive homogeneous system into an efficient catalyst
inferred← citeshttps://doi.org/10.1016/j.apcata.2026.120769openalex-snapshot
Catalytic performance of Ru(0) nanoparticles supported on K-OMS-2 in transfer hydrogenation reactions
inferred← citeshttps://doi.org/10.1016/j.ccr.2007.12.016openalex-snapshot
NMR investigation of non-covalent aggregation of coordination compounds ranging from dimers and ion pairs up to nano-aggregates
inferred← citeshttps://doi.org/10.1016/j.ccr.2014.06.012openalex-snapshot
The application of electrospray ionization mass spectrometry to homogeneous catalysis
inferred← citeshttps://doi.org/10.1016/j.crci.2013.08.011openalex-snapshot
Screening of a library of hemisalen ligands in asymmetric H-transfer: Reduction of aromatic ketones in water
inferred← citeshttps://doi.org/10.1016/j.ica.2006.12.011openalex-snapshot
Tetracoordinate diamidato-bis(phosphanyl) metal systems: Synthesis, characterization, and electrochemical analysis of palladium(II) complexes
inferred← citeshttps://doi.org/10.1016/j.ica.2010.12.028openalex-snapshot
trans- and cis-Ru(II) aminophosphine complexes: Syntheses, X-ray structures and catalytic activity in transfer hydrogenation of acetophenone derivatives
inferred← citeshttps://doi.org/10.1016/j.ica.2010.12.056openalex-snapshot
Diamidato-bis(diphenylphosphino) platinum(II) complexes: Synthesis, characterization, and reactivity in the presence of acid
inferred← citeshttps://doi.org/10.1016/j.ica.2012.02.034openalex-snapshot
Synthesis and catalytic activity of ruthenium(II) complexes containing pyridine-based tridentate triamines ( ′NNN⌢⌢′ ) and pyridine carboxylate ligands ( NO⌢ )
inferred← citeshttps://doi.org/10.1016/j.ica.2012.12.005openalex-snapshot
Rhodium-catalyzed transfer hydrogenation with functionalized bis(phosphino)amine ligands
inferred← citeshttps://doi.org/10.1016/j.ica.2017.11.044openalex-snapshot
Chiral C2-symmetric η6-p-cymene-Ru(II)-phosphinite complexes: Synthesis and catalytic activity in asymmetric reduction of aromatic, methyl alkyl and alkyl/aryl ketones
inferred← citeshttps://doi.org/10.1016/j.ica.2022.120812openalex-snapshot
Preparation of catechol boronate esters enabled by N → B dative bond as efficient, stable, and green catalysts for the transfer hydrogenation of various ketones
inferred← citeshttps://doi.org/10.1016/j.inoche.2025.116066openalex-snapshot
Investigation of photocatalytic and catalytic activity of g-C3N4/TiO2 supported Ru(0) nanoparticles in transfer hydrogenation reaction of various ketones
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2014.03.004openalex-snapshot
Fluorine/phenyl chelated boron complexes: Synthesis, fluorescence properties and catalyst for transfer hydrogenation of aromatic ketones
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2006.07.036openalex-snapshot
Supramolecular chemistry of half-sandwich organometallic building blocks based on RuCl2(p-cymene)Ph2PCH2Y
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2008.04.027openalex-snapshot
Asymmetric transfer hydrogenation of ketones catalyzed by ruthenium(II) complexes bearing a chiral phosphinoferrocenyloxazoline ligand
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2009.04.015openalex-snapshot
New active ruthenium(II) complexes based N3,N3′-bis(diphenylphosphino)-2,2′-bipyridine-3,3′-diamine and P,P′-diphenylphosphinous acid-P,P′-[2,2′-bipyridine]-3,3′-diyl ester ligands for transfer hydrogenation of aromatic ketones by propan-2-ol
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2009.05.010openalex-snapshot
Diastereomeric half-sandwich Ru(II) cationic complexes containing amino amide ligands. Synthesis, solution properties, crystal structure and catalytic activity in transfer hydrogenation of acetophenone
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2009.06.008openalex-snapshot
Carbonyl rhodium(I) complexes containing (H)PNX (X = O or N) ligands deriving from natural aminoacid–amides. Synthesis, X-ray structure and spectroscopic characterization
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2010.07.030openalex-snapshot
Cationic and neutral ruthenium(II) complexes containing both arene or Cp* and functionalized aminophosphines. Application to hydrogenation of aromatic ketones
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2010.12.027openalex-snapshot
Asymmetric transfer hydrogenation of acetophenone derivatives with novel chiral phosphinite based η6-p-cymene/ruthenium(II) catalysts
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2012.07.009openalex-snapshot
1,8-Bis(dimethylamino)-2-(4-methoxyphenyl)naphthalene: An electrospray-active analogue for η6-coordinating ligands
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2012.08.031openalex-snapshot
Applications of transition metal complexes containing 3,3′-bis(diphenylphosphinoamine)-2,2′-bipyridine ligand to transfer hydrogenation of ketones
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2016.09.006openalex-snapshot
Transfer hydrogenation reaction using novel ionic liquid based Rh(I) and Ir(III)-phosphinite complexes as catalyst
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2020.121129openalex-snapshot
Synthesis, characterization and crystal structures of half-sandwich ruthenium complexes with bidentate chiral Schiff-base ligands
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2021.121765openalex-snapshot
Enantioselective reduction of prochiral ketones promoted by amino amide ruthenium complexes: A DFT study
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2023.122800openalex-snapshot
Synthesis of half-sandwich ruthenium(II) and iridium(III) complexes containing imidazole-based phosphinite ligands and their use in catalytic transfer hydrogenation of acetophenone with isopropanol
inferred← citeshttps://doi.org/10.1016/j.molcata.2010.04.010openalex-snapshot
Novel neutral phosphinite bridged dinuclear ruthenium(II) arene complexes and their catalytic use in transfer hydrogenation of aromatic ketones: X-ray structure of a new Schiff base, N3,N3′-di-2-hydroxybenzylidene-[2,2′]bipyridinyl-3,3′-diamine
inferred← citeshttps://doi.org/10.1016/j.poly.2009.12.035openalex-snapshot
Ruthenium-catalyzed transfer hydrogenation of aromatic ketones with aminophosphine or bis(phosphino)amine ligands derived from isopropyl substituted anilines
inferred← citeshttps://doi.org/10.1016/j.poly.2010.12.011openalex-snapshot
Ruthenium complexes of aminophosphine ligands and their use as pre-catalysts in the transfer hydrogenation of aromatic ketones: X-ray crystal structure of thiophene-2-(N-diphenylthiophosphino)methylamine
inferred← citeshttps://doi.org/10.1016/j.poly.2014.05.079openalex-snapshot
Ionic liquid based Ru(II)–phosphinite compounds and their catalytic use in transfer hydrogenation: X-ray structure of an ionic compound 1-chloro-3-(3-methylimidazolidin-1-yl)propan-2-ol
inferred← citeshttps://doi.org/10.1016/j.poly.2014.12.040openalex-snapshot
A new phosphazene derivative, spiro-N3P3[(O2C12H8)2(OC6H6N-3)2], and its Ru(II) complex: Syntheses, crystal structure, catalytic activity and antimicrobial activity studies
inferred← citeshttps://doi.org/10.1016/j.poly.2014.12.046openalex-snapshot
A ruthenium(II) bipyridine complex containing a 4,5-diazafluorene moiety: Synthesis, characterization and its applications in transfer hydrogenation of ketones and dye sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.saa.2015.01.094openalex-snapshot
Synthesis, spectroscopic and catalytic properties of some new boron hybrid molecule derivatives by BF2 and BPh2 chelation
inferred← citeshttps://doi.org/10.1016/j.tet.2012.11.025openalex-snapshot
C2 symmetrical nickel complexes derived from α-amino amides as efficient catalysts for the enantioselective addition of dialkylzinc reagents to aldehydes
inferred← citeshttps://doi.org/10.1016/j.tetasy.2010.04.002openalex-snapshot
A modular design of ruthenium(II) catalysts with chiral C2-symmetric phosphinite ligands for effective asymmetric transfer hydrogenation of aromatic ketones
inferred← citeshttps://doi.org/10.1016/j.tetasy.2013.02.010openalex-snapshot
Development of P∗-monodentate diamidophosphites with a C1-symmetric 1,2-diamine backbone: the effects of substituents in the 1,3,2-diazaphospholidine cycle on Pd-catalyzed asymmetric allylations
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.09.120openalex-snapshot
Enantioselective nickel-catalyzed conjugate addition of dialkylzinc to chalcones using chiral α-amino amides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.08.116openalex-snapshot
Fine-tuning catalytic activity and selectivity—[Rh(amino acid thioamide)] complexes for efficient ketone reduction
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.08.025openalex-snapshot
Visual chiral recognition of mandelic acid and α-amino acid derivatives by enantioselective gel formation and precipitation
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.6b01028openalex-snapshot
Troponate/Aminotroponate Ruthenium–Arene Complexes: Synthesis, Structure, and Ligand-Tuned Mechanistic Pathway for Direct C–H Bond Arylation with Aryl Chlorides in Water
inferred← citeshttps://doi.org/10.1021/acs.jpcc.9b04179openalex-snapshot
Indirect Detection of Short-Lived Hydride Intermediates of Iridium N-Heterocyclic Carbene Complexes via Chemical Exchange Saturation Transfer Spectroscopy
inferred← citeshttps://doi.org/10.1021/acscatal.6b00623openalex-snapshot
ESI-MS Insights into Acceptorless Dehydrogenative Coupling of Alcohols
inferred← citeshttps://doi.org/10.1021/ic201343wopenalex-snapshot
Synthesis, Reactivity Studies, Structural Aspects, and Solution Behavior of Half Sandwich Ruthenium(II)N,N′,N″-Triarylguanidinate Complexes
inferred← citeshttps://doi.org/10.1021/jo061154lopenalex-snapshot
The “Reverse-Tethered” Ruthenium (II) Catalyst for Asymmetric Transfer Hydrogenation: Further Applications
inferred← citeshttps://doi.org/10.1021/jo501273topenalex-snapshot
Ruthenium-Catalyzed N-Alkylation of Amines with Alcohols under Mild Conditions Using the Borrowing Hydrogen Methodology
inferred← citeshttps://doi.org/10.1021/jo802611topenalex-snapshot
Synthesis of a Fluorine-Substituted Puromycin Derivative for Brønsted Studies of Ribosomal-Catalyzed Peptide Bond Formation
inferred← citeshttps://doi.org/10.1021/ol062227qopenalex-snapshot
Enantioswitchable Catalysts for the Asymmetric Transfer Hydrogenation of Aryl Alkyl Ketones
inferred← citeshttps://doi.org/10.1021/om3001394openalex-snapshot
Half-Sandwich Complexes of Osmium(II) with l -α-Amino Carboxylate Ligands as Asymmetric Transfer Hydrogenation Catalysts. On the Origin of the Enantioselectivity
inferred← citeshttps://doi.org/10.1021/om4010548openalex-snapshot
Chiral (η6-p-Cymene)ruthenium(II) Complexes Containing Monodentate Acylthiourea Ligands for Efficient Asymmetric Transfer Hydrogenation of Ketones
inferred← citeshttps://doi.org/10.1021/om700775uopenalex-snapshot
From Ion Pairs to Ion Triples through a Hydrogen Bonding-Driven Aggregative Process
inferred← citeshttps://doi.org/10.1021/om8009969openalex-snapshot
Reactivity, Structures, and NMR Spectroscopy of Half-Sandwich Pentamethylcyclopentadienyl Rhodium Amido Complexes Relevant to Transfer Hydrogenation
inferred← citeshttps://doi.org/10.1021/om9001268openalex-snapshot
Base-Free Transfer Hydrogenation of Ketones Using Arene Ruthenium(II) Complexes
inferred← citeshttps://doi.org/10.1039/c0ob00400fopenalex-snapshot
Asymmetric transfer hydrogenation of ketones catalyzed by rhodium complexes containing amino acid triazole ligands
inferred← citeshttps://doi.org/10.1039/c3dt51275dopenalex-snapshot
Synthesis, characterisation and biological activities of [(p-cym)RuX(pz4lut)]n+ and [{(p-cym)RuX}2(μ-pz4lut)]n+ (X = Cl, H2O and pz4lut = α,α,α′,α′-tetra(pyrazol-1-yl)-2,6-lutidine)
inferred← citeshttps://doi.org/10.1039/c4ra15341copenalex-snapshot
Dual stereocontrolled alkylation of aldehydes with polystyrene-supported nickel complexes derived from α-amino amides
inferred← citeshttps://doi.org/10.1039/c6ob01878eopenalex-snapshot
Mechanistic implications of the enantioselective addition of alkylzinc reagents to aldehydes catalyzed by nickel complexes with α-amino amide ligands
inferred← citeshttps://doi.org/10.1039/c6ra12428copenalex-snapshot
Ru( ii )-p-cymene complexes containing esters of chiral d / l -phenylalanine derived aroylthiourea ligands for enantioselective reduction of pro-chiral ketones
inferred← citeshttps://doi.org/10.1039/c7ra04152gopenalex-snapshot
Syntheses, characterisation, and catalytic role of (η 5 -C 5 Me 5 )Rh( iii ) guanidinato complexes in transfer hydrogenation (TH) and TH–etherification
inferred← citeshttps://doi.org/10.1039/c9ra08736bopenalex-snapshot
Anticancer and antimicrobial properties of novel η 6 - p -cymene ruthenium( ii ) complexes containing a N,S-type ligand, their structural and theoretical characterization
inferred← citeshttps://doi.org/10.1080/00958972.2017.1300659openalex-snapshot
Developments in transfer hydrogenations of aromatic ketones catalyzed by boron compounds
inferred← citeshttps://doi.org/10.1080/00958972.2022.2054339openalex-snapshot
Ketone transfer hydrogenation reactions catalyzed by catalysts based on a phosphinite ligand
inferred← citeshttps://doi.org/10.1080/10426507.2014.966190openalex-snapshot
Synthesis of Tetranuclear Ruthenium (Ii) Complex of Pyridyloxy-Substituted 2,2′-Dioxybiphenyl-Cyclotriphosphazene Platform and its Catalytic Application in the Transfer Hydrogenation of Ketones
inferred← citeshttps://doi.org/10.1080/10426507.2021.1948852openalex-snapshot
Hg(II) and Ru(II) complexes of mono- and dichalcogenides of bis(diphenylphosphino)amine chelating ligands: Synthesis, characterization and catalytic activity in transfer hydrogenation of acetophenone derivatives
inferred← citeshttps://doi.org/10.1080/15533174.2012.751421openalex-snapshot
Synthesis and Catalytic Activity of Semiconducting p-Cymene Ruthenium 1,3,4-Thiadiazole and 1,2,4-Triazole Complexes
inferred← citeshttps://doi.org/10.1515/mgmc-2015-0023openalex-snapshot
Some heteroleptic boron derivatives and their isomers derived from Schiff bases and glycol: synthesis, characterization and antimicrobial activities
inferred← citeshttps://doi.org/10.2174/1876214x01003010030openalex-snapshot
Transfer Hydrogenation of Ketones Using Recyclable (η6-Arene) Ruthenium(II) Naphthylazo-p-Methyl Phenolate Complex~!2009-08-25~!2009-10-14~!2010-03-30~!
inferred← citeshttps://doi.org/10.3390/molecules25112501openalex-snapshot
An Efficient Greener Approach for N-acylation of Amines in Water Using Benzotriazole Chemistry
inferred← citeshttps://doi.org/10.3906/kim-1506-15openalex-snapshot
The role of N-heterocyclic carbene substituents on ruthenium(II) complexes in the catalytic transfer hydrogenation of acetophenone
inferred← citeshttps://doi.org/10.3987/com-09-11863openalex-snapshot
Synthesis of Optically Active γ-Valerolactone and γ-Nonanolactone via Optical Resolution Using Chiral Amine Derived from Amino Acid
inferred← citeshttps://doi.org/10.4236/mrc.2014.33010openalex-snapshot
The Nature of the True Catalyst in Transfer Hydrogenation with Alcohol Donors Using (arene)2Ru2Cl4(II)/TsDPEN Precursor
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.