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Large-Scale Carbonyl Reductions in the Pharmaceutical Industry
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inferredcites →https://doi.org/10.1002/(sici)1521-3773(19980817)37:15<1986::aid-anie1986>3.0.co;2-zopenalex-snapshot
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inferredcites →https://doi.org/10.1002/0470855800openalex-snapshot
Catalysts for Fine Chemical Synthesis
inferredcites →https://doi.org/10.1002/0470855800.ch10openalex-snapshot
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inferredcites →https://doi.org/10.1002/0470855800.ch11openalex-snapshot
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inferredcites →https://doi.org/10.1002/0470855800.ch9openalex-snapshot
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inferredcites →https://doi.org/10.1002/1521-3773(20010105)40:1<40::aid-anie40>3.0.co;2-5openalex-snapshot
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inferredcites →https://doi.org/10.1002/1615-4169(200108)343:6/7<527::aid-adsc527>3.0.co;2-iopenalex-snapshot
Enzymatic Synthesis of Chiral Intermediates for Drug Development
inferredcites →https://doi.org/10.1002/9780470054581openalex-snapshot
Encyclopedia of Industrial Biotechnology
inferredcites →https://doi.org/10.1002/adsc.200390000openalex-snapshot
Selective Hydrogenation for Fine Chemicals: Recent Trends and New Developments
inferredcites →https://doi.org/10.1002/anie.199406851openalex-snapshot
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inferredcites →https://doi.org/10.1002/anie.200806086openalex-snapshot
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inferredcites →https://doi.org/10.1002/aoc.1137openalex-snapshot
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inferredcites →https://doi.org/10.1002/chem.19960020312openalex-snapshot
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inferredcites →https://doi.org/10.1002/chir.10129openalex-snapshot
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inferredcites →https://doi.org/10.1002/cssc.201100134openalex-snapshot
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inferredcites →https://doi.org/10.1016/0022-328x(85)88019-0openalex-snapshot
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inferredcites →https://doi.org/10.1016/0926-860x(95)00097-6openalex-snapshot
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inferredcites →https://doi.org/10.1016/b978-0-08-052349-1.00230-4openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.tet.2004.09.027openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.tet.2006.05.036openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.tet.2008.04.072openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.tet.2009.09.054openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.tetasy.2003.07.024openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.tetasy.2003.08.043openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.tetasy.2008.12.035openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.tetlet.2005.12.067openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4020(00)00617-7openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4020(01)89692-7openalex-snapshot
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inferredcites →https://doi.org/10.1021/bk-1996-0645openalex-snapshot
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inferredcites →https://doi.org/10.1021/jo901267xopenalex-snapshot
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inferredcites →https://doi.org/10.1021/ol047925uopenalex-snapshot
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Hydride Reduction of a Lactate Ester: Optimisation and Scale-Up
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The Synthesis of a GH-Releasing Compound NNC 26-1089
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A New Route to Prepare 6-Chloro-5-(2-chloroethyl)oxindole
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Scale-Up Synthesis of the Dopamine Uptake Inhibitor GBR-12909
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A Practical Synthesis of the RARγ Agonist, BMS-270394
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Process Improvements for the Preparation of Kilo Quantities of a Series of Isoindoline Compounds
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The Development of a Large-Scale Synthesis of Matrix Metalloproteinase Inhibitor, ABT-518
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An Expedient Synthesis of 6α-Fluoroursodeoxycholic Acid
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Reaction Safety: A Critical Parameter in the Development of a Scaleable Synthesis of 2,3-Bis-chloromethylpyridine Hydrochloride
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Efficient Enantioselective Synthesis of the NMDA 2B Receptor Antagonist Ro 67-8867
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A Scalable Asymmetric Synthesis of (R)-2-Amino-1-(3-pyridinyl)ethanol Dihydrochloride via an Oxazaborolidine Catalyzed Borane Reduction
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Process Development and Scale-Up of the PPAR Agonist NNC 61-4655
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An Efficient and Cost-Effective Synthesis of Pagoclone
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Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 2: Synthesis of Fragments C1-6 and C9-14
inferredcites →https://doi.org/10.1021/op034132zopenalex-snapshot
Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 3: Synthesis of Fragment C15-21
inferredcites →https://doi.org/10.1021/op034133ropenalex-snapshot
Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 4: Preparation of Fragment C7-24
inferredcites →https://doi.org/10.1021/op034134jopenalex-snapshot
Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 5: Linkage of Fragments C1-6 and C7-24 and Finale
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Development of a Scaleable Synthesis of a 3-Aminopyrazinone Acetamide Thrombin Inhibitor
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Safety Notables: Information from the Literature
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An Improved Process for the Preparation of Trimethylhydrazine and Its Coupling with an Activated Acid Intermediate
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Development of an Efficient Process for the Preparation of Sch 39166: Aziridinium Chemistry on Scale
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Use of DOE for Rapid Development of a Red-Al Reduction Process for the Synthesis of 3,4-Isopropylidenedioxypyrrolidine Hydrotosylate
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First Scale-Up: Problems and Resolutions on the Synthesis of WAY-253752, a Novel, Dual-Acting SSRI/5HT1A Antagonist
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1002/anie.202406588openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cctc.201701287openalex-snapshot
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Efficient Base‐Catalyzed Hydrosilylation of Tertiary Amides to Aldehydes
inferred← citeshttps://doi.org/10.1002/cctc.202300004openalex-snapshot
Promising Catalytic Application by Pincer Metal Complexes: Recent Advances in Hydrogenation of Carbon‐Based Molecules
inferred← citeshttps://doi.org/10.1002/cctc.202301417openalex-snapshot
Aldehyde and Ketone Hydroboration Mediated by a Heterogeneous Single‐Site Molybdenum‐Dioxo Catalyst: Scope and Mechanistic Implications
inferred← citeshttps://doi.org/10.1002/cctc.202401237openalex-snapshot
Concentration‐Dependent Thermodynamics of the Inhibitory Paths in Homogeneous Mn(I) Hydrogenation Catalysis
inferred← citeshttps://doi.org/10.1002/cctc.202401986openalex-snapshot
Iron‐Salen Complexes for Hydroboration of Ketones: Enhancing Reactivity via Ligand Modulation at the Phenylene Bridge
inferred← citeshttps://doi.org/10.1002/cctc.202500206openalex-snapshot
Recent Trends and Mechanistic Insights in the Catalytic Hydroboration of Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/celc.202100617openalex-snapshot
Molecular Electrocatalytic Hydrogenation of Carbonyls and Dehydrogenation of Alcohols
inferred← citeshttps://doi.org/10.1002/chem.201202857openalex-snapshot
Reductive Cleavage of Amides to Alcohols and Amines Catalyzed by Well‐Defined Bimetallic Molybdenum Complexes
inferred← citeshttps://doi.org/10.1002/chem.201302728openalex-snapshot
Base‐Catalyzed Hydrosilylation of Ketones and Esters and Insight into the Mechanism
inferred← citeshttps://doi.org/10.1002/chem.201403497openalex-snapshot
Cesium Carbonate Catalyzed Chemoselective Hydrosilylation of Aldehydes and Ketones under Solvent‐Free Conditions
inferred← citeshttps://doi.org/10.1002/chem.201604762openalex-snapshot
TiO2‐Supported Re as a General and Chemoselective Heterogeneous Catalyst for Hydrogenation of Carboxylic Acids to Alcohols
inferred← citeshttps://doi.org/10.1002/chem.202003862openalex-snapshot
Insights into LiAlH4 Catalyzed Imine Hydrogenation
inferred← citeshttps://doi.org/10.1002/chem.202201000openalex-snapshot
An Expedient Method for the Umpolung Coupling of Enols with Heteronucleophiles**
inferred← citeshttps://doi.org/10.1002/chem.202201722openalex-snapshot
Terpyridine Diphosphine Ruthenium Complexes as Efficient Photocatalysts for the Transfer Hydrogenation of Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/chem.202203023openalex-snapshot
Aluminium‐Catalyzed Selective Hydroboration of Esters and Epoxides to Alcohols: C−O Bond Activation
inferred← citeshttps://doi.org/10.1002/chem.202403449openalex-snapshot
Ce[N(SiMe3)2]3(THF)3‐Catalyzed Hydroboration of CO2, Esters and Epoxides with Pinacolborane: Selective Synthesis of Methanol in Multigram Scale
inferred← citeshttps://doi.org/10.1002/chem.202501218openalex-snapshot
An Asymmetric Reductive Amination Synthesis of Ritlecitinib Using (S)‐α‐Methylbenzylamine as Chiral Auxiliary
inferred← citeshttps://doi.org/10.1002/chem.202501396openalex-snapshot
Stannylenes Bearing an Amino‐Linked NHC Ligand as Efficient Catalysts for Hydroboration of Carbonyls and Imines
inferred← citeshttps://doi.org/10.1002/chir.23559openalex-snapshot
A concise review on recent advances in catalytic asymmetric hydrogenation
inferred← citeshttps://doi.org/10.1002/chir.23660openalex-snapshot
Biocatalytic enantioselective synthesis of cenobamate, an antiepileptic drug
inferred← citeshttps://doi.org/10.1002/cite.202300155openalex-snapshot
Effect of Electrolyte Composition and Mass Transport on Electrochemical Hydrogenations of a Terminal Alkynol
inferred← citeshttps://doi.org/10.1002/cjoc.201900344openalex-snapshot
La[N(SiMe 3 ) 2 ] 3 ‐Catalyzed Hydroboration of Esters and Other Challenging Unsaturated Groups
inferred← citeshttps://doi.org/10.1002/cjoc.202100508openalex-snapshot
Tunable System for Electrochemical Reduction of Ketones and Phthalimides
inferred← citeshttps://doi.org/10.1002/cjoc.202200176openalex-snapshot
A Uranium( IV ) Alkyl Complex: Synthesis and Catalytic Property in Carbonyl Hydroboration
inferred← citeshttps://doi.org/10.1002/cphc.202400690openalex-snapshot
Quantifying Kinetically Relevant Species on Zr‐SiO2 Materials for MPV Reduction
inferred← citeshttps://doi.org/10.1002/cssc.201903459openalex-snapshot
Continuous‐Flow Amide and Ester Reductions Using Neat Borane Dimethylsulfide Complex
inferred← citeshttps://doi.org/10.1002/ejic.202000092openalex-snapshot
Nickel(II) Catalyzed Hydroboration: A Route to Selective Reduction of Aldehydes and N‐Allylimines
inferred← citeshttps://doi.org/10.1002/ejic.202000310openalex-snapshot
Palladium‐Catalyzed Selective Reduction of Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/ejic.202101030openalex-snapshot
Organoaluminum Cation Catalyzed Selective Hydrosilylation of Carbonyls, Alkenes, and Alkynes
inferred← citeshttps://doi.org/10.1002/ejoc.201300506openalex-snapshot
Biphasic Glycerol/2‐MeTHF, Ruthenium‐Catalysed Enantioselective Transfer Hydrogenation of Ketones Using Sodium Hypophosphite as Hydrogen Donor
inferred← citeshttps://doi.org/10.1002/ejoc.201601256openalex-snapshot
1‐Hydrosilatrane: A Locomotive for Efficient Ketone Reductions
inferred← citeshttps://doi.org/10.1002/ejoc.201700030openalex-snapshot
Direct Regioselective Alkylation of Non‐Basic Heterocycles with Alcohols and Cyclic Ethers through a Dehydrogenative Cross‐Coupling Reaction under Metal‐Free Conditions
inferred← citeshttps://doi.org/10.1002/ejoc.201700374openalex-snapshot
A Mild and Chemoselective Hydrosilylation of α‐Keto Amides by Using a Cs 2 CO 3 /PMHS/2‐MeTHF System
inferred← citeshttps://doi.org/10.1002/ejoc.201800544openalex-snapshot
Lewis Base Catalyzed Intramolecular Reduction of Salicylaldehydes by Pinacol‐Derived Chlorohydrosilane
inferred← citeshttps://doi.org/10.1002/ejoc.202100394openalex-snapshot
The Development of Organocatalytic Asymmetric Reduction of Carbonyls and Imines Using Silicon Hydrides
inferred← citeshttps://doi.org/10.1002/ejoc.202200539openalex-snapshot
Catalytic Isomerization of Unprotected Mesoionic N‐Heterocyclic Olefins and Their Lewis Adducts
inferred← citeshttps://doi.org/10.1002/ejoc.202300674openalex-snapshot
Catalytic Hydrosilylation of Imines by Aluminum Hydride Cations
inferred← citeshttps://doi.org/10.1002/ejoc.202300904openalex-snapshot
Exhaustive Reduction of Esters, Carboxylic Acids and Carbamates to Methyl Groups Catalyzed by Boronic Acids
inferred← citeshttps://doi.org/10.1002/ejoc.70666openalex-snapshot
Visible‐Light‐Driven Titanium‐Catalyzed Decarboxylative Oxidation of Carboxylic Acids and Amino Acid Derivatives
inferred← citeshttps://doi.org/10.1002/hlca.201800049openalex-snapshot
Reduction of N , N ‐Dimethylcarboxamides to Aldehydes by Sodium Hydride–Iodide Composite
inferred← citeshttps://doi.org/10.1002/hlca.201800144openalex-snapshot
Hydrogenation towards Synthetic Sandalwood Odorants in Fragrance Industry
inferred← citeshttps://doi.org/10.1002/hlca.201900166openalex-snapshot
Mechanistic Insights on Reduction of Carboxamides by Diisobutylaluminum Hydride and Sodium Hydride−Iodide Composite
inferred← citeshttps://doi.org/10.1002/slct.202101775openalex-snapshot
Phosphine‐Free Ruthenium Complex for Hydrogenation of Carbonyl Compounds: Synthesis and Applications
inferred← citeshttps://doi.org/10.1002/slct.202202679openalex-snapshot
Advances in Carbon‐Carbon Bond Activation by Using Photocatalysts: A Mini Review
inferred← citeshttps://doi.org/10.1002/slct.202302508openalex-snapshot
Green Hydrogenation of C=C, C=O, and C=N Bonds in Water by Palladium‐Tin Bimetallic Nanoparticles
inferred← citeshttps://doi.org/10.1002/slct.202304047openalex-snapshot
Valorization of Lignocellulosic Molecules through Homogeneous Ru‐Catalyzed C−C and C−N Bond Forming Reactions
inferred← citeshttps://doi.org/10.1002/slct.202304105openalex-snapshot
Hydrodeoxygenation of Carbonyl Compounds Biomass Derivatives Using CaH 2 over Pd/C
inferred← citeshttps://doi.org/10.1002/slct.202405725openalex-snapshot
Organocatalyzed α‐Deuteration of Ketones and Bioactive Carbonyl Compounds Using D 2 O as Deuterium Source
inferred← citeshttps://doi.org/10.1002/slct.202502707openalex-snapshot
Persulfate‐Mediated Facile Oxidation of Aromatic/Aliphatic Aldehyde to Carboxylic Acid
inferred← citeshttps://doi.org/10.1002/tcr.202100062openalex-snapshot
Application of Ketoreductase in Asymmetric Synthesis of Pharmaceuticals and Bioactive Molecules: An Update (2018–2020)
inferred← citeshttps://doi.org/10.1002/tcr.202200192openalex-snapshot
Metal/Non‐Metal Catalyzed Activation of Organic Nitriles
inferred← citeshttps://doi.org/10.1007/10_2014_291openalex-snapshot
Efficient Biocatalytic Synthesis of Chiral Chemicals
inferred← citeshttps://doi.org/10.1007/s00706-018-2279-7openalex-snapshot
Chemoselective transfer hydrogenation of aldehydes in aqueous media catalyzed by a well-defined iron(II) hydride complex
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/s11426-022-1501-yopenalex-snapshot
Iridium and B(C6F5)3 co-catalyzed chemoselective deoxygenative reduction of tertiary amides: application to the efficient synthesis and late-stage modification of pharmaceuticals
inferred← citeshttps://doi.org/10.1007/s12039-018-1579-0openalex-snapshot
Nano-sized Silicalite-1: novel route of synthesis, metal impregnation and its application in selective oxidation of toluene
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00813-2openalex-snapshot
8.11 Reduction of Carboxylic Acids and their Derivatives to Aldehydes
inferred← citeshttps://doi.org/10.1016/b978-0-08-102688-5.00032-5openalex-snapshot
Low-Coordinate Chemistry of Manganese and Iron
inferred← citeshttps://doi.org/10.1016/b978-0-12-820206-7.00142-6openalex-snapshot
Ruthenium and Osmium Complexes Containing NHC and π-Acid Ligands
inferred← citeshttps://doi.org/10.1016/b978-0-32-390644-9.00046-9openalex-snapshot
Industrial Applications of Asymmetric Synthesis in a Medicinal Chemistry Setting
inferred← citeshttps://doi.org/10.1016/b978-0-323-95893-6.00001-3openalex-snapshot
Visible light–driven organic synthesis under Rose Bengal photocatalysis
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00161-7openalex-snapshot
Reduction of Carboxylic Acids and Their Derivatives to Aldehydes
inferred← citeshttps://doi.org/10.1016/b978-0-443-15656-4.00003-3openalex-snapshot
A general overview on hydrogenation catalytic systems
inferred← citeshttps://doi.org/10.1016/bs.acat.2021.08.005openalex-snapshot
Asymmetric hydrogenation in industry
inferred← citeshttps://doi.org/10.1016/j.apcata.2021.118230openalex-snapshot
Stable Ni catalyst encapsulated in N-doped carbon nanotubes for one-pot reductive amination of nitroarenes with aldehydes
inferred← citeshttps://doi.org/10.1016/j.apcata.2026.121017openalex-snapshot
Developing Fe-Ni-B nanosheet catalyst for selective hydrogenation of aromatic aldehydes and solvent-free single-step reductive amination
inferred← citeshttps://doi.org/10.1016/j.apmt.2024.102200openalex-snapshot
iADOR yields diverse shape-selective solid Lewis acid catalysts
inferred← citeshttps://doi.org/10.1016/j.apmt.2024.102208openalex-snapshot
One-pot synthesis of multivariate porphyrinic metal-organic frameworks with the insertion of metallobipyridine and the cooperative catalysis for carbonyl hydrosilylation
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.104651openalex-snapshot
Scope and limitations of biocatalytic carbonyl reduction with white-rot fungi
inferred← citeshttps://doi.org/10.1016/j.catcom.2018.04.014openalex-snapshot
Lanthanide aryloxides catalyzed hydroboration of aldehydes and ketones
inferred← citeshttps://doi.org/10.1016/j.catcom.2018.10.030openalex-snapshot
Highly enantioselective reduction of ketones in air catalyzed by Rh-based macrocycles
inferred← citeshttps://doi.org/10.1016/j.cattod.2026.115782openalex-snapshot
Alkali cations enhance Zr-beta zeolite selectivity in citronellal Meerwein-Ponndorf-Verley reduction
inferred← citeshttps://doi.org/10.1016/j.cclet.2020.09.011openalex-snapshot
Cobalt-catalyzed asymmetric hydrogenation of ketones: A remarkable additive effect on enantioselectivity
inferred← citeshttps://doi.org/10.1016/j.ccr.2015.01.008openalex-snapshot
Iron-catalyzed reduction of carboxylic and carbonic acid derivatives
inferred← citeshttps://doi.org/10.1016/j.ccr.2015.04.007openalex-snapshot
Ruthenium and osmium complexes containing 2-(aminomethyl)pyridine (Ampy)-based ligands in catalysis
inferred← citeshttps://doi.org/10.1016/j.ccr.2018.06.005openalex-snapshot
Current advances on ruthenium(II) N-heterocyclic carbenes in hydrogenation reactions
inferred← citeshttps://doi.org/10.1016/j.ccr.2025.216438openalex-snapshot
An overview on copper in industrial chemistry: From ancient pigment to modern catalysis
inferred← citeshttps://doi.org/10.1016/j.chempr.2017.06.001openalex-snapshot
Electrostatic Catalyst Generated from Diazadiborinine for Carbonyl Reduction
inferred← citeshttps://doi.org/10.1016/j.gee.2026.02.003openalex-snapshot
Syngas-promoted selective catalytic hydrogenolysis of cellulose into C6-ketones
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e32550openalex-snapshot
Influence of deep eutectic solvents on redox biocatalysis involving alcohol dehydrogenases
inferred← citeshttps://doi.org/10.1016/j.ica.2020.120096openalex-snapshot
Synthesis of new rhodium(III) complex by benzylic C S bond cleavage of thioether containing NNS donor Schiff base ligand: Investigation of catalytic activity towards transfer hydrogenation of ketones
inferred← citeshttps://doi.org/10.1016/j.jcat.2018.04.018openalex-snapshot
Computational insights into the catalytic role of the base promoters in ester hydrogenation with homogeneous non-pincer-based Mn-P,N catalyst
inferred← citeshttps://doi.org/10.1016/j.jcat.2021.04.023openalex-snapshot
Ambient-pressure highly active hydrogenation of ketones and aldehydes catalyzed by a metal-ligand bifunctional iridium catalyst under base-free conditions in water
inferred← citeshttps://doi.org/10.1016/j.jcat.2022.12.012openalex-snapshot
Decoration of Ru nanoparticles with mononuclear MoOx boosts the hydrodeoxygenation of amides to amines
inferred← citeshttps://doi.org/10.1016/j.jcat.2023.01.008openalex-snapshot
Asymmetric transfer hydrogenation of ketones catalyzed by chiral macrocyclic cobalt(II) complexes
inferred← citeshttps://doi.org/10.1016/j.jcat.2023.04.012openalex-snapshot
Manganese-catalyzed deoxygenation of secondary and tertiary amides under mild conditions
inferred← citeshttps://doi.org/10.1016/j.jcat.2023.06.035openalex-snapshot
General and selective homogeneous Ru-catalyzed transfer hydrogenation, deuteration, and methylation of functional compounds using methanol
inferred← citeshttps://doi.org/10.1016/j.jcat.2024.115664openalex-snapshot
Mechanistic investigation and machine learning exploration of structure-activity relationship of NHC-Mn catalyzed ester hydrosilylation reaction
inferred← citeshttps://doi.org/10.1016/j.jcat.2025.116034openalex-snapshot
Exhaustive reduction of aromatic esters and carboxylic acids with a homogeneous cobalt catalyst
inferred← citeshttps://doi.org/10.1016/j.jcat.2025.116495openalex-snapshot
Aldehydes as reducing agents: Reductive alkylation of ketones
inferred← citeshttps://doi.org/10.1016/j.jcat.2026.116889openalex-snapshot
A highly efficient iridium catalyst for ketone asymmetric hydrogenation with exceptional turnover number
inferred← citeshttps://doi.org/10.1016/j.jcoa.2022.100063openalex-snapshot
Methyl acetoacetate derivatisation for improving liquid chromatography analysis of short chain aldehydes and water sensitive and chiral aldehydes
inferred← citeshttps://doi.org/10.1016/j.jiec.2016.08.015openalex-snapshot
Deoxygenative silylation of aromatic carbonyl compounds with HSiCl 3 in the presence of quaternary phosphonium chloride: A facile route to arylmethyltrichlorosilane
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2017.06.020openalex-snapshot
Osmium-hydride-carbonyl complex with thioether containing Schiff base ligand: Synthesis, crystal structure, electrochemistry and catalytic transfer hydrogenation
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2021.121972openalex-snapshot
Reactivity of aluminum hydrides supported with sterically hindered acenaphthene-1,2-diimines towards CO2
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2022.122288openalex-snapshot
Chemoselective hydrosilylation of carboxylic acids using a phosphine-free ruthenium complex and phenylsilane
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.jorganchem.2024.123325openalex-snapshot
New metallophthalocyanine (M: Ni(II) and Fe(II)) complexes as efficient catalysts for transfer hydrogenation of various ketones
inferred← citeshttps://doi.org/10.1016/j.matchemphys.2021.124309openalex-snapshot
Synthesis and characterization of highly dispersed cobaltous silicate as a catalyst for selective oxidation of toluene to benzaldehyde
inferred← citeshttps://doi.org/10.1016/j.mcat.2023.113626openalex-snapshot
A study on the oxidation of toluene to benzaldehyde by air catalyzed by polyoxometalate loaded on activated carbon
inferred← citeshttps://doi.org/10.1016/j.mcat.2024.114337openalex-snapshot
Light-enhancing ketone transfer hydrogenation catalyzed by diphosphine phenanthroline ruthenium complexes
inferred← citeshttps://doi.org/10.1016/j.mcat.2024.114516openalex-snapshot
2,6-Bis(pyrazol-1-yl)pyridine cobalt-catalyzed high selective hydroboration of alkenes
inferred← citeshttps://doi.org/10.1016/j.molcatb.2013.08.003openalex-snapshot
Synthesis of (R)-bambuterol based on asymmetric reduction of 1-[3,5-bis(dimethylcarbamoyloxy)phenyl]-2-chloroethanone with incubated whole cells of Williopsis californica JCM 3600
inferred← citeshttps://doi.org/10.1016/j.molcatb.2015.03.010openalex-snapshot
Biocatalysed reduction of carboxylic acids to primary alcohols in aqueous medium: A novel synthetic capability of the zygomycete fungus Syncephalastrum racemosum
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.140256openalex-snapshot
Shining light on green chemistry: BODIPY-infused porphyrin nanocomposite-enzymatic photocatalyst boosts selective aldehydes hydrogenation and organic transformation under solar spectrum
inferred← citeshttps://doi.org/10.1016/j.poly.2017.04.019openalex-snapshot
Synthesis and characterization of a ruthenium complex with bis(diphenylphosphino)propane and thioether containing ONS donor ligand: Application in transfer hydrogenation of ketones
inferred← citeshttps://doi.org/10.1016/j.poly.2022.116075openalex-snapshot
New palladium(II) complexes with ferrocenyl Schiff bases in the hydrogenation of aromatic ketones
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/10.1016/j.scp.2023.101309openalex-snapshot
Light-induced reduction of aryl ketones and aldehydes via Meerwein-Ponndorf-Verley-type reaction with isopropanol under Mild reaction conditions
inferred← citeshttps://doi.org/10.1016/j.supflu.2012.05.012openalex-snapshot
Transformations of acetophenone and its derivatives in supercritical fluid isopropanol/CO2 in a continuous flow reactor in the presence of alumina
inferred← citeshttps://doi.org/10.1016/j.surfin.2022.102601openalex-snapshot
Constructing a built-in electric field in monolayer g-C3N4 by carbon and oxygen co-doping for enhanced photocatalytic oxidation of toluene to benzaldehyde activity
inferred← citeshttps://doi.org/10.1016/j.tet.2018.06.048openalex-snapshot
Chemoselective reduction of aldehydes and ketones by potassium diisobutyl-t-butoxy aluminum hydride (PDBBA)
inferred← citeshttps://doi.org/10.1016/j.tet.2019.07.021openalex-snapshot
Ambient-pressure hydrogenation of ketones and aldehydes by a metal-ligand bifunctional catalyst [Cp*Ir(2,2′-bpyO)(H2O)] without using base
inferred← citeshttps://doi.org/10.1016/j.tet.2020.131639openalex-snapshot
Palladium-catalyzed external-CO-free reductive carbonylation of aryl sulfonates
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