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Reductive Amination of Aldehydes and Ketones with Sodium Triacetoxyborohydride. Studies on Direct and Indirect Reductive Amination Procedures 1
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Encyclopedia of Reagents for Organic Synthesis
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Basenbildung aus Carbonylverbindungen
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Synthesis and conformational analysis of isomeric 3‐propananilidotropanes
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In vitro inhibition of animal and higher plants 2,3-oxidosqualene-sterol cyclases by 2-aza-2,3- dihydrosqualene and derivatives, and by other ammonium-containing molecules
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Titanium(IV) isopropoxide and sodium borohydride : A reagent of choice for reductive amination
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Synthesis and biological activity of azasqualenes, bis-azasqualenes and derivatives
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REDUCTIVE ALKYLATION OF ANILINE WITH 2–INDANONE AND 2–TETRALONE
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Catalytic Hydrogenation Over Platinum Metals
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Catalysis in Organic Syntheses
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Observations relevant to the mechanism of the reductive aminations of ketones with sodium cyanoborohydride and ammonium acetate
inferredcites →https://doi.org/10.1016/s0040-4039(00)81383-0openalex-snapshot
Recent studies on veratrum alkaloids: a new reaction of sodium triacetoxyborohydride [NaBH(OAc)3]
inferredcites →https://doi.org/10.1016/s0040-4039(00)88322-7openalex-snapshot
Chemoselective reduction of aldehydes with tetra--butylammonium triacetoxyborohydride
inferredcites →https://doi.org/10.1016/s0040-4039(00)97905-xopenalex-snapshot
Reductive amination of aldehydes and ketones by using sodium triacetoxyborohydride
inferredcites →https://doi.org/10.1016/s0040-4039(01)81928-6openalex-snapshot
A general, highly stereoselective synthesis of amines
inferredcites →https://doi.org/10.1016/s0957-4166(00)82370-8openalex-snapshot
Magnesium ion mediated stereospecific formation of N-substituted ethanolamines during reductive amination
inferredcites →https://doi.org/10.1021/ja00741a013openalex-snapshot
Cyanohydridoborate anion as a selective reducing agent
inferredcites →https://doi.org/10.1021/ja00832a035openalex-snapshot
Reactions of sodium borohydride in acidic media. I. Reduction of indoles and alkylation of aromatic amines with carboxylic acids
inferredcites →https://doi.org/10.1021/ja01042a078openalex-snapshot
Lithium cyanohydridoborate, a versatile new reagent
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A Redetermination and Extension of the H0 Scale of Acidity in Aqueous Perchloric Acid
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Kinetics of the Catalytic Hydrogenation of Certain Schiff Bases1
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Secondary and Tertiary Amines from Nitro Compounds
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Secondary and Tertiary Amines from Azo Compounds
inferredcites →https://doi.org/10.1021/jo01053a501openalex-snapshot
N-Alkylation of Amides. A Novel Procedure
inferredcites →https://doi.org/10.1039/c39750000535openalex-snapshot
Reactions of sodium borohydride in acidic media. Selective reduction of aldehydes with sodium triacetoxyborohydride
inferredcites →https://doi.org/10.1039/p19840000717openalex-snapshot
Reductive aminations of ketones and aldehydes using borane–pyridine
inferredcites →https://doi.org/10.1055/s-1975-23685openalex-snapshot
Sodium Cyanoborohydride - A Highly Selective Reducing Agent for Organic Functional Groups
inferredcites →https://doi.org/10.1055/s-1987-28148openalex-snapshot
Reductive Amination of Ketones and Aldehydes at the Mercury-Cathode
inferredcites →https://doi.org/10.1055/s-1991-26642openalex-snapshot
A Simple Method for Preparation of Secondary Aromatic Amines
inferredcites →https://doi.org/10.1070/rc1980v049n01abeh002442openalex-snapshot
Catalytic Amination of Alcohols, Aldehydes, and Ketones
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CYANOBOROHYDRIDE. UTILITY AND APPLICATIONS IN ORGANIC SYNTHESIS. A REVIEW
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SODIUM BOROHYDRIDE IN CARBOXYLIC ACID MEDIA. A REVIEW OF THE SYNTHETIC UTILITY OF ACYLOXYBOROHYDRIDES
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Reductive Amination of Piperidines with Aldehydes Using Borane-Pyridine
inferredcites →https://doi.org/10.1080/00397919308011255openalex-snapshot
Borohydride Exchange Resin, a New Reducing Agent for Reductive Amination
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inferred← citeshttps://doi.org/10.1002/asia.201800575openalex-snapshot
A General Palladium–Phosphine Complex To Explore Aryl Tosylates in the N‐Arylation of Amines: Scope and Limitations
inferred← citeshttps://doi.org/10.1002/asia.202201241openalex-snapshot
Cationic Rhodium(I)‐Catalyzed Asymmetric Cyclohydroformylation of 1,6‐Enynes with Formaldehyde
inferred← citeshttps://doi.org/10.1002/asia.202300661openalex-snapshot
Easy Access to Tertiary Amines from Carbonyl Compounds with Substituted Amine‐Boranes: A Substrate, Catalyst, and Additive‐Free Approach Under Mild Conditions
inferred← citeshttps://doi.org/10.1002/asia.202401070openalex-snapshot
Insight into the Metal‐Free Reduction of Isocyanates to N‐Methyl Anilines at Room Temperature
inferred← citeshttps://doi.org/10.1002/bio.4339openalex-snapshot
Investigating the spectral and electrochemical properties of novel flavin‐pyrene dyads separated via variable spacer
inferred← citeshttps://doi.org/10.1002/bit.28604openalex-snapshot
Reductive amination cascades in cell‐free and resting whole cell formats for valorization of lignin deconstruction products
inferred← citeshttps://doi.org/10.1002/bkcs.10342openalex-snapshot
Yb( OTf )3‐catalyzed One‐Pot Three Component Synthesis for Tertiary Amines
inferred← citeshttps://doi.org/10.1002/bkcs.11012openalex-snapshot
Synthesis and Biological Evaluation of Substituted Pyrazole Constrained Piperazine Derivative Library for Dopamine Receptor Antagonist
inferred← citeshttps://doi.org/10.1002/bkcs.11424openalex-snapshot
Isothiouronium Salts as Catalysts for the Direct Reductive Amination of Aldehydes with a Hantzsch Ester
inferred← citeshttps://doi.org/10.1002/bkcs.11863openalex-snapshot
Direct Reductive Amination of Aldehydes Using Hantzsch Ester Promoted by N,N′‐Diphenyl‐S‐Benzylisothiouronium Iodide as an Organocatalyst
inferred← citeshttps://doi.org/10.1002/cbdv.202100530openalex-snapshot
Synthesis and Aldose Reductase Inhibition Effects of Novel N‐Benzyl‐4‐Methoxyaniline Derivatives
inferred← citeshttps://doi.org/10.1002/cbdv.202400471openalex-snapshot
Design, Synthesis and Biological Evaluation of Novel Gypsogenin Derivatives as Potential Anticancer and Antimicrobial Agents
inferred← citeshttps://doi.org/10.1002/cbdv.202401010openalex-snapshot
Synthesis, Evaluation and Docking Studies of Disubstituted N‐Heterocyclic Derivatives as Anticancer Agents
inferred← citeshttps://doi.org/10.1002/cbic.201200079openalex-snapshot
Novel (Phenylethynyl)pyrene–LNA Constructs for Fluorescence SNP Sensing in Polymorphic Nucleic Acid Targets
inferred← citeshttps://doi.org/10.1002/cbic.202000132openalex-snapshot
The in Vitro Antiplasmodial and Antiproliferative Activity of New Ferrocene‐Based α‐Aminocresols Targeting Hemozoin Inhibition and DNA Interaction
inferred← citeshttps://doi.org/10.1002/cbic.202400620openalex-snapshot
A Photo‐Caged Cross‐Linker for Identifying Protein‐Protein Interactions
inferred← citeshttps://doi.org/10.1002/cctc.201000046openalex-snapshot
Amination of Aliphatic Alcohols and Diols with an Iridium Pincer Catalyst
inferred← citeshttps://doi.org/10.1002/cctc.201100197openalex-snapshot
Highly Efficient and Selective Catalytic N‐Alkylation of Amines with Alcohols in Water
inferred← citeshttps://doi.org/10.1002/cctc.201200213openalex-snapshot
Reductive Amination of Ketones or Amination of Alcohols over Heterogeneous Cu Catalysts: Matching the Catalyst Support with the N‐Alkylating Agent
inferred← citeshttps://doi.org/10.1002/cctc.201200764openalex-snapshot
Fe‐Catalyzed Olefin Epoxidation with Tridentate Non‐Heme Ligands and Hydrogen Peroxide as the Oxidant
inferred← citeshttps://doi.org/10.1002/cctc.201300338openalex-snapshot
Nickel‐Catalysed Reductive Amination with Hydrosilanes
inferred← citeshttps://doi.org/10.1002/cctc.201402527openalex-snapshot
Synthesis of Amines by Reductive Amination of Aldehydes and Ketones using Co3O4/NGr@C Catalyst
inferred← citeshttps://doi.org/10.1002/cctc.201500764openalex-snapshot
Imine Reductase‐Catalyzed Intermolecular Reductive Amination of Aldehydes and Ketones
inferred← citeshttps://doi.org/10.1002/cctc.201801525openalex-snapshot
C‐N Bond Formation Catalyzed by Ruthenium Nanoparticles Supported on N‐Doped Carbon via Acceptorless Dehydrogenation to Secondary Amines, Imines, Benzimidazoles and Quinoxalines
inferred← citeshttps://doi.org/10.1002/cctc.201900335openalex-snapshot
Morphology‐Tuned Activity of Ru/Nb2O5 Catalysts for Ketone Reductive Amination
inferred← citeshttps://doi.org/10.1002/cctc.202101270openalex-snapshot
Elucidating the Role of Rh/C on the Pathways and Kinetics of Ketone‐to‐Secondary Amines Reaction
inferred← citeshttps://doi.org/10.1002/cctc.202500251openalex-snapshot
C‐Scorpionate Gold(III) Catalysts in Nitroarene Reduction: A Novel Strategy
inferred← citeshttps://doi.org/10.1002/cctc.202500989openalex-snapshot
Selective Ammonium Carbamate Crystallization: An Innovative Approach for Catalyst Recycling in Homogeneously Catalyzed Primary Amine Synthesis
inferred← citeshttps://doi.org/10.1002/ceat.200500030openalex-snapshot
A Kinetic Study on the Catalytic Reductive Methylation of Acetylhydrazine
inferred← citeshttps://doi.org/10.1002/ceur.202500094openalex-snapshot
Selective N‐Alkylation of Unprotected Amino Sugars by Alcohols. Application to the Synthesis of Sugar‐Based Surfactants
inferred← citeshttps://doi.org/10.1002/chem.200390007openalex-snapshot
Could Redox‐Switched Binding of a Redox‐Active Ligand to a Copper( II ) Centre Drive a Conformational Proton Pump Gate? A Synthetic Model Study
inferred← citeshttps://doi.org/10.1002/chem.200500551openalex-snapshot
Supramolecular Assembly of an Amphiphilic GdIII Chelate: Tuning the Reorientational Correlation Time and the Water Exchange Rate
inferred← citeshttps://doi.org/10.1002/chem.200802318openalex-snapshot
Selective Iridium‐Catalyzed Alkylation of (Hetero)Aromatic Amines and Diamines with Alcohols under Mild Reaction Conditions
inferred← citeshttps://doi.org/10.1002/chem.200903178openalex-snapshot
Synthesis and Application of a New Fluorous‐Tagged Ammonia Equivalent
inferred← citeshttps://doi.org/10.1002/chem.201000011openalex-snapshot
Asymmetric Catalytic Hydrogenolysis of ArylHalide Bonds in Fused Arene Chromium and Ruthenium Complexes
inferred← citeshttps://doi.org/10.1002/chem.201002704openalex-snapshot
Microwave‐Promoted Selective Mono‐N‐Alkylation of Anilines with Tertiary Amines by Heterogeneous Catalysis
inferred← citeshttps://doi.org/10.1002/chem.201100393openalex-snapshot
Direct One‐Pot Reductive N‐Alkylation of Nitroarenes by using Alcohols with Supported Gold Catalysts
inferred← citeshttps://doi.org/10.1002/chem.201100818openalex-snapshot
Ultrathin Platinum Nanowire Catalysts for Direct CN Coupling of Carbonyls with Aromatic Nitro Compounds under 1 Bar of Hydrogen
inferred← citeshttps://doi.org/10.1002/chem.201103270openalex-snapshot
Synthesis of Aldehyde‐Linked Nucleotides and DNA and Their Bioconjugations with Lysine and Peptides through Reductive Amination
inferred← citeshttps://doi.org/10.1002/chem.201200376openalex-snapshot
Asymmetric Total Synthesis of (−)‐Stenine and 9a‐epi‐Stenine
inferred← citeshttps://doi.org/10.1002/chem.201200831openalex-snapshot
Rapid and Efficient Access to Secondary Arylmethylamines
inferred← citeshttps://doi.org/10.1002/chem.201203203openalex-snapshot
Toward the Total Synthesis of Haliclonin A: Construction of a Tricyclic Substructure
inferred← citeshttps://doi.org/10.1002/chem.201204194openalex-snapshot
Fast Reductive Amination by Transfer Hydrogenation “on Water”
inferred← citeshttps://doi.org/10.1002/chem.201302721openalex-snapshot
Determination of Amino Acid Enantiopurity and Absolute Configuration: Synergism between Configurationally Labile Metal‐Based Receptors and Dynamic Covalent Interactions
inferred← citeshttps://doi.org/10.1002/chem.201303541openalex-snapshot
Primary Amines by Transfer Hydrogenative Reductive Amination of Ketones by Using Cyclometalated IrIII Catalysts
inferred← citeshttps://doi.org/10.1002/chem.201403985openalex-snapshot
Palladium–N‐Heterocyclic Carbene (NHC)‐Catalyzed Asymmetric Synthesis of Indolines through Regiodivergent C(sp3)H Activation: Scope and DFT Study
inferred← citeshttps://doi.org/10.1002/chem.201501627openalex-snapshot
Novel Asymmetric Formylation of Aromatic Compounds: Enantioselective Synthesis of Formyl 7,8‐Dipropyltetrathia[7]helicenes
inferred← citeshttps://doi.org/10.1002/chem.201600989openalex-snapshot
Asymmetric Diels–Alder Cycloadditions of Trifluoromethylated Dienophiles Under Trienamine Catalysis
inferred← citeshttps://doi.org/10.1002/chem.201602454openalex-snapshot
Electrochemical Oxidative C−H/N−H Coupling between γ‐Lactams and Anilines
inferred← citeshttps://doi.org/10.1002/chem.201701254openalex-snapshot
Unsymmetrical Iron P‐NH‐P′ Catalysts for the Asymmetric Pressure Hydrogenation of Aryl Ketones
inferred← citeshttps://doi.org/10.1002/chem.201801046openalex-snapshot
Diastereoselective Synthesis of Highly Substituted, Amino‐ and Pyrrolidino‐Tetrahydrofurans as Lead‐Like Molecular Scaffolds
inferred← citeshttps://doi.org/10.1002/chem.201802468openalex-snapshot
Mixed‐Phase 2D‐MoS2 as an Effective Photocatalyst for Selective Aerobic Oxidative Coupling of Amines under Visible‐Light Irradiation
inferred← citeshttps://doi.org/10.1002/chem.202100238openalex-snapshot
Intermolecular Hydroaminoalkylation of Alkynes
inferred← citeshttps://doi.org/10.1002/chem.202201078openalex-snapshot
Iridium‐Catalyzed Direct Reductive Amination of Ketones and Secondary Amines: Breaking the Aliphatic Wall
inferred← citeshttps://doi.org/10.1002/chem.202303179openalex-snapshot
Aromatic C(sp2)−H Functionalization by Consecutive Paired Electrolysis: Dibromination of Aryl Amines with Dibromoethane at Room Temperature
inferred← citeshttps://doi.org/10.1002/chem.202401955openalex-snapshot
Chemical Predictive Modelling and Natural Product‐based Divergent Synthesis – Design of Type B PPAPs with Nanomolar Activities against MRSA
inferred← citeshttps://doi.org/10.1002/chem.202500059openalex-snapshot
Selective and Waste‐Free Isolation of High Purity Primary Amines from Amine and Reaction Mixtures by Selective Ammonium Carbamate Crystallization
inferred← citeshttps://doi.org/10.1002/chem.202502889openalex-snapshot
Pharmaceuticals Made with Hydrogen: A Sustainable and Efficient Approach Using Flow Synthesis
inferred← citeshttps://doi.org/10.1002/chin.199639094openalex-snapshot
ChemInform Abstract: Reductive Amination of Aldehydes and Ketones with Sodium Triacetoxyborohydride. Studies on Direct and Indirect Reductive Amination Procedures.
inferred← citeshttps://doi.org/10.1002/chin.200304276openalex-snapshot
Automated Purification Systems
inferred← citeshttps://doi.org/10.1002/chin.200532073openalex-snapshot
Catalytic Reductive Alkylation of Secondary Amine with Aldehyde and Silane by an Iridium Compound.
inferred← citeshttps://doi.org/10.1002/chin.200703235openalex-snapshot
A Review on the Use of Sodium Triacetoxyborohydride in the Reductive Amination of Ketones and Aldehydes
inferred← citeshttps://doi.org/10.1002/chir.20137openalex-snapshot
Stereoselective synthesis of an anti-HIV drug candidate
inferred← citeshttps://doi.org/10.1002/cjoc.200690074openalex-snapshot
Enantiospecific Synthesis of Penehyclidine Hydrochloride and Its Piperidine Derivatives with R Configuration
inferred← citeshttps://doi.org/10.1002/cjoc.200690153openalex-snapshot
One Pot Reduction of Imines Generated in‐situ from Aldehydes and Amines by the NaBH4‐InCl3 System
inferred← citeshttps://doi.org/10.1002/cjoc.201190155openalex-snapshot
A Fast and Highly Efficient Protocol for Reductive Amination of Aromatic Aldehydes Using NaBH4 and Isoxazole Amines in an Ionic Liquid Medium
inferred← citeshttps://doi.org/10.1002/cjoc.201200132openalex-snapshot
Reductive Amination of Aldehydes and Ketones with Primary Amines by Using Lithium Amidoborane as Reducing Reagent
inferred← citeshttps://doi.org/10.1002/cmdc.200500008openalex-snapshot
Unexpected Novel Binding Mode of Pyrrolidine‐Based Aspartyl Protease Inhibitors: Design, Synthesis and Crystal Structure in Complex with HIV Protease
inferred← citeshttps://doi.org/10.1002/cmdc.200700112openalex-snapshot
Design, Synthesis, and Pharmacological Evaluation of Mefloquine‐Based Ligands as Novel Antituberculosis Agents
inferred← citeshttps://doi.org/10.1002/cmdc.200800145openalex-snapshot
Discovery of Novel Non‐Cyclam Polynitrogenated CXCR4 Coreceptor Inhibitors
inferred← citeshttps://doi.org/10.1002/cmdc.200800314openalex-snapshot
From Molecular Shape to Potent Bioactive Agents II: Fragment‐Based de novo Design
inferred← citeshttps://doi.org/10.1002/cmdc.201000280openalex-snapshot
Towards the Discovery of New Hypnotic Agents: Synthesis and Preliminary Pharmacological Evaluation of a Novel Class of Dibenzo[a,d]cycloheptene Derivatives
inferred← citeshttps://doi.org/10.1002/cmdc.201100531openalex-snapshot
Design, Synthesis, and Biological Activity of Hydroxamic Tertiary Amines as Histone Deacetylase Inhibitors
inferred← citeshttps://doi.org/10.1002/cmdc.201300240openalex-snapshot
Aryl Biphenyl‐3‐ylmethylpiperazines as 5‐HT7 Receptor Antagonists
inferred← citeshttps://doi.org/10.1002/cmdc.201400034openalex-snapshot
Synthesis and DNA Cleavage Activity of Bis‐3‐chloropiperidines as Alkylating Agents
inferred← citeshttps://doi.org/10.1002/cmdc.201500510openalex-snapshot
Synthesis and Biopharmaceutical Evaluation of Imatinib Analogues Featuring Unusual Structural Motifs
inferred← citeshttps://doi.org/10.1002/cmdc.201600546openalex-snapshot
The Development of Next‐Generation Pyridinium‐Based multiQAC Antiseptics
inferred← citeshttps://doi.org/10.1002/cmdc.201700449openalex-snapshot
Design, Synthesis, Molecular Modeling, and Biological Evaluation of Novel Amine‐based Histone Deacetylase Inhibitors
inferred← citeshttps://doi.org/10.1002/cmdc.201900075openalex-snapshot
Optimization of Drug Candidates That Inhibit the D‐Loop Activity of RAD51
inferred← citeshttps://doi.org/10.1002/cmdc.201900719openalex-snapshot
N‐Substituted Nipecotic Acids as (S)‐SNAP‐5114 Analogues with Modified Lipophilic Domains
inferred← citeshttps://doi.org/10.1002/cmdc.202200026openalex-snapshot
Scaffold Hopping from Amodiaquine to Novel Nurr1 Agonist Chemotypes via Microscale Analogue Libraries
inferred← citeshttps://doi.org/10.1002/cmdc.202200113openalex-snapshot
Puckering the Planar Landscape of Fragments: Design and Synthesis of a 3D Cyclobutane Fragment Library
inferred← citeshttps://doi.org/10.1002/cmdc.202500298openalex-snapshot
Synthesis and Biological Characterization of 4,4‐Difluoro‐3‐(phenoxymethyl)piperidine Scaffold as Dopamine 4 Receptor (D 4 R) Antagonist in vitro Tool compounds
inferred← citeshttps://doi.org/10.1002/cphc.200290004openalex-snapshot
Cubic Mesophase in an Unsymmetrical Alkyl Ammonium Salt. Synthesis and Structural Model
inferred← citeshttps://doi.org/10.1002/cssc.201402413openalex-snapshot
Iron‐Catalyzed Synthesis of Secondary Amines: On the Way to Green Reductive Aminations
inferred← citeshttps://doi.org/10.1002/cssc.201802460openalex-snapshot
Band‐Gap Narrowing of Highly Stable Heterogeneous ZrO2–ZnO Nanocomposites for the Reductive Amination of Carbonyl Compounds with Formic Acid and Triethylamine
inferred← citeshttps://doi.org/10.1002/cssc.202300392openalex-snapshot
Directing the Selectivity of Oxygen Reduction to Water by Confining a Cu Catalyst in a Metal Organic Framework
inferred← citeshttps://doi.org/10.1002/ejic.200300667openalex-snapshot
Non‐Heme Iron Complexes for Stereoselective Oxidation: Tuning of the Selectivity in Dihydroxylation Using Different Solvents
inferred← citeshttps://doi.org/10.1002/ejic.200900875openalex-snapshot
Chiral [Bis(olefin)amine]rhodium(I) Complexes – Transfer Hydrogenation in Ethanol
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