On the public citation graph

Mercury-Catalyzed Rearrangement of Ketoximes into Amides and Lactams in Acetonitrile

https://doi.org/10.1021/jo070297k
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.
Claim with ORCID
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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

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(19991004)38:19<2910::aid-anie2910>3.0.co;2-copenalex-snapshot
Noncatalytic Organic Synthesis Using Supercritical Water: The Peculiarity Near the Critical Point
inferredcites →https://doi.org/10.1002/(sici)1521-3773(19991004)38:19<2914::aid-anie2914>3.0.co;2-popenalex-snapshot
A 1010 Rate Enhancement of Phosphodiester Hydrolysis by a Dinuclear Aminopeptidase—Transition-State Analogues as Substrates?
inferredcites →https://doi.org/10.1016/j.apcata.2005.03.045openalex-snapshot
Vapor-phase Beckmann rearrangement of cyclohexanone oxime over H3PO4/ZrO2–TiO2
inferredcites →https://doi.org/10.1016/j.tetlet.2004.04.068openalex-snapshot
Silica supported MoO 3 : a mild heterogeneous catalyst for the Beckmann rearrangement and its application to some sugar derived ketoximes
inferredcites →https://doi.org/10.1021/ja049363fopenalex-snapshot
Hydrogen Bond Driven Chemical Reactions: Beckmann Rearrangement of Cyclohexanone Oxime into ε-Caprolactam in Supercritical Water
inferredcites →https://doi.org/10.1021/ja053441xopenalex-snapshot
Cyanuric Chloride as a Mild and Active Beckmann Rearrangement Catalyst
inferredcites →https://doi.org/10.1081/scc-120004081openalex-snapshot
STUDIES IN BECKMANN REARRANGEMENT OF SUBSTITUTED BENZOPHENONE AND ACETOPHENONE OXIMES

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.4675520openalex-extracted
inferred← citeshttps://doi.org/10.1002/9780470975800.ch1openalex-snapshot
Reactions of Aldehydes and Ketones and their Derivatives
inferred← citeshttps://doi.org/10.1002/9780470975800.ch14openalex-snapshot
Molecular Rearrangements: Part 2. Other Reactions
inferred← citeshttps://doi.org/10.1002/9781118662083.cot09-007openalex-snapshot
Formation of Nitriles, Carboxylic Acids, and Derivatives by Rearrangements
inferred← citeshttps://doi.org/10.1002/9783527651733.ch27openalex-snapshot
Catalytic Amide Bond Forming Methods
inferred← citeshttps://doi.org/10.1002/9783527809080.cataz09420openalex-snapshot
ketoxime rearrangement
inferred← citeshttps://doi.org/10.1002/adsc.201200424openalex-snapshot
The Synthesis of N‐Arylated Amides via Copper(II) Triflate‐ Catalyzed Direct Oxygenation and N‐Arylation of Benzylamines with Aryl Iodides
inferred← citeshttps://doi.org/10.1002/adsc.201801096openalex-snapshot
Copper‐Catalyzed Site‐Selective Oxidative C−C Bond Cleavage of Simple Ketones for the Synthesis of Anilides and Paracetamol
inferred← citeshttps://doi.org/10.1002/adsc.201900279openalex-snapshot
Visible‐Light Mediated Photooxidative Synthesis of α‐Keto Amides
inferred← citeshttps://doi.org/10.1002/adsc.202001416openalex-snapshot
Ethyl 2‐Cyano‐2‐(2‐nitrobenzenesulfonyloxyimino) Acetate (ortho‐NosylOXY)‐Mediated Double Beckmann Rearrangement of Ketoximes under Microwave Irradiation: A Mechanistic Perception
inferred← citeshttps://doi.org/10.1002/ajoc.201700703openalex-snapshot
Copper‐Catalyzed Cyclization of Ketoxime Carboxylates and N‐Aryl Glycine Esters for the Synthesis of Pyridines
inferred← citeshttps://doi.org/10.1002/ange.201107079openalex-snapshot
Core‐Structure‐Oriented Asymmetric Organocatalytic Substitution of 3‐Hydroxyoxindoles: Application in the Enantioselective Total Synthesis of (+)‐Folicanthine
inferred← citeshttps://doi.org/10.1002/anie.201107079openalex-snapshot
Core‐Structure‐Oriented Asymmetric Organocatalytic Substitution of 3‐Hydroxyoxindoles: Application in the Enantioselective Total Synthesis of (+)‐Folicanthine
inferred← citeshttps://doi.org/10.1002/aoc.3744openalex-snapshot
Mild and eco‐friendly chemoselective acylation of amines in aqueous medium using a green, superparamagnetic, recoverable nanocatalyst
inferred← citeshttps://doi.org/10.1002/aoc.5855openalex-snapshot
Synthesis of acetamides via oxidative C–C bond cleavage of ketones catalyzed by Cu‐immobilized magnetic nanoparticles
inferred← citeshttps://doi.org/10.1002/asia.201100773openalex-snapshot
A Highly Efficient Friedel–Crafts Reaction of 3‐Hydroxyoxindoles and Aromatic Compounds to 3,3‐Diaryl and 3‐Alkyl‐3‐aryloxindoles Catalyzed by Hg(ClO4)2⋅3 H2O
inferred← citeshttps://doi.org/10.1002/cctc.202000156openalex-snapshot
N‐Heterocyclic Carbene/Cobalt Cooperative Catalysis for the Chemo‐ and Regioselective C−N Bond Formation between Aldehyde and Amines/Amides
inferred← citeshttps://doi.org/10.1002/cctc.202401563openalex-snapshot
Insight into Synergistic Brønsted and Lewis Acidic Deep Eutectic Solvent for Beckmann Rearrangement of Cyclohexanone Oxime
inferred← citeshttps://doi.org/10.1002/chem.201905358openalex-snapshot
Sulfuryl Fluoride Mediated Synthesis of Amides and Amidines from Ketoximes via Beckmann Rearrangement
inferred← citeshttps://doi.org/10.1002/chin.200742042openalex-snapshot
Mercury‐Catalyzed Rearrangement of Ketoximes into Amides and Lactams in Acetonitrile.
inferred← citeshttps://doi.org/10.1002/cjoc.200990224openalex-snapshot
Highly Efficient N‐Monomethylation of Primary Aryl Amines
inferred← citeshttps://doi.org/10.1002/cjoc.201190193openalex-snapshot
A Mild and Highly Efficient Catalyst for Beckmann Rearrangement, BF3·OEt2
inferred← citeshttps://doi.org/10.1002/cjoc.201700191openalex-snapshot
Carbon Tetrabromide/Triphenylphosphine‐Activated Beckmann Rearrangement of Ketoximes for Synthesis of Amides
inferred← citeshttps://doi.org/10.1002/cplu.202500577openalex-snapshot
Peculiarities of Mercuration–Iododemercuration of Propargyl Derivatives
inferred← citeshttps://doi.org/10.1002/ejoc.201200511openalex-snapshot
Phosphorus‐Containing Lewis Base Catalyzed Cascade Reactions of Isatin‐Derived Oximes with Allenic Esters and Further Transformations
inferred← citeshttps://doi.org/10.1002/ejoc.201301868openalex-snapshot
Copper‐Catalyzed Regioselective Synthesis of N ‐Aryl Amides from Aldoximes and Aryl Halides
inferred← citeshttps://doi.org/10.1002/ejoc.201900231openalex-snapshot
Visible Light‐Promoted Beckmann Rearrangements: Separating Sequential Photochemical and Thermal Phenomena in a Continuous Flow Reactor
inferred← citeshttps://doi.org/10.1002/hc.21273openalex-snapshot
Synthesis of New Phosphonoamide and Phosphonocaprolactam Derivatives via the Diethyl Chlorophosphate‐Promoted Beckmann Rearrangement of γ‐Phosphonyloximes
inferred← citeshttps://doi.org/10.1002/slct.201902432openalex-snapshot
Cadmium(II)‐Loaded Fe 3 O 4 @MPTS Nanoparticles: Preparation and Application as Catalyst for C‐N Coupling Reactions
inferred← citeshttps://doi.org/10.1002/slct.202000981openalex-snapshot
Oxidative Amidation of Aldehydes with Amines Catalysed by Fe(II) – Hydride Complex and N‐ Heterocyclic Carbenes (NHC)
inferred← citeshttps://doi.org/10.1002/slct.202203449openalex-snapshot
A Switchable Protocol for Selective Synthesis of gem ‐Dibromo Compounds and Amides from Ketoximes using TsNBr 2
inferred← citeshttps://doi.org/10.1002/slct.202302853openalex-snapshot
Comprehensive updates on Beckmann Rearrangement
inferred← citeshttps://doi.org/10.1002/slct.74730openalex-snapshot
Mercury(II) Salts‐Mediated Transformations of Acetylene Systems: Synthetic Perspectives
inferred← citeshttps://doi.org/10.1002/tcr.201800016openalex-snapshot
β‐Cyclodextrin: A Green and Efficient Supramolecular Catalyst for Organic Transformations
inferred← citeshttps://doi.org/10.1007/978-1-4020-9787-4_10openalex-snapshot
Addendum 2005–2008
inferred← citeshttps://doi.org/10.1007/s10562-015-1515-6openalex-snapshot
A Mechanochemical Approach for the Construction of Carbon–Carbon Double Bonds: Efficient Syntheses of Aryl/Heteroaryl/Aliphatic Acrylates and Nitriles
inferred← citeshttps://doi.org/10.1007/s10593-013-1309-yopenalex-snapshot
1,2-Di(4-R-furazan-3-yl)glyoximes: Synthesis by the Reduction of 3,4-Bis(4-R-furazan-3-yl)furoxans and Study of the Reactivity of these Compounds
inferred← citeshttps://doi.org/10.1007/s11164-011-0327-6openalex-snapshot
A facile and efficient method for the selective deacylation of N-arylacetamides and 2-chloro-N-arylacetamides catalyzed by SOCl2
inferred← citeshttps://doi.org/10.1007/s11172-010-0064-9openalex-snapshot
Synthesis of fluoromethyl-containing analogs of antitumor alkaloid luotonin A
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00622-4openalex-snapshot
6.14 Functional Group Transformations via Carbonyl Derivatives
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00730-8openalex-snapshot
7.25 The Beckmann and Related Reactions
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.80025-3openalex-snapshot
The Beckmann and Related Reactions
inferred← citeshttps://doi.org/10.1016/j.bmcl.2017.06.048openalex-snapshot
Synthesis and biological evaluation of novel steroidal 5α,8α-epidioxyandrost-6-ene-3β-ol-17-(O-phenylacetamide)oxime derivatives as potential anticancer agents
inferred← citeshttps://doi.org/10.1016/j.ces.2022.117519openalex-snapshot
High-yield and high-efficiency conversion of cyclohexanone oxime to ε-caprolactam in a green and facile reaction process over deep eutectic solvents
inferred← citeshttps://doi.org/10.1016/j.dyepig.2019.107854openalex-snapshot
A naphthalimide-based probe for phosgene sensing based on the phosgene-induced beckmann rearrangement
inferred← citeshttps://doi.org/10.1016/j.forc.2024.100558openalex-snapshot
Forensic implications of novel synthesis of cathinone derivatives by Neber and modified Neber rearrangements
inferred← citeshttps://doi.org/10.1016/j.fuel.2023.129777openalex-snapshot
Tailoring Zn-based diacidic functionalization of Deep eutectic solvent Catalyst: Green and efficient synthesis of ε-Caprolactam under mild conditions
inferred← citeshttps://doi.org/10.1016/j.fuel.2024.133977openalex-snapshot
One-pot realisation of reaction-extraction coupling: Innovative application and mechanistic insights of InCl3 deep eutectic solvents in Beckmann rearrangement reactions
inferred← citeshttps://doi.org/10.1016/j.ica.2009.05.017openalex-snapshot
Luminescent complexes of the zinc triad with N-substituted 8-amino-quinoline ligands: Synthesis and comparative study on the stability constants and related photophysical properties
inferred← citeshttps://doi.org/10.1016/j.ica.2019.119131openalex-snapshot
A new Schiff base fluorescent-colorimetric probe containing fluorene-naphthalene structure: Multifunction detection
inferred← citeshttps://doi.org/10.1016/j.ijoes.2025.101069openalex-snapshot
Electrocatalytic conversion of aromatic esters to ortho-aromatic ester amides using hydrophobic Cu-PTFE electrodes
inferred← citeshttps://doi.org/10.1016/j.jece.2017.02.009openalex-snapshot
Chemically treated eggshell wastes as a heterogeneous and eco-friendly catalyst for oximes preparation
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2014.10.017openalex-snapshot
NbCl5-mediated amidation of olefins with nitriles to secondary amides
inferred← citeshttps://doi.org/10.1016/j.micromeso.2024.113116openalex-snapshot
Improving the stability and reactivity of SAPO-11 catalyst for gas-phase beckmann rearrangement by a simple and effective alkali-treated approach
inferred← citeshttps://doi.org/10.1016/j.molstruc.2016.03.056openalex-snapshot
Synthesis, X-ray crystallography, spectroscopic (FT-IR, 1H &13C NMR and UV), computational (DFT/B3LYP) and enzymes inhibitory studies of 7-hydroximinocholest-5-en-3-ol acetate
inferred← citeshttps://doi.org/10.1016/j.molstruc.2016.05.085openalex-snapshot
Theoretical and experimental studies of 3β-acetoxy-5α-cholestan-6-one oxime
inferred← citeshttps://doi.org/10.1016/j.molstruc.2017.10.087openalex-snapshot
Synthesis, spectra and X-ray crystallography of dipyridin-2-ylmethanone oxime and its CuX 2 (oxime) 2 complexes: Thermal, Hirshfeld surface and DFT analysis
inferred← citeshttps://doi.org/10.1016/j.molstruc.2020.127848openalex-snapshot
Synthesis, crystal structure, DFT and biological activity of E-pyrene-1-carbaldehyde oxime and E-2-naphthaldehyde oxime
inferred← citeshttps://doi.org/10.1016/j.tet.2008.10.024openalex-snapshot
Microwave-assisted methylation of phenols with tetramethylammonium chloride in the presence of K2CO3 or Cs2CO3
inferred← citeshttps://doi.org/10.1016/j.tet.2009.07.036openalex-snapshot
Unexpected results from the re-investigation of the Beckmann rearrangement of ketoximes into amides by using TsCl
inferred← citeshttps://doi.org/10.1016/j.tet.2011.06.045openalex-snapshot
Practical synthesis of amides from alkynyl bromides, amines, and water
inferred← citeshttps://doi.org/10.1016/j.tet.2012.01.038openalex-snapshot
One-pot stibine modified Co2(CO)8 catalyzed reductive N-alkylation of primary amides with carbonyl compounds
inferred← citeshttps://doi.org/10.1016/j.tet.2015.03.071openalex-snapshot
N-Heterocyclic carbene-catalysed amidation of vinyl esters with aromatic amines
inferred← citeshttps://doi.org/10.1016/j.tet.2016.06.060openalex-snapshot
AIBN-promoted amidation of anilines with 1, 3-diketones via oxidative cleavage of C–C bond under aerobic conditions
inferred← citeshttps://doi.org/10.1016/j.tet.2019.04.056openalex-snapshot
o-Phthalic Anhydride/Zn(OTf)2 co-catalyzed Beckmann rearrangement under mild conditions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.05.113openalex-snapshot
Azido-Schmidt reaction for the formation of amides, imides and lactams from ketones in the presence of FeCl3
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.11.128openalex-snapshot
Bromodimethylsulfonium bromide (BDMS) in ionic liquid: a mild and efficient catalyst for Beckmann rearrangement
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.12.090openalex-snapshot
An efficient catalytic method for the Beckmann rearrangement of ketoximes to amides and aldoximes to nitriles mediated by propylphosphonic anhydride (T3P®)
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.07.032openalex-snapshot
Titanium cation-exchanged montmorillonite as an active heterogeneous catalyst for the Beckmann rearrangement under mild reaction conditions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.12.038openalex-snapshot
Keggin-type Bronsted dodecatungstophosphoric acid: a quasi homogenous and reusable catalyst system for liquid phase Beckmann rearrangement
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.02.110openalex-snapshot
A solvent-free one step conversion of ketones to amides via Beckmann rearrangement catalysed by FeCl3·6H2O in presence of hydroxylamine hydrochloride
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.12.060openalex-snapshot
CuCl/TBHP catalyzed synthesis of amides from aldehydes and amines in water
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.11.054openalex-snapshot
Lewis acid-assisted N-fluorobenzenesulfonimide-based electrophilic fluorine catalysis in Beckmann rearrangement
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.02.024openalex-snapshot
Amide bond synthesis via silver(I) N-heterocyclic carbene-catalyzed and tert-butyl hydroperoxide-mediated oxidative coupling of alcohols with amines under base free conditions
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00536openalex-snapshot
Coupling of Styrylmalonates with Furan and Benzofuran Carbaldehydes: Synthesis and Chemistry of Substituted (4-Oxocyclopent-2-enyl)malonates
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02478openalex-snapshot
Amidation of Enones via Beckmann Rearrangement
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02081openalex-snapshot
Synthesis of Polyfunctional Pyridines via Copper-Catalyzed Oxidative Coupling Reactions
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02731openalex-snapshot
Palladium-Catalyzed, ortho-Selective C–H Halogenation of Benzyl Nitriles, Aryl Weinreb Amides, and Anilides
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01810openalex-snapshot
Direct and Catalytic Amide Synthesis from Ketones via Transoximation and Beckmann Rearrangement under Mild Conditions
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02669openalex-snapshot
Microdroplets as Microreactors for Fast Synthesis of Ketoximes and Amides
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02168openalex-snapshot
Visible-Light-Induced Beckmann Rearrangement by Organic Photoredox Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01634openalex-snapshot
Radical Beckmann Rearrangement and Its Application in the Formal Total Synthesis of Antimalarial Natural Product Isocryptolepine via C–H Activation
inferred← citeshttps://doi.org/10.1021/acsomega.7b01028openalex-snapshot
Heterogeneous Route for the One-Pot Synthesis of N-Arylamides from Aldoximes and Aryl Halides Using the CuO/Carbon Material
inferred← citeshttps://doi.org/10.1021/acssuschemeng.1c07613openalex-snapshot
Reusable Deep Eutectic Solvents for Clean ε-Caprolactam Synthesis under Mild Conditions
inferred← citeshttps://doi.org/10.1021/cs400009wopenalex-snapshot
A Multifunction Pd/Sc(OTf)3/Ionic Liquid Catalyst System for the Tandem One-Pot Conversion of Phenol to ε-Caprolactam
inferred← citeshttps://doi.org/10.1021/ja9082649openalex-snapshot
Efficient Regio- and Stereoselective Formation of Azocan-2-ones via 8-Endo Cyclization of α-Carbamoyl Radicals
inferred← citeshttps://doi.org/10.1021/jo200284aopenalex-snapshot
Iron(II)-Catalyzed Amidation of Aldehydes with Iminoiodinanes at Room Temperature and under Microwave-Assisted Conditions
inferred← citeshttps://doi.org/10.1021/jo200925qopenalex-snapshot
Pd-Catalyzed Asymmetric Allylic Etherizations with Oximes by Chiral Alkene-Phosphine Ligands
inferred← citeshttps://doi.org/10.1021/jo3005827openalex-snapshot
Palladium-Catalyzed Amidation of Aryl Halides Using 2-Dialkylphosphino-2′-alkoxyl-1,1′-binaphthyl as Ligands
inferred← citeshttps://doi.org/10.1021/jo301466wopenalex-snapshot
Synthesis and Evaluation of a Photochromic Surfactant for Organic Reactions in Aqueous Media
inferred← citeshttps://doi.org/10.1021/jo301553vopenalex-snapshot
Aerobic Oxidative Amidation of Aromatic and Cinnamic Aldehydes with Secondary Amines by CuI/2-Pyridonate Catalytic System
inferred← citeshttps://doi.org/10.1021/jo301820vopenalex-snapshot
Synthesis, Structures, and Solid State Self-Assemblies of Formyl and Acetyl Substituted Triptycenes and Their Derivatives
inferred← citeshttps://doi.org/10.1021/jo301964mopenalex-snapshot
Palladium-Catalyzed Ortho-Alkoxylation of Anilides via C–H Activation
inferred← citeshttps://doi.org/10.1021/jo400278copenalex-snapshot
Mechanistic Insight into Self-Propagation of Organo-Mediated Beckmann Rearrangement: A Combined Experimental and Computational Study
inferred← citeshttps://doi.org/10.1021/jo400701vopenalex-snapshot
Thioacids Mediated Selective and Mild N-Acylation of Amines
inferred← citeshttps://doi.org/10.1021/ol202290yopenalex-snapshot
Copper-Catalyzed Coupling of Oxime Acetates with Aldehydes: A New Strategy for Synthesis of Pyridines
inferred← citeshttps://doi.org/10.1021/ol4023886openalex-snapshot
MnO2 Promoted Sequential C–O and C–N Bond Formation via C–H Activation of Methylarenes: A New Approach to Amides
inferred← citeshttps://doi.org/10.1021/ol702788jopenalex-snapshot
Mild Amidation of Aldehydes with Amines Mediated by Lanthanide Catalysts
inferred← citeshttps://doi.org/10.1038/s41467-018-07462-wopenalex-snapshot
Pd(OAc)2-catalyzed asymmetric hydrogenation of sterically hindered N-tosylimines
inferred← citeshttps://doi.org/10.1039/b910757fopenalex-snapshot
Geometry-dependent divergence in the gold-catalyzed redox cascade cyclization of o-alkynylaryl ketoximes and nitrones leading to isoindoles
inferred← citeshttps://doi.org/10.1039/b911844fopenalex-snapshot
Ketoximes to N-substituted thioamides via PSCl3 mediated Beckmann rearrangement
inferred← citeshttps://doi.org/10.1039/b921066kopenalex-snapshot
Direct selective oxygen-assisted acylation of amines driven by metallic silver surfaces: dimethylamine with formaldehyde
inferred← citeshttps://doi.org/10.1039/c0cc00815jopenalex-snapshot
Cyclopropenium ion catalysed Beckmann rearrangement
inferred← citeshttps://doi.org/10.1039/c0cs00196aopenalex-snapshot
Metal-catalysed approaches to amide bond formation
inferred← citeshttps://doi.org/10.1039/c3gc41548aopenalex-snapshot
AIBN-initiated metal free amidation of aldehydes using N-chloroamines
inferred← citeshttps://doi.org/10.1039/c3gc41800fopenalex-snapshot
Copper-catalyzed homocoupling of ketoxime carboxylates for synthesis of symmetrical pyrroles
inferred← citeshttps://doi.org/10.1039/c3nj00870copenalex-snapshot
Visible-light-mediated eosin Y catalyzed aerobic desulfurization of thioamides into amides
inferred← citeshttps://doi.org/10.1039/c3ob41218kopenalex-snapshot
DDQ-promoted direct transformation of benzyl hydrocarbons to amides via tandem reaction of the CDC reaction and Beckmann rearrangement
inferred← citeshttps://doi.org/10.1039/c4cc10273hopenalex-snapshot
AIEE active perylene bisimide supported mercury nanoparticles for synthesis of amides via aldoximes/ketoximes rearrangement
inferred← citeshttps://doi.org/10.1039/c4gc00558aopenalex-snapshot
Magnetically recyclable magnetite–palladium (Nanocat-Fe–Pd) nanocatalyst for the Buchwald–Hartwig reaction
inferred← citeshttps://doi.org/10.1039/c4ra14234aopenalex-snapshot
Base-catalyzed synthesis of amides and imines via C–C and CC bond cleavage
inferred← citeshttps://doi.org/10.1039/c4ra15140bopenalex-snapshot
Copper catalysed C–N bond formation via a sequential acylation and deacylation process: a novel strategy for the synthesis of benzanilides
inferred← citeshttps://doi.org/10.1039/c5ra07789copenalex-snapshot
Highly efficient synthesis of amides from ketoximes using trifluoromethanesulphonic anhydride
inferred← citeshttps://doi.org/10.1039/c6qo00809gopenalex-snapshot
Synthesis of tetrasubstituted symmetrical pyridines by iron-catalyzed cyclization of ketoxime acetates
inferred← citeshttps://doi.org/10.1039/c7cc09491dopenalex-snapshot
Mild, calcium catalysed Beckmann rearrangements
inferred← citeshttps://doi.org/10.1039/c7ob01235gopenalex-snapshot
Metal-free synthesis of isatin oximes via radical coupling reactions of oxindoles with t-BuONO in water
inferred← citeshttps://doi.org/10.1039/c8nj05288copenalex-snapshot
Vilsmeier–Haack reagent mediated synthetic transformations with an immobilized iridium complex photoredox catalyst
inferred← citeshttps://doi.org/10.1039/c9ob00699kopenalex-snapshot
Clickable coupling of carboxylic acids and amines at room temperature mediated by SO 2 F 2 : a significant breakthrough for the construction of amides and peptide linkages
inferred← citeshttps://doi.org/10.1039/d0nj02034fopenalex-snapshot
Beckmann rearrangement catalysis: a review of recent advances
inferred← citeshttps://doi.org/10.1039/d0qo01401jopenalex-snapshot
Brønsted acid-catalyzed homogeneous O–H and S–H insertion reactions under metal- and ligand-free conditions
inferred← citeshttps://doi.org/10.1039/d1nj01987bopenalex-snapshot
Copper-catalyzed efficient access to 2,4,6-triphenyl pyridines via oxidative decarboxylative coupling of aryl acetic acids with oxime acetates
inferred← citeshttps://doi.org/10.1039/d2nj02755kopenalex-snapshot
Metal-free synthesis of secondary amides using N -Boc- O -tosylhydroxylamine as nitrogen source via Beckmann rearrangement
inferred← citeshttps://doi.org/10.1039/d2ra00897aopenalex-snapshot
N-Heterocyclic carbene (NHC)-catalyzed oxidation of unactivated aldimines to amides via imine umpolung under aerobic conditions
inferred← citeshttps://doi.org/10.1039/d5ra02843dopenalex-snapshot
Beckmann rearrangement of ketoximes for accessing amides and lactams promoted by a perimidine-2-thione supported Hg( ii ) complex: a mechanistic perception
inferred← citeshttps://doi.org/10.1039/d6nj00636aopenalex-snapshot
Nanostructured BiSI-catalyzed one-pot photoredox amidation, thioesterification and thiol–ene/yne click reactions via radical mechanism under visible light
inferred← citeshttps://doi.org/10.1039/d6ob01245kopenalex-snapshot
N -Acetylation of aromatic amines using copper acetate as an acetyl source
inferred← citeshttps://doi.org/10.1055/s-0039-1690005openalex-snapshot
Cu(OTf)2-Catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA)
inferred← citeshttps://doi.org/10.1055/sos-sd-127-00117openalex-snapshot
27.15 Product Class 15: Oximes
inferred← citeshttps://doi.org/10.1080/00397911.2011.585270openalex-snapshot
Ph3P/I2-Catalyzed Beckmann Rearrangement of Ketoximes into Amides
inferred← citeshttps://doi.org/10.1080/00397911003629416openalex-snapshot
Facile AlCl 3 -Promoted Catalytic Beckmann Rearrangement of Ketoximes
inferred← citeshttps://doi.org/10.1080/01614940.2019.1650876openalex-snapshot
An overview of caprolactam synthesis
inferred← citeshttps://doi.org/10.1186/2191-2858-1-12openalex-snapshot
A rapid, convenient, solventless green approach for the synthesis of oximes using grindstone chemistry
inferred← citeshttps://doi.org/10.17807/orbital.v15i4.18631openalex-snapshot
Unexpected Dimerizations of Arylfurfural Oximes in their Mass Spectra
inferred← citeshttps://doi.org/10.2174/0122133461349649241029175504openalex-snapshot
Recent Advances on Oximes Derivatives: Green Catalysis and Various Synthetic Routes
inferred← citeshttps://doi.org/10.2174/1385272827666230817144738openalex-snapshot
TiO2/SO42- Solid Superacid: A Rapid, Solventless, Recoverable Nanocatalyst for Eco-Friendly Synthesis of Piperidin-4-one Oximes
inferred← citeshttps://doi.org/10.3184/030823408x340780openalex-snapshot
Microwave Reaction of Diazonium Salts with Nitriles
inferred← citeshttps://doi.org/10.3329/bjsir.v48i1.15383openalex-snapshot
Studies on the conversion of ketones of heterocyclic spiro compounds having barbituric acid moieties into oxime derivatives
inferred← citeshttps://doi.org/10.3390/molecules171113662openalex-snapshot
Beckmann Rearrangement of Ketoximes Induced by Phenyl Dichlorophosphate at Ambient Temperature
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/10.3390/molecules27175450openalex-snapshot
N-Formylsaccharin: A Sweet(able) Formylating Agent in Mechanochemistry
inferred← citeshttps://doi.org/10.3390/molecules28124766openalex-snapshot
Synthesis, Crystal Structure, DFT, and Anticancer Activity of Some Imine-Type Compounds via Routine Schiff Base Reaction: An Example of Unexpected Cyclization to Oxazine Derivative
inferred← citeshttps://doi.org/10.3762/bjoc.17.153openalex-snapshot
Advances in mercury(II)-salt-mediated cyclization reactions of unsaturated bonds
inferred← citeshttps://doi.org/10.3762/bjoc.20.168openalex-snapshot
Negishi-coupling-enabled synthesis of α-heteroaryl-α-amino acid building blocks for DNA-encoded chemical library applications
inferred← citeshttps://doi.org/10.4028/www.scientific.net/amm.431.14openalex-snapshot
Industrial Fresh Fluorgypsum Catalyzed Beckmann Rearrangement of Ketoximes
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.