On the public citation graph
Transition metal catalysis and nucleophilic fluorination
0 signed · 479 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known work and none has been retracted — and get a dated CiteStamped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)1521-3773(19980420)37:7<994::aid-anie994>3.0.co;2-hopenalex-snapshot
Generation of “Naked” Fluoride Ions in Unprecedentedly High Concentrations from a Fluoropalladium Complex
inferredcites →https://doi.org/10.1002/(sici)1522-2675(19991215)82:12<2448::aid-hlca2448>3.0.co;2-gopenalex-snapshot
Carbon−Fluorine Bond Formationvia a Five-Coordinate Fluoro Complex of Ruthenium(II), Preliminary Communication
inferredcites →https://doi.org/10.1002/1521-3765(20020301)8:5<1006::aid-chem1006>3.0.co;2-mopenalex-snapshot
Palladium Fluoride Complexes: One More Step toward Metal-Mediated C−F Bond Formation Frontispiece shows woodcuts from: John French, The Art of Distillation, London, 1651. Courtesy of Adam McLean (http://www.levity.com/alchemy/).
inferredcites →https://doi.org/10.1002/1615-4169(200202)344:2<165::aid-adsc165>3.0.co;2-1openalex-snapshot
(Salen)chromium Complex Mediated Asymmetric Ring Opening of meso- and Racemic Epoxides with Different Fluoride Sources
inferredcites →https://doi.org/10.1002/adsc.201000624openalex-snapshot
Recent Advances in Catalytic Enantioselective Fluorination Reactions
inferredcites →https://doi.org/10.1002/ange.200500571openalex-snapshot
Direct Asymmetric α‐Fluorination of Aldehydes
inferredcites →https://doi.org/10.1002/ange.200803150openalex-snapshot
Tetrabutylammonium Tetra(tert‐Butyl Alcohol)‐Coordinated Fluoride as a Facile Fluoride Source
inferredcites →https://doi.org/10.1002/anie.200351405openalex-snapshot
Regio‐ and Enantioselective Synthesis of Allylic Fluorides by Electrophilic Fluorodesilylation of Allyl Silanes
inferredcites →https://doi.org/10.1002/anie.200500395openalex-snapshot
Enantioselective Formation of Stereogenic Carbon–Fluorine Centers by a Simple Catalytic Method
inferredcites →https://doi.org/10.1002/anie.200500571openalex-snapshot
Direct Asymmetric α‐Fluorination of Aldehydes
inferredcites →https://doi.org/10.1002/anie.200800717openalex-snapshot
Cinchona Alkaloid Catalyzed Enantioselective Fluorination of Allyl Silanes, Silyl Enol Ethers, and Oxindoles
inferredcites →https://doi.org/10.1002/anie.200802164openalex-snapshot
Palladium‐Mediated Fluorination of Arylboronic Acids
inferredcites →https://doi.org/10.1002/anie.200803150openalex-snapshot
Tetrabutylammonium Tetra(tert‐Butyl Alcohol)‐Coordinated Fluoride as a Facile Fluoride Source
inferredcites →https://doi.org/10.1002/anie.200804310openalex-snapshot
Palladium‐Catalyzed Substitution of Allylic Fluorides
inferredcites →https://doi.org/10.1002/anie.200902121openalex-snapshot
Transition‐Metal‐Mediated Reactions for CF Bond Construction: The State of Play
inferredcites →https://doi.org/10.1002/anie.201007307openalex-snapshot
Palladium‐Catalyzed Allylic Fluorination
inferredcites →https://doi.org/10.1002/anie.201103151openalex-snapshot
Organocatalyzed Enantioselective Fluorocyclizations
inferredcites →https://doi.org/10.1002/anie.201104652openalex-snapshot
Accelerating Palladium‐Catalyzed CF Bond Formation: Use of a Microflow Packed‐Bed Reactor
inferredcites →https://doi.org/10.1002/cbic.200300833openalex-snapshot
The Unique Role of Fluorine in the Design of Active Ingredients for Modern Crop Protection
inferredcites →https://doi.org/10.1002/ejic.200500795openalex-snapshot
Interactions of Cationic Palladium( II )‐ and Platinum( II )‐η3‐Allyl Complexes with Fluoride: Is Asymmetric Allylic Fluorination a Viable Reaction?
inferredcites →https://doi.org/10.1002/ejoc.200500708openalex-snapshot
Effect of the Leaving Group on the Rate and Mechanism of the Palladium‐Catalyzed Isomerization of Cyclic Allylic Benzoates in Allylic Substitutions
inferredcites →https://doi.org/10.1002/ijch.199100003openalex-snapshot
On the Mechanism of Palladium(0)‐Catalyzed Reactions of Allylic Substrates with Nucleophiles. Origin of the Loss of Stereospecificity
inferredcites →https://doi.org/10.1002/tcr.20017openalex-snapshot
Development of catalytic asymmetric reactions via chiral palladium enolates
inferredcites →https://doi.org/10.1016/j.jfluchem.2009.02.012openalex-snapshot
On the isolation of neat allylic fluorides
inferredcites →https://doi.org/10.1016/j.jfluchem.2009.05.008openalex-snapshot
Asymmetric oxidative α-fluorination of 2-alkylphenylacetaldehydes with AgHF2 and ruthenium/PNNP catalysts
inferredcites →https://doi.org/10.1016/j.jfluchem.2011.02.017openalex-snapshot
Aryne-mediated fluorination: Synthesis of fluorinated biaryls via a sequential desilylation–halide elimination–fluoride addition process
inferredcites →https://doi.org/10.1016/s0022-1139(00)00249-9openalex-snapshot
Enantioselective introduction of fluoride into organic compounds
inferredcites →https://doi.org/10.1016/s0022-1139(01)00486-9openalex-snapshot
Enantioselective ring-opening of epoxides by HF-reagents
inferredcites →https://doi.org/10.1016/s0040-4020(01)80768-7openalex-snapshot
Electronic control of enantioselectivity in the palladium-catalyzed asymmetric allylic substitution of trans 4-tbutyl-l-vinylcyclohexyl benzoates
inferredcites →https://doi.org/10.1016/s0040-4039(00)82271-6openalex-snapshot
New fluorinating reagents - I. The first enantioselective fluorination reaction
inferredcites →https://doi.org/10.1016/s0957-4166(96)00486-7openalex-snapshot
A remarkable anion effect on the enantioselectivity of the Pd-catalyzed allylic amination using ferrocenyl ligands
inferredcites →https://doi.org/10.1021/ar9001763openalex-snapshot
The Organometallic Fluorine Chemistry of Palladium and Rhodium: Studies toward Aromatic Fluorination
inferredcites →https://doi.org/10.1021/cr020027wopenalex-snapshot
Asymmetric Transition-Metal-Catalyzed Allylic Alkylations: Applications in Total Synthesis
inferredcites →https://doi.org/10.1021/cr068410eopenalex-snapshot
The Chemistry of Propargylic and Allylic Fluorides
inferredcites →https://doi.org/10.1021/cr800221vopenalex-snapshot
Update 1 of: Asymmetric Fluorination, Trifluoromethylation, and Perfluoroalkylation Reactions
inferredcites →https://doi.org/10.1021/cr9409804openalex-snapshot
Asymmetric Transition Metal-Catalyzed Allylic Alkylations
inferredcites →https://doi.org/10.1021/ja00043a034openalex-snapshot
Isomerization of (.pi.-allyl)palladium complexes via nucleophilic displacement by palladium(0). A common mechanism in palladium(0)-catalyzed allylic substitution
inferredcites →https://doi.org/10.1021/ja00050a013openalex-snapshot
A modular approach for ligand design for asymmetric allylic alkylations via enantioselective palladium-catalyzed ionizations
inferredcites →https://doi.org/10.1021/ja00155a012openalex-snapshot
Synthesis and Chemistry of the Aryliridium(III) Fluorides Cp'Ir(PMe3)(Aryl)F: High Reactivity due to Surprisingly Easy Ir-F Ionization
inferredcites →https://doi.org/10.1021/ja00163a060openalex-snapshot
Novel dependency of stereochemistry upon metal, ligand, and solvent in oxidative addition of allylic chloride to palladium(0) and platinum(0) complexes
inferredcites →https://doi.org/10.1021/ja0034592openalex-snapshot
Reductive Elimination of Aryl Halides from Palladium(II)
inferredcites →https://doi.org/10.1021/ja0440497openalex-snapshot
Anhydrous Tetrabutylammonium Fluoride
inferredcites →https://doi.org/10.1021/ja051805fopenalex-snapshot
Enantioselective Organocatalytic α-Fluorination of Aldehydes
inferredcites →https://doi.org/10.1021/ja054506zopenalex-snapshot
The F/Ph Rearrangement Reaction of [(Ph3P)3RhF], the Fluoride Congener of Wilkinson's Catalyst
inferredcites →https://doi.org/10.1021/ja061943kopenalex-snapshot
Palladium-Catalyzed Fluorination of Carbon−Hydrogen Bonds
inferredcites →https://doi.org/10.1021/ja066930lopenalex-snapshot
Aryl-Fluoride Reductive Elimination from Pd(II): Feasibility Assessment from Theory and Experiment
inferredcites →https://doi.org/10.1021/ja0723784openalex-snapshot
Reversible C−F Bond Formation and the Au-Catalyzed Hydrofluorination of Alkynes
inferredcites →https://doi.org/10.1021/ja100161dopenalex-snapshot
Enantioselective Ring Opening of Epoxides by Fluoride Anion Promoted by a Cooperative Dual-Catalyst System
inferredcites →https://doi.org/10.1021/ja106343hopenalex-snapshot
Discovery of 4- tert -Butyl-2,6-dimethylphenylsulfur Trifluoride as a Deoxofluorinating Agent with High Thermal Stability as Well as Unusual Resistance to Aqueous Hydrolysis, and Its Diverse Fluorination Capabilities Including Deoxofluoro-Arylsulfinylation with High Stereoselectivity
inferredcites →https://doi.org/10.1021/ja109120nopenalex-snapshot
Palladium-Catalyzed Asymmetric Synthesis of Allylic Fluorides
inferredcites →https://doi.org/10.1021/ja2058567openalex-snapshot
Nucleophilic Aryl Fluorination and Aryl Halide Exchange Mediated by a CuI/CuIII Catalytic Cycle
inferredcites →https://doi.org/10.1021/ja206960kopenalex-snapshot
Palladium-Catalyzed Regio- and Enantioselective Fluorination of Acyclic Allylic Halides
inferredcites →https://doi.org/10.1021/ja207256sopenalex-snapshot
Mechanistic Investigations of Cooperative Catalysis in the Enantioselective Fluorination of Epoxides
inferredcites →https://doi.org/10.1021/ja208461kopenalex-snapshot
Evidence for in Situ Catalyst Modification during the Pd-Catalyzed Conversion of Aryl Triflates to Aryl Fluorides
inferredcites →https://doi.org/10.1021/ja2087213openalex-snapshot
Iridium-Catalyzed Allylic Fluorination of Trichloroacetimidates
inferredcites →https://doi.org/10.1021/ja8055358openalex-snapshot
A Highly Active Catalyst for Pd-Catalyzed Amination Reactions: Cross-Coupling Reactions Using Aryl Mesylates and the Highly Selective Monoarylation of Primary Amines Using Aryl Chlorides
inferredcites →https://doi.org/10.1021/ja8099757openalex-snapshot
Structure-Based Rationale for Selectivity in the Asymmetric Allylic Alkylation of Cycloalkenyl Esters Employing the Trost ‘Standard Ligand’ (TSL): Isolation, Analysis and Alkylation of the Monomeric form of the Cationic η 3 -Cyclohexenyl Complex [(η 3 - c -C 6 H 9 )Pd(TSL)] +
inferredcites →https://doi.org/10.1021/ja909371topenalex-snapshot
Mechanism of C−F Reductive Elimination from Palladium(IV) Fluorides
inferredcites →https://doi.org/10.1021/ja963984uopenalex-snapshot
Molecular Fluoro Palladium Complexes
inferredcites →https://doi.org/10.1021/jm800219fopenalex-snapshot
The Many Roles for Fluorine in Medicinal Chemistry
inferredcites →https://doi.org/10.1021/jo00893a007openalex-snapshot
New fluorinating reagents. Dialkylaminosulfur fluorides
inferredcites →https://doi.org/10.1021/jo01336a027openalex-snapshot
Synthetic methods and reactions. 63. Pyridinium poly(hydrogen fluoride) (30% pyridine-70% hydrogen fluoride): a convenient reagent for organic fluorination reactions
inferredcites →https://doi.org/10.1021/jo9601270openalex-snapshot
The First Enantiocontrolled Synthesis of E,E Conjugated Dienes with a Fluorine Atom in the Allylic Position
inferredcites →https://doi.org/10.1021/ol0518535openalex-snapshot
Synthesis of Novel Enantiopure Fluorinated Building Blocks from Acyclic Chiral Allylsilanes
inferredcites →https://doi.org/10.1021/ol9016782openalex-snapshot
Regio- and Stereoselective Synthesis of Fluoroalkenes by Directed Au(I) Catalysis
inferredcites →https://doi.org/10.1021/om0000156openalex-snapshot
Toward Metal-Mediated C−F Bond Formation. Synthesis and Reactivity of the 16-Electron Fluoro Complex [RuF(dppp)2]PF6 (dppp = 1,3-Bis(diphenylphosphino)propane)
inferredcites →https://doi.org/10.1021/om010288gopenalex-snapshot
Catalytic Fluorination by Halide Exchange with 16-Electron Ruthenium(II) Complexes. X-ray Structure of [Tl(μ-F)2Ru(dppe)2]PF6
inferredcites →https://doi.org/10.1021/om050619fopenalex-snapshot
A Carbene-Stabilized Gold(I) Fluoride: Synthesis and Theory
inferredcites →https://doi.org/10.1021/om700469kopenalex-snapshot
Ar−F Reductive Elimination from Palladium(II) Revisited
inferredcites →https://doi.org/10.1038/nchem.351openalex-snapshot
Total synthesis and study of 6-deoxyerythronolide B by late-stage C–H oxidation
inferredcites →https://doi.org/10.1039/a808517jopenalex-snapshot
Bis(2-methoxyethyl)aminosulfur trifluoride: a new broad-spectrum deoxofluorinating agent with enhanced thermal stability
inferredcites →https://doi.org/10.1039/b317004gopenalex-snapshot
Enantioselective halogenation reactions
inferredcites →https://doi.org/10.1039/b513399hopenalex-snapshot
Electrophilic fluorination of organosilanes
inferredcites →https://doi.org/10.1039/b711844aopenalex-snapshot
Understanding organofluorine chemistry. An introduction to the C–F bond
inferredcites →https://doi.org/10.1039/b909566gopenalex-snapshot
Fluorine & chirality: how to create a nonracemic stereogenic carbon–fluorine centre?
inferredcites →https://doi.org/10.1126/science.1178239openalex-snapshot
Formation of ArF from LPdAr(F): Catalytic Conversion of Aryl Triflates to Aryl Fluorides
inferredcites →https://doi.org/10.1126/science.1212625openalex-snapshot
A Fluoride-Derived Electrophilic Late-Stage Fluorination Reagent for PET Imaging
inferredcites →https://doi.org/10.1246/bcsj.52.3377openalex-snapshot
F -Propene-Dialkylamine Reaction Products as Fluorinating Agents
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.4090903openalex-extracted
Checking the Stability of 18F of 2-Methylbenzenesulfonyl Fluoride and 2,4,6-Trimethylbenzenesulfonyl Fluoride in Rat Serum and PBS, Influence of Reaction Based on Electrons Pushing in the Aromatic (Donating and Withdrawing) and the Positions of Methyl Group
inferred← citeshttps://doi.org/10.1002/0471264180.or104.03openalex-snapshot
Transition‐Metal‐Mediated and Transition‐Metal‐Catalyzed Carbon–Fluorine Bond Formation
inferred← citeshttps://doi.org/10.1002/9781118341155.ch7openalex-snapshot
Practical Applications of Polyvalent Iodine Compounds
inferred← citeshttps://doi.org/10.1002/adsc.201400101openalex-snapshot
Palladium‐Catalyzed CF Bond Formation via Directed CH Activation
inferred← citeshttps://doi.org/10.1002/adsc.201400649openalex-snapshot
Asymmetric Michael Addition of 5 H‐Oxazol‐4‐ones to Vinyl Sulfones: Stereoselective Synthesis of Monofluorinated Analogs of 2‐Tertiary Hydroxyl‐3‐Methyl‐Substituted Carboxylic Acidl Derivatives
inferred← citeshttps://doi.org/10.1002/adsc.201500321openalex-snapshot
Palladium‐Catalysed CH Bond Electrophilic Fluorination of Highly Substituted Arylpyrazoles: Experimental and DFT Mechanistic Insights
inferred← citeshttps://doi.org/10.1002/adsc.201500744openalex-snapshot
A Combination of Metal and Organic Catalysis: Highly Diastereo‐ and Enantioselective Construction of Fluorinated 2‐Aminocyclopenta[b]pyran Derivatives
inferred← citeshttps://doi.org/10.1002/adsc.201501021openalex-snapshot
Zinc‐Catalyzed Stereo‐ and Regioselective 1,4‐Hydrative Fluorination of 3‐En‐1‐ynamides with Selectfluor
inferred← citeshttps://doi.org/10.1002/adsc.201501028openalex-snapshot
Direct Decarboxylative Alkynylation of α,α‐Difluoroarylacetic Acids under Transition Metal‐Free Conditions
inferred← citeshttps://doi.org/10.1002/adsc.201600835openalex-snapshot
Asymmetric Biocatalytic Synthesis of Fluorinated Pyridines through Transesterification or Transamination: Computational Insights into the Reactivity of Transaminases
inferred← citeshttps://doi.org/10.1002/adsc.201701229openalex-snapshot
Distal Functional Group Migration for Visible‐light Induced Carbo‐difluoroalkylation/monofluoroalkylation of Unactivated Alkenes
inferred← citeshttps://doi.org/10.1002/adsc.202301256openalex-snapshot
Silver‐Catalyzed Decarboxylative Acylfluorination of Two Alkenes with Ketonic Acids
inferred← citeshttps://doi.org/10.1002/advs.202305006openalex-snapshot
A Catalytic Three‐Component Aminofluorination of Unactivated Alkenes with Electron‐Rich Amino Sources
inferred← citeshttps://doi.org/10.1002/ajoc.201600383openalex-snapshot
Catalytic Cycloisomerization–Fluorination Sequence of N‐Propargyl Amides by Iodoarene/HF⋅Pyridine/Selectfluor Systems
inferred← citeshttps://doi.org/10.1002/ajoc.202200325openalex-snapshot
Recent Developments in Nucleophilic Fluorination with Potassium Fluoride (KF): A Review
inferred← citeshttps://doi.org/10.1002/ange.201205260openalex-snapshot
Synthese fluorierter Bausteine durch Übergangsmetall‐vermittelte Hydrodefluorierungsreaktionen
inferred← citeshttps://doi.org/10.1002/ange.201207356openalex-snapshot
Rhodium‐Catalyzed Enantioselective Nucleophilic Fluorination: Ring Opening of Oxabicyclic Alkenes
inferred← citeshttps://doi.org/10.1002/ange.201301097openalex-snapshot
Manganese‐Catalyzed Oxidative Benzylic C–H Fluorination by Fluoride Ions
inferred← citeshttps://doi.org/10.1002/ange.201301891openalex-snapshot
Copper‐Catalyzed Regioselective Fluorination of Allylic Halides
inferred← citeshttps://doi.org/10.1002/ange.201305106openalex-snapshot
Insertion of CS2 into Iridium–Fluorine Bonds
inferred← citeshttps://doi.org/10.1002/ange.201308071openalex-snapshot
Kinetic Resolution of Allyl Fluorides by Enantioselective Allylic Trifluoromethylation Based on Silicon‐Assisted CF Bond Cleavage
inferred← citeshttps://doi.org/10.1002/ange.201309535openalex-snapshot
Palladium‐Catalyzed Difluoroalkylation of Aryl Boronic Acids: A New Method for the Synthesis of Aryldifluoromethylated Phosphonates and Carboxylic Acid Derivatives
inferred← citeshttps://doi.org/10.1002/ange.201402238openalex-snapshot
Mild Copper‐Catalyzed Fluorination of Alkyl Triflates with Potassium Fluoride
inferred← citeshttps://doi.org/10.1002/ange.201404423openalex-snapshot
Mild and Versatile Nitrate‐Promoted CH Bond Fluorination
inferred← citeshttps://doi.org/10.1002/ange.201405653openalex-snapshot
Nickel‐Catalyzed Cross‐Coupling of Functionalized Difluoromethyl Bromides and Chlorides with Aryl Boronic Acids: A General Method for Difluoroalkylated Arenes
inferred← citeshttps://doi.org/10.1002/ange.201410288openalex-snapshot
Fluorierung in späten Synthesestadien: extravagante Neuheit oder nützliches Hilfsmittel?
inferred← citeshttps://doi.org/10.1002/ange.201410954openalex-snapshot
Condensed‐Phase, Halogen‐Bonded CF3I and C2F5I Adducts for Perfluoroalkylation Reactions
inferred← citeshttps://doi.org/10.1002/ange.201500399openalex-snapshot
Targeted Fluorination with the Fluoride Ion by Manganese‐Catalyzed Decarboxylation
inferred← citeshttps://doi.org/10.1002/ange.201502882openalex-snapshot
Facile Access to Fluoromethylated Arenes by Nickel‐Catalyzed Cross‐Coupling between Arylboronic Acids and Fluoromethyl Bromide
inferred← citeshttps://doi.org/10.1002/ange.201506882openalex-snapshot
Catalytic Nucleophilic Fluorination of Secondary and Tertiary Propargylic Electrophiles with a Copper–N‐Heterocyclic Carbene Complex
inferred← citeshttps://doi.org/10.1002/ange.201511321openalex-snapshot
Nickel‐Catalyzed Decarboxylative Difluoroalkylation of α,β‐Unsaturated Carboxylic Acids
inferred← citeshttps://doi.org/10.1002/ange.201603210openalex-snapshot
Asymmetrische Desymmetrisierung durch metallfreie C‐F‐Bindungsaktivierung: Synthese von 3,5‐Diaryl‐5‐fluormethyl‐oxazolidin‐2‐onen mit quartären Kohlenstoffzentren
inferred← citeshttps://doi.org/10.1002/ange.201603426openalex-snapshot
Site‐Selective Tertiary Alkyl–Fluorine Bond Formation from α‐Bromoamides Using a Copper/CsF Catalyst System
inferred← citeshttps://doi.org/10.1002/ange.201610047openalex-snapshot
Nickel(0)‐Mediated Transformation of Tetrafluoroethylene and Vinylarenes into Fluorinated Cyclobutyl Compounds
inferred← citeshttps://doi.org/10.1002/ange.201708003openalex-snapshot
Transition‐Metal‐Free Catalytic Hydrodefluorination of Polyfluoroarenes by Concerted Nucleophilic Aromatic Substitution with a Hydrosilicate
inferred← citeshttps://doi.org/10.1002/ange.201708197openalex-snapshot
Selective Radical Fluorination of Tertiary Alkyl Halides at Room Temperature
inferred← citeshttps://doi.org/10.1002/ange.201801280openalex-snapshot
Benzylic Fluorination of Aza‐Heterocycles Induced by Single‐Electron Transfer to Selectfluor
inferred← citeshttps://doi.org/10.1002/ange.201808021openalex-snapshot
Selective C(sp3)−H and C(sp2)−H Fluorination of Alcohols Using Practical Auxiliaries
inferred← citeshttps://doi.org/10.1002/ange.201812927openalex-snapshot
Regioselective Vinylation of Remote Unactivated C(sp3)−H Bonds: Access to Complex Fluoroalkylated Alkenes
inferred← citeshttps://doi.org/10.1002/ange.201813591openalex-snapshot
Palladium(II)‐Catalyzed Enantioselective Aminotrifluoromethoxylation of Unactivated Alkenes using CsOCF3 as a Trifluoromethoxide Source
inferred← citeshttps://doi.org/10.1002/ange.201902805openalex-snapshot
Carbonsäurefluoride in der Katalyse durch späte Übergangsmetalle
inferred← citeshttps://doi.org/10.1002/ange.202001015openalex-snapshot
Deoxyfluorination with CuF2: Enabled by Using a Lewis Base Activating Group
inferred← citeshttps://doi.org/10.1002/ange.202301343openalex-snapshot
Interaction between Divalent Copper Fluoride and Carboxamide Group Enabling Stereoretentive Fluorination of Tertiary Alkyl Halides
inferred← citeshttps://doi.org/10.1002/ange.202414933openalex-snapshot
Photocatalyzed Aryl C‐H Fluorocarbonylation with CF 2 Br 2
inferred← citeshttps://doi.org/10.1002/ange.202418738openalex-snapshot
π‐Lewis Base Activation of Carbonyls and Hexafluorobenzene
inferred← citeshttps://doi.org/10.1002/anie.201205260openalex-snapshot
Synthesis of Fluorinated Building Blocks by Transition‐Metal‐Mediated Hydrodefluorination Reactions
inferred← citeshttps://doi.org/10.1002/anie.201207356openalex-snapshot
Rhodium‐Catalyzed Enantioselective Nucleophilic Fluorination: Ring Opening of Oxabicyclic Alkenes
inferred← citeshttps://doi.org/10.1002/anie.201301097openalex-snapshot
Manganese‐Catalyzed Oxidative Benzylic C–H Fluorination by Fluoride Ions
inferred← citeshttps://doi.org/10.1002/anie.201301891openalex-snapshot
Copper‐Catalyzed Regioselective Fluorination of Allylic Halides
inferred← citeshttps://doi.org/10.1002/anie.201305106openalex-snapshot
Insertion of CS2 into Iridium–Fluorine Bonds
inferred← citeshttps://doi.org/10.1002/anie.201308071openalex-snapshot
Kinetic Resolution of Allyl Fluorides by Enantioselective Allylic Trifluoromethylation Based on Silicon‐Assisted CF Bond Cleavage
inferred← citeshttps://doi.org/10.1002/anie.201309535openalex-snapshot
Palladium‐Catalyzed Difluoroalkylation of Aryl Boronic Acids: A New Method for the Synthesis of Aryldifluoromethylated Phosphonates and Carboxylic Acid Derivatives
inferred← citeshttps://doi.org/10.1002/anie.201402238openalex-snapshot
Mild Copper‐Catalyzed Fluorination of Alkyl Triflates with Potassium Fluoride
inferred← citeshttps://doi.org/10.1002/anie.201404423openalex-snapshot
Mild and Versatile Nitrate‐Promoted CH Bond Fluorination
inferred← citeshttps://doi.org/10.1002/anie.201405653openalex-snapshot
Nickel‐Catalyzed Cross‐Coupling of Functionalized Difluoromethyl Bromides and Chlorides with Aryl Boronic Acids: A General Method for Difluoroalkylated Arenes
inferred← citeshttps://doi.org/10.1002/anie.201410288openalex-snapshot
Late‐Stage Fluorination: Fancy Novelty or Useful Tool?
inferred← citeshttps://doi.org/10.1002/anie.201410954openalex-snapshot
Condensed‐Phase, Halogen‐Bonded CF3I and C2F5I Adducts for Perfluoroalkylation Reactions
inferred← citeshttps://doi.org/10.1002/anie.201500399openalex-snapshot
Targeted Fluorination with the Fluoride Ion by Manganese‐Catalyzed Decarboxylation
inferred← citeshttps://doi.org/10.1002/anie.201502882openalex-snapshot
Facile Access to Fluoromethylated Arenes by Nickel‐Catalyzed Cross‐Coupling between Arylboronic Acids and Fluoromethyl Bromide
inferred← citeshttps://doi.org/10.1002/anie.201506882openalex-snapshot
Catalytic Nucleophilic Fluorination of Secondary and Tertiary Propargylic Electrophiles with a Copper–N‐Heterocyclic Carbene Complex
inferred← citeshttps://doi.org/10.1002/anie.201511321openalex-snapshot
Nickel‐Catalyzed Decarboxylative Difluoroalkylation of α,β‐Unsaturated Carboxylic Acids
inferred← citeshttps://doi.org/10.1002/anie.201603210openalex-snapshot
Asymmetric Desymmetrization via Metal‐Free C−F Bond Activation: Synthesis of 3,5‐Diaryl‐5‐fluoromethyloxazolidin‐2‐ones with Quaternary Carbon Centers
inferred← citeshttps://doi.org/10.1002/anie.201603426openalex-snapshot
Site‐Selective Tertiary Alkyl–Fluorine Bond Formation from α‐Bromoamides Using a Copper/CsF Catalyst System
inferred← citeshttps://doi.org/10.1002/anie.201610047openalex-snapshot
Nickel(0)‐Mediated Transformation of Tetrafluoroethylene and Vinylarenes into Fluorinated Cyclobutyl Compounds
inferred← citeshttps://doi.org/10.1002/anie.201708003openalex-snapshot
Transition‐Metal‐Free Catalytic Hydrodefluorination of Polyfluoroarenes by Concerted Nucleophilic Aromatic Substitution with a Hydrosilicate
inferred← citeshttps://doi.org/10.1002/anie.201708197openalex-snapshot
Selective Radical Fluorination of Tertiary Alkyl Halides at Room Temperature
inferred← citeshttps://doi.org/10.1002/anie.201801280openalex-snapshot
Benzylic Fluorination of Aza‐Heterocycles Induced by Single‐Electron Transfer to Selectfluor
inferred← citeshttps://doi.org/10.1002/anie.201808021openalex-snapshot
Selective C(sp 3 )−H and C(sp 2 )−H Fluorination of Alcohols Using Practical Auxiliaries
inferred← citeshttps://doi.org/10.1002/anie.201812927openalex-snapshot
Regioselective Vinylation of Remote Unactivated C(sp3)−H Bonds: Access to Complex Fluoroalkylated Alkenes
inferred← citeshttps://doi.org/10.1002/anie.201813591openalex-snapshot
Palladium(II)‐Catalyzed Enantioselective Aminotrifluoromethoxylation of Unactivated Alkenes using CsOCF 3 as a Trifluoromethoxide Source
inferred← citeshttps://doi.org/10.1002/anie.201902805openalex-snapshot
Acyl Fluorides in Late‐Transition‐Metal Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202001015openalex-snapshot
Deoxyfluorination with CuF 2 : Enabled by Using a Lewis Base Activating Group
inferred← citeshttps://doi.org/10.1002/anie.202301343openalex-snapshot
Interaction between Divalent Copper Fluoride and Carboxamide Group Enabling Stereoretentive Fluorination of Tertiary Alkyl Halides
inferred← citeshttps://doi.org/10.1002/anie.202414933openalex-snapshot
Photocatalyzed Aryl C‐H Fluorocarbonylation with CF 2 Br 2
inferred← citeshttps://doi.org/10.1002/anie.202418738openalex-snapshot
π‐Lewis Base Activation of Carbonyls and Hexafluorobenzene
inferred← citeshttps://doi.org/10.1002/asia.201400049openalex-snapshot
Asymmetric Decarboxylative 1,4‐Addition of Malonic Acid Half Thioesters to Vinyl Sulfones: Highly Enantioselective Synthesis of 3‐Monofluoromethyl‐3‐Arylpropanoic Esters
inferred← citeshttps://doi.org/10.1002/asia.201601036openalex-snapshot
Competition of Nucleophilic Aromatic Substitution, σ‐Bond Metathesis, and syn Hydrometalation in Titanium(III)‐Catalyzed Hydrodefluorination of Arenes
inferred← citeshttps://doi.org/10.1002/asia.202000059openalex-snapshot
Silver‐Catalyzed Decarboxylative Allylation of Difluoroarylacetic Acids with Allyl Sulfones in Water
inferred← citeshttps://doi.org/10.1002/asia.202001160openalex-snapshot
Utilization of Unsymmetric Diaryliodonium Salts in α‐Arylation of α‐Fluoroacetoacetamides
inferred← citeshttps://doi.org/10.1002/cctc.70833openalex-snapshot
Stereoselective Production of Fluorohydrins Biocatalyzed by an Alcohol Dehydrogenase From Pichia glucozyma
inferred← citeshttps://doi.org/10.1002/ceat.201500195openalex-snapshot
Photochemical Fluorination Reactions – A Promising Research Field for Continuous‐Flow Synthesis
inferred← citeshttps://doi.org/10.1002/chem.201201125openalex-snapshot
Titanium‐Catalyzed Vinylic and Allylic CF Bond Activation—Scope, Limitations and Mechanistic Insight
inferred← citeshttps://doi.org/10.1002/chem.201201576openalex-snapshot
Synthesis of 3‐Fluoropyrrolidines and 4‐Fluoropyrrolidin‐2‐ones from Allylic Fluorides
inferred← citeshttps://doi.org/10.1002/chem.201303385openalex-snapshot
Catalytic and Asymmetric Fluorolactonisations of Carboxylic Acids through Anion Phase Transfer
inferred← citeshttps://doi.org/10.1002/chem.201402282openalex-snapshot
Synthesis of Fluorinated Heteroaromatics through Formal Substitution of a Nitro Group by Fluorine under Transition‐Metal‐Free Conditions
inferred← citeshttps://doi.org/10.1002/chem.201402640openalex-snapshot
Elemental F2 with Transannular Dienes: Regioselectivities and Mechanisms
inferred← citeshttps://doi.org/10.1002/chem.201403141openalex-snapshot
Harnessing the ortho ‐Directing Ability of the Azetidine Ring for the Regioselective and Exhaustive Functionalization of Arenes
inferred← citeshttps://doi.org/10.1002/chem.201501811openalex-snapshot
Perfluoroalkyl and ‐aryl Zinc Ate Complexes: Generation, Reactivity, and Synthetic Application
inferred← citeshttps://doi.org/10.1002/chem.201502744openalex-snapshot
Ni‐Catalyzed Synthesis of Fluoroarenes via [2+2+2] Cycloaddition Involving α‐Fluorine Elimination
inferred← citeshttps://doi.org/10.1002/chem.201504749openalex-snapshot
A Fluorination/Aryl Migration/Cyclization Cascade for the Metal‐Free Synthesis of Fluoro‐Benzoxazepines
inferred← citeshttps://doi.org/10.1002/chem.201504838openalex-snapshot
Oxydifluoromethylation of Alkenes by Photoredox Catalysis: Simple Synthesis of CF 2 H‐Containing Alcohols
inferred← citeshttps://doi.org/10.1002/chem.201605336openalex-snapshot
Vicinal Difluoroalkylation and Aminosulfonylation of Alkynes under Photoinduced Conditions
inferred← citeshttps://doi.org/10.1002/chem.201700403openalex-snapshot
The Versatile Behavior of Platinum Alkyne Complexes towards XeF2: Formation of Fluorovinyl and Fluorido Complexes
inferred← citeshttps://doi.org/10.1002/chem.201706061openalex-snapshot
Organocatalytic C−F Bond Activation with Alanes
inferred← citeshttps://doi.org/10.1002/chem.201904727openalex-snapshot
Reaction of Vinyl Aziridines with Arynes: Synthesis of Benzazepines and Branched Allyl Fluorides
inferred← citeshttps://doi.org/10.1002/chem.201905040openalex-snapshot
Copper‐Mediated Fluorination of Aryl Trisiloxanes with Nucleophilic Fluoride
inferred← citeshttps://doi.org/10.1002/chem.202000081openalex-snapshot
Catalytic Asymmetric Fluorination of Copper Carbene Complexes: Preparative Advances and a Mechanistic Rationale
inferred← citeshttps://doi.org/10.1002/chem.202001627openalex-snapshot
A HF Loaded Lewis‐Acidic Aluminium Chlorofluoride for Hydrofluorination Reactions
inferred← citeshttps://doi.org/10.1002/chem.202004769openalex-snapshot
Silver‐Promoted Fluorination Reactions of α‐Bromoamides
inferred← citeshttps://doi.org/10.1002/chem.202101499openalex-snapshot
Bench‐Stable Electrophilic Fluorinating Reagents for Highly Selective Mono‐ and Difluorination of Silyl Enol Ethers
inferred← citeshttps://doi.org/10.1002/chem.202102451openalex-snapshot
Platinum Indolylphosphine Fluorido and Polyfluorido Complexes: An Interplay between Cyclometallation, Fluoride Migration, and Hydrogen Bonding
inferred← citeshttps://doi.org/10.1002/chem.202202768openalex-snapshot
Hydrogen Bonding in Platinum Indolylphosphine Polyfluorido and Fluorido Complexes
inferred← citeshttps://doi.org/10.1002/chem.202402339openalex-snapshot
N‐Heterocyclic Carbenes and N‐Heterocycles as Synthetic Reagents and Building Blocks
inferred← citeshttps://doi.org/10.1002/chem.202403298openalex-snapshot
Regio‐, Site‐ and Stereo‐Selective Aziridination of Conjugated Dienes Enabled by Palladium/Copper/Iodide/Oxygen Cooperation
inferred← citeshttps://doi.org/10.1002/chin.201226222openalex-snapshot
ChemInform Abstract: Transition Metal Catalysis and Nucleophilic Fluorination
inferred← citeshttps://doi.org/10.1002/cjoc.201800016openalex-snapshot
Decarboxylative Fluorination of Arylcarboxylic Acids Promoted by ortho‐Hydroxy and Amino Groups
inferred← citeshttps://doi.org/10.1002/cplu.201300214openalex-snapshot
Exploring Pathways for Activation of Carbon Monoxide by Palladium Iminophosphines
inferred← citeshttps://doi.org/10.1002/cssc.202401057openalex-snapshot
Protodefluorinated Selectfluor® Aggregatively Activates Selectfluor® for Efficient Radical C(sp3)−H Fluorination Reactions
inferred← citeshttps://doi.org/10.1002/ejic.202200668openalex-snapshot
Hydrogen and Halogen Bonding to Au(I) Fluorido Complexes
inferred← citeshttps://doi.org/10.1002/ejoc.201402097openalex-snapshot
Transition‐Metal‐Catalyzed Allylic Substitutions of Trichloroacetimidates
inferred← citeshttps://doi.org/10.1002/ejoc.201402587openalex-snapshot
An Efficient Method for Enhancing the Reactivity and Flexibility of [18F]Fluoride Towards Nucleophilic Substitution Using Tetraethylammonium Bicarbonate
inferred← citeshttps://doi.org/10.1002/ejoc.201403361openalex-snapshot
Highly Enantioselective Michael Addition of 2‐Fluoro‐1,3‐diketones to Nitroalkenes
inferred← citeshttps://doi.org/10.1002/ejoc.201500231openalex-snapshot
Advancements in Aminofluorination of Alkenes and Alkynes: Convenient Access to β‐Fluoroamines
inferred← citeshttps://doi.org/10.1002/ejoc.201500338openalex-snapshot
Synthesis of 5‐Fluorotriazoles by Silver‐Mediated Fluorination of 5‐Iodotriazoles
inferred← citeshttps://doi.org/10.1002/ejoc.201500370openalex-snapshot
Apparent Electrophilic Fluorination of 1,3‐Dicarbonyl Compounds Using Nucleophilic Fluoride Mediated by PhI(OAc)2
inferred← citeshttps://doi.org/10.1002/ejoc.201600954openalex-snapshot
Easy Access to Difluoromethylene‐Containing Arene Analogues through Palladium‐Catalysed C–H Olefination
inferred← citeshttps://doi.org/10.1002/ejoc.201900981openalex-snapshot
Synthesis of Fluorine‐Containing Molecular Entities Through Fluoride Ring Opening of Oxiranes and Aziridines
inferred← citeshttps://doi.org/10.1002/ejoc.201901717openalex-snapshot
Versatile Fluorinated Building Blocks by Stereoselective (Per)fluoroalkenylation of Ketones
inferred← citeshttps://doi.org/10.1002/ejoc.202100261openalex-snapshot
Recent Advances in Organic Synthesis Using Light‐Mediated N‐Heterocyclic Carbene Catalysis
inferred← citeshttps://doi.org/10.1002/ejoc.202301100openalex-snapshot
Reaction Mechanism and Origin of Stereoselectivity in the Fluorination and Trifluoromethylthiolation of 2‐Bromoamides with AgF and AgSCF3
inferred← citeshttps://doi.org/10.1002/ejoc.70461openalex-snapshot
Formation of C–F Bonds by Fluorination Using Visible Light
inferred← citeshttps://doi.org/10.1002/ijch.70027openalex-snapshot
Synthesis of Acyl Fluorides Using the Tribromoisocyanuric Acid (TBCA)/Triphenylphosphine/HF.Pyridine
inferred← citeshttps://doi.org/10.1002/nadc.201490011openalex-snapshot
Enantioselektive Fluorcyclisierungen
inferred← citeshttps://doi.org/10.1002/slct.202000189openalex-snapshot
An Efficient One‐Shot Metal‐Free Electrophilic Fluorination of 2‐Iminothiazolidine‐4‐one
inferred← citeshttps://doi.org/10.1002/slct.73799openalex-snapshot
Synthesis Aromatic Fluorides From Nitroarenes Via Nucleophilic Substitution With Organic Fluorination Agents or KF Recovered From Waste in Phosphorus Chemical Industry
inferred← citeshttps://doi.org/10.1002/tcr.202100231openalex-snapshot
Construction of Carbon‐Fluorine Bonds via Copper‐Catalyzed/‐Mediated Fluorination Reactions
inferred← citeshttps://doi.org/10.1002/tcr.202300140openalex-snapshot
Selective Synthesis of Monofluorinated Compounds Applying Amine/HF Reagents
inferred← citeshttps://doi.org/10.1002/tcr.202300143openalex-snapshot
Cross‐Coupling Reactions Enabled by Well‐Defined Ag(III) Compounds: Main Focus on Aromatic Fluorination and Trifluoromethylation
inferred← citeshttps://doi.org/10.1007/3418_2014_80openalex-snapshot
Visible-Light-Induced Redox Reactions by Ruthenium Photoredox Catalyst
inferred← citeshttps://doi.org/10.1007/978-3-030-18778-1_34openalex-snapshot
Studies of C–H Activation and Functionalization: Combined Computational and Experimental Efforts to Elucidate Mechanisms, Principles, and Catalysts
inferred← citeshttps://doi.org/10.1007/978-3-032-26476-3_18openalex-snapshot
Radiopharmaceutical Chemistry of Fluorine-18: Electrophilic Fluorinations
inferred← citeshttps://doi.org/10.1007/978-3-319-04346-3_1openalex-snapshot
Tactical Applications of Fluorine in Drug Design and Development
inferred← citeshttps://doi.org/10.1007/978-981-10-1855-8_27-1openalex-snapshot
Copper-Mediated Nucleophilic Fluorination for Preparing Alkyl Fluorides
inferred← citeshttps://doi.org/10.1007/978-981-10-1855-8_29-1openalex-snapshot
Transition Metal-Mediated Fluorination with Electrophilic/Nucleophilic Fluorinating Agents
inferred← citeshttps://doi.org/10.1007/978-981-10-3896-9_27openalex-snapshot
Copper-Mediated Nucleophilic Fluorination for Preparing Alkyl Fluorides
inferred← citeshttps://doi.org/10.1007/978-981-10-3896-9_29openalex-snapshot
Transition Metal-Mediated Fluorination with Electrophilic/Nucleophilic Fluorinating Agents
inferred← citeshttps://doi.org/10.1007/s00775-016-1414-3openalex-snapshot
Beyond ferryl-mediated hydroxylation: 40 years of the rebound mechanism and C–H activation
inferred← citeshttps://doi.org/10.1007/s10562-024-04860-2openalex-snapshot
Metal-Free Photoredox Catalysis for the S-Trifluoromethylation of Thiols
inferred← citeshttps://doi.org/10.1007/s11244-014-0259-7openalex-snapshot
Trifluoromethylation by Visible-Light-Driven Photoredox Catalysis
inferred← citeshttps://doi.org/10.1007/s11426-024-2240-5openalex-snapshot
Phase-transfer-shuttle generated in situ enables novel SN1-type fluorination of sulfonium ylide with hydrofluoric acid
inferred← citeshttps://doi.org/10.1007/s40242-015-4456-0openalex-snapshot
Difluoromethylation of 2-hydroxychalcones using sodium 2-chloro-2,2-difluoroacetate as difluoromethylating agent
inferred← citeshttps://doi.org/10.1007/s41061-016-0084-5openalex-snapshot
Palladium Catalyst Supported on Zeolite for Cross-coupling Reactions: An Overview of Recent Advances
inferred← citeshttps://doi.org/10.1007/s41061-024-00451-2openalex-snapshot
Transition-Metal Catalyzed Synthesis of Pyrimidines: Recent Advances, Mechanism, Scope and Future Perspectives
inferred← citeshttps://doi.org/10.1016/b978-0-08-097774-4.00128-5openalex-snapshot
Noble-Gas Chemistry
inferred← citeshttps://doi.org/10.1016/b978-0-12-812733-9.00001-5openalex-snapshot
Emerging fluorination methods in organic chemistry relevant for life science application
inferred← citeshttps://doi.org/10.1016/j.checat.2021.12.010openalex-snapshot
A photoredox-catalyzed approach for formal hydride abstraction to enable C –H functionalization with nucleophilic partners (F, C, O, N, and Br/Cl)
inferred← citeshttps://doi.org/10.1016/j.crci.2015.01.013openalex-snapshot
Sunlight-driven trifluoromethylation of olefinic substrates by photoredox catalysis: A green organic process
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2013.09.006openalex-snapshot
Co(salen)-mediated enantioselective radiofluorination of epoxides. Radiosynthesis of enantiomerically enriched [18F]F-MISO via kinetic resolution
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2014.06.025openalex-snapshot
Recent progress in transition-metal-catalyzed trifluoromethylation of olefins using electrophilic CF3 reagents
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2015.06.008openalex-snapshot
Pinpoint-fluorinated phenanthrene synthesis based on C F bond activation of difluoroalkenes
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2015.06.026openalex-snapshot
Chemically oxidative fluorination with fluoride ions
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2015.07.007openalex-snapshot
Review of recent advances in C F bond activation of aliphatic fluorides
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2015.07.020openalex-snapshot
Trifluoromethylation of aromatic alkenes by visible-light-driven photoredox catalysis: Direct conversion of alkenes to 3-trifluoromethyl-1-propenyl and 1,3-bis(trifluoromethyl)-1-propenyl derivatives
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2016.02.011openalex-snapshot
Quantification of hydrogen fluoride-based reagents using a bifunctional NMR internal standard
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2016.11.012openalex-snapshot
Nucleophilic monofluoroalkylation with fluorinated phosphonium salt toward carbonyl and imine compounds
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2016.12.017openalex-snapshot
Synthesis of trifluoromethyl moieties by late-stage copper (I) mediated nucleophilic fluorination
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2017.09.002openalex-snapshot
Pinpoint-fluorinated polycyclic aromatic hydrocarbons (F-PAHs): Syntheses of difluorinated subfamily and their properties
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2018.04.002openalex-snapshot
5-Exo-dig aminocylization/hydroxyfluorination of propargylic carbamates
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2019.109432openalex-snapshot
1,1-Bis(dimethylamino)-2,2-difluoroethene, a diverse building block for the preparation of difluoroalkyl molecules. Acylation and condensation reactions
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2020.109454openalex-snapshot
Chemoselective nucleophilic additions to perfluorocyclopentene: An efficient building block to highly fluorinated molecules
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2017.04.013openalex-snapshot
d8 Nickel and palladium difluorocarbenes derived from trifluoromethyl POCOP-type pincer complexes
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2017.07.009openalex-snapshot
Functionalized nitrogen ligands for palladium catalyzed cross-coupling reactions (part I)
inferred← citeshttps://doi.org/10.1016/j.molliq.2020.112819openalex-snapshot
Reaction evolution of a solvate fluoride ionic liquid induced fluorination process probed by Raman spectroscopy
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.146250openalex-snapshot
Studies on fluorinative difunctionalization of some β-amino acid derivatives and β-lactams with a cycloalkene framework
inferred← citeshttps://doi.org/10.1016/j.rechem.2022.100706openalex-snapshot
A method for the nucleophilic fluorination of 4-dimethylaminopyridine (DMAP) pyridinium salts
inferred← citeshttps://doi.org/10.1016/j.tet.2014.03.067openalex-snapshot
Efficient access to fluorinated homoallylic alcohols through an indium promoted fluoroallylation reaction
inferred← citeshttps://doi.org/10.1016/j.tet.2015.04.066openalex-snapshot
Rhodium-catalyzed benzylic fluorination of trichloroacetimidates
inferred← citeshttps://doi.org/10.1016/j.tet.2018.09.038openalex-snapshot
Catalyst-free fluorinative alkoxylation of alkenes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.07.134openalex-snapshot
Oxytrifluoromethylation of multiple bonds using copper catalyst under mild conditions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.03.082openalex-snapshot
A practical and straightforward access to fluorinated homoallylic alcohols in aqueous media
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.07.013openalex-snapshot
Biocatalyzed synthesis of both enantiopure fluoromisonidazole antipodes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.06.006openalex-snapshot
Review of recent advances in nucleophilic C–F bond-forming reactions at sp3 centers
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.03.028openalex-snapshot
Regio- and stereoselective synthesis of functionalized allylic fluorides via palladium-catalyzed three-component tandem carbofluorination of allenes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.09.010openalex-snapshot
Visible-light-mediated direct perfluoroalkylation and trifluoromethylation of free anilines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.01.044openalex-snapshot
Site selectivities in fluorination
inferred← citeshttps://doi.org/10.1021/acs.bioconjchem.5b00278openalex-snapshot
Novel Method for Radiolabeling and Dimerizing Thiolated Peptides Using 18F-Hexafluorobenzene
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00203openalex-snapshot
Fluorine and Gold: A Fruitful Partnership
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.1c02959openalex-snapshot
Synthesis, Reactivity, and Bonding of Gold(I) Fluorido–Phosphine Complexes
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.4c00400openalex-snapshot
Investigating the Mechanism of Aluminum Fluoride Chelation
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.5b02895openalex-snapshot
Synthesis, Bonding, and Reactivity of Vanadium(IV) Oxido–Fluorido Compounds with Neutral Chelate Ligands of the General Formula cis-[VIV(═O)(F)(LN–N)2]+
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02845openalex-snapshot
Nucleophilic Fluorination of Heteroaryl Chlorides and Aryl Triflates Enabled by Cooperative Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00388openalex-snapshot
Direct Deoxyfluorination of Alcohols with KF as the Fluorine Source
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00802openalex-snapshot
Regioselective C3-Fluoroalcoholation of Indoles with Heptafluoroisopropyl Iodide via Palladium-Catalyzed C(sp2)–C(sp3) Cross-Coupling in the Presence of O2
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02069openalex-snapshot
Fluorohydroxylation and Hydration Reactions of para-Quinone Methides Promoted by Selectfluor
inferred← citeshttps://doi.org/10.1021/acs.joc.3c01897openalex-snapshot
Late-Stage Diversification of Peptides via Pd-Catalyzed Site-Selective δ-C(sp2)-H Fluorination and Amination
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00709openalex-snapshot
PdII/CuI-Cocatalyzed Radical Arylation of gem-Difluoroalkenes Using Arylsulfonyl Chlorides
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02540openalex-snapshot
Electro-oxidative Deoxyfluorination of Arenes with NEt3·3HF
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00826openalex-snapshot
Mechanistic Study of Silver-Catalyzed Decarboxylative Fluorination
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02958openalex-snapshot
Cu(I)-Catalyzed Synthesis of Sulfenamides via Coupling of Carbamothioate/Thiourea Derivatives with Sulfonyl Azides
inferred← citeshttps://doi.org/10.1021/acs.joc.6b01334openalex-snapshot
Stereoselective Organocatalytic Synthesis of α,α-Difluoro-γ,γ-Disubstituted Butenals
inferred← citeshttps://doi.org/10.1021/acs.joc.6b01624openalex-snapshot
Theoretical Design and Calculation of a Crown Ether Phase-Transfer-Catalyst Scaffold for Nucleophilic Fluorination Merging Two Catalytic Concepts
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00036openalex-snapshot
A Systematic Evaluation of the N–F Bond Strength of Electrophilic N–F Reagents: Hints for Atomic Fluorine Donating Ability
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00927openalex-snapshot
Trifluoromethylation of Electron-Rich Alkenyl Iodides with Fluoroform-Derived “Ligandless” CuCF3
inferred← citeshttps://doi.org/10.1021/acs.joc.9b02001openalex-snapshot
“Ligandless” Pentafluoroethylation of Unactivated (Hetero)aryl and Alkenyl Halides Enabled by the Controlled Self-Condensation of TMSCF3-Derived CuCF3
inferred← citeshttps://doi.org/10.1021/acs.organomet.6b00908openalex-snapshot
Transition-Metal-Free Formation of C–E Bonds (E = C, N, O, S) and Formation of C–M Bonds (M = Mn, Mo) from N-Heterocyclic Carbene Mediated Fluoroalkene C–F Bond Activation
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03604openalex-snapshot
Multifunctional Crown-5-calix[4]arene-based Phase-Transfer Catalysts for Aromatic 18F-Fluorination
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c04087openalex-snapshot
Acyl Fluorides from Carboxylic Acids, Aldehydes, or Alcohols under Oxidative Fluorination
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00671openalex-snapshot
Late-Stage 18F/19F Isotopic Exchange for the Synthesis of 18F-Labeled Sulfamoyl Fluorides
showing the first 200 of 398 · page through all 398
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.