On the public citation graph
Scope of the Suzuki−Miyaura Cross-Coupling Reactions of Potassium Heteroaryltrifluoroborates
0 signed · 304 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known work and none has been retracted — and get a dated CiteStamped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/10.1002/1615-4169(200212)344:10<1146::aid-adsc1146>3.0.co;2-1openalex-snapshot
Convenient Approach to 3,4-Diarylisoxazoles Based on the Suzuki Cross-Coupling Reaction
inferredcites →https://doi.org/10.1002/9781118380208.ch4openalex-snapshot
Palladium in Heterocyclic Chemistry
inferredcites →https://doi.org/10.1002/9781119998372openalex-snapshot
Heterocycles in Life and Society
inferredcites →https://doi.org/10.1002/anie.200503479openalex-snapshot
A Versatile Method for Suzuki Cross‐Coupling Reactions of Nitrogen Heterocycles
inferredcites →https://doi.org/10.1002/anie.200600493openalex-snapshot
A Highly Active Catalyst for Suzuki–Miyaura Cross‐Coupling Reactions of Heteroaryl Compounds
inferredcites →https://doi.org/10.1002/anie.200703767openalex-snapshot
A Sydnone Cycloaddition Route to Pyrazole Boronic Esters
inferredcites →https://doi.org/10.1002/anie.200704162openalex-snapshot
Cyclic Triolborates: Air‐ and Water‐Stable Ate Complexes of Organoboronic Acids
inferredcites →https://doi.org/10.1002/anie.200801465openalex-snapshot
A General and Efficient Method for the Suzuki–Miyaura Coupling of 2‐Pyridyl Nucleophiles
inferredcites →https://doi.org/10.1002/chem.200501400openalex-snapshot
Microwave‐Assisted Suzuki Coupling Reactions with an Encapsulated Palladium Catalyst for Batch and Continuous‐Flow Transformations
inferredcites →https://doi.org/10.1002/chem.200701877openalex-snapshot
Highly Efficient Suzuki–Miyaura Coupling of Heterocyclic Substrates through Rational Reaction Design
inferredcites →https://doi.org/10.1002/ejoc.200300294openalex-snapshot
Potassium Trifluoro(organo)borates: New Perspectives in Organic Chemistry
inferredcites →https://doi.org/10.1002/ejoc.200500911openalex-snapshot
Palladium‐Catalysed Cross‐Coupling and Related Reactions Involving Pyrroles
inferredcites →https://doi.org/10.1002/ejoc.200600089openalex-snapshot
Cross‐Coupling Reactions on Azoles with Two and More Heteroatoms
inferredcites →https://doi.org/10.1002/ejoc.200701156openalex-snapshot
(Dimethoxy‐ and Dihalopyridyl)boronic Acids and Highly Functionalized Heteroarylpyridines by Suzuki Cross‐Coupling Reactions
inferredcites →https://doi.org/10.1002/jhet.5570130624openalex-snapshot
Etude des pK a et de la protodéboronation des acides furanneboroniques
inferredcites →https://doi.org/10.1002/jhet.5570270756openalex-snapshot
Synthesis of various 5‐substituted uracils
inferredcites →https://doi.org/10.1002/jhet.5570320410openalex-snapshot
Syntheses of various 5‐(bromoaryl)‐substituted uracils
inferredcites →https://doi.org/10.1007/s00217-001-0459-9openalex-snapshot
Comparison of potent odorants in a filtered coffee brew and in an instant coffee beverage by aroma extract dilution analysis (AEDA)
inferredcites →https://doi.org/10.1016/c2009-0-15932-9openalex-snapshot
Comprehensive Heterocyclic Chemistry
inferredcites →https://doi.org/10.1016/j.bmc.2008.01.010openalex-snapshot
11-(Pyridinylphenyl)steroids—A new class of mixed-profile progesterone agonists/antagonists
inferredcites →https://doi.org/10.1016/j.bmcl.2007.06.017openalex-snapshot
2-Aryl-N-acyl indole derivatives as liver X receptor (LXR) agonists
inferredcites →https://doi.org/10.1016/j.molcata.2007.01.011openalex-snapshot
Synthesis of biheteroaryl derivatives by tetraphosphine/palladium-catalysed Suzuki coupling of heteroaryl bromides with heteroarylboronic acids
inferredcites →https://doi.org/10.1016/j.tet.2005.02.070openalex-snapshot
2-Ethoxy-3-pyridylboronic acid: a versatile reagent for the synthesis of highly-functionalised 3-aryl/heteroaryl-pyridines via Suzuki cross-coupling reactions
inferredcites →https://doi.org/10.1016/j.tet.2005.05.015openalex-snapshot
Investigation of the scope of a [3+2] cycloaddition approach to isoxazole boronic esters
inferredcites →https://doi.org/10.1016/j.tet.2006.08.103openalex-snapshot
Pd(OAc)2/DABCO-catalyzed Suzuki–Miyaura cross-coupling reaction in DMF
inferredcites →https://doi.org/10.1016/j.tet.2007.01.061openalex-snapshot
Recent advances in organotrifluoroborates chemistry
inferredcites →https://doi.org/10.1016/j.tetlet.2003.11.068openalex-snapshot
The preparation of a stable 2-pyridylboronate and its reactivity in the Suzuki–Miyaura cross-coupling reaction
inferredcites →https://doi.org/10.1016/j.tetlet.2006.03.090openalex-snapshot
Regioselective Suzuki coupling of benzofuran or benzothiophene boronic acids and dibromo substituted naphthalenes: synthesis of a potent inhibitor of plasminogen activator inhibitor-1
inferredcites →https://doi.org/10.1016/j.tetlet.2006.04.125openalex-snapshot
Efficient and simple synthesis of 3-aryl-1H-pyrazoles
inferredcites →https://doi.org/10.1016/j.tetlet.2007.04.004openalex-snapshot
A facile synthetic route to new pyrazoloisoindolones
inferredcites →https://doi.org/10.1016/j.tetlet.2007.10.093openalex-snapshot
Synthesis of novel 7-substituted 5,6-dihydroindol-2-ones via a Suzuki–Miyaura cross-coupling strategy
inferredcites →https://doi.org/10.1016/s0022-328x(98)01055-9openalex-snapshot
Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles, 1995–1998
inferredcites →https://doi.org/10.1016/s0040-4020(02)00283-1openalex-snapshot
Synthesis of novel halopyridinylboronic acids and esters. Part 2: 2,4, or 5-Halopyridin-3-yl-boronic acids and esters
inferredcites →https://doi.org/10.1016/s0040-4020(02)00416-7openalex-snapshot
Synthesis of novel halopyridinylboronic acids and esters. Part 3: 2, or 3-Halopyridin-4-yl-boronic acids and esters
inferredcites →https://doi.org/10.1016/s0040-4039(01)01983-9openalex-snapshot
Synthesis and cross-coupling reactions of tetraalkylammonium organotrifluoroborate salts
inferredcites →https://doi.org/10.1021/ar050199qopenalex-snapshot
Organotrifluoroborates: Protected Boronic Acids That Expand the Versatility of the Suzuki Coupling Reaction
inferredcites →https://doi.org/10.1021/cr00039a007openalex-snapshot
Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
inferredcites →https://doi.org/10.1021/cr0505270openalex-snapshot
Practical Methodologies for the Synthesis of Indoles
inferredcites →https://doi.org/10.1021/cr0509758openalex-snapshot
Potassium Organotrifluoroborates: New Perspectives in Organic Synthesis
inferredcites →https://doi.org/10.1021/ja00405a035openalex-snapshot
Redox-photosensitized reactions. 7. Aromatic hydrocarbon-photosensitized electron-transfer reactions of furan, methylated furans, 1,1-diphenylethylene, and indene with p-dicyanobenzene
inferredcites →https://doi.org/10.1021/ja042491jopenalex-snapshot
Catalysts for Suzuki−Miyaura Coupling Processes: Scope and Studies of the Effect of Ligand Structure
inferredcites →https://doi.org/10.1021/ja068577popenalex-snapshot
Highly Efficient Monophosphine-Based Catalyst for the Palladium-Catalyzed Suzuki−Miyaura Reaction of Heteroaryl Halides and Heteroaryl Boronic Acids and Esters
inferredcites →https://doi.org/10.1021/jo00032a011openalex-snapshot
Synthesis of 3-arylpyrroles and 3-pyrrolylacetylenes by palladium-catalyzed coupling reactions
inferredcites →https://doi.org/10.1021/jo00115a016openalex-snapshot
Conversion of Arylboronic Acids into Potassium Aryltrifluoroborates: Convenient Precursors of Arylboron Difluoride Lewis Acids
inferredcites →https://doi.org/10.1021/jo0342368openalex-snapshot
Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions of Potassium Aryl- and Heteroaryltrifluoroborates
inferredcites →https://doi.org/10.1021/jo0402226openalex-snapshot
Palladium-Catalyzed Cross-Coupling Reactions of Pyridylboronic Acids with Heteroaryl Halides Bearing a Primary Amine Group: Synthesis of Highly Substituted Bipyridines and Pyrazinopyridines
inferredcites →https://doi.org/10.1021/jo048218hopenalex-snapshot
“Molecular Chameleons”. Design and Synthesis of a Second Series of Flexible Nucleosides
inferredcites →https://doi.org/10.1021/jo048334kopenalex-snapshot
A Concise Synthesis of a Novel Antiangiogenic Tyrosine Kinase Inhibitor
inferredcites →https://doi.org/10.1021/jo0491612openalex-snapshot
Arylboronic Acids and Arylpinacolboronate Esters in Suzuki Coupling Reactions Involving Indoles. Partner Role Swapping and Heterocycle Protection
inferredcites →https://doi.org/10.1021/jo060218popenalex-snapshot
Microwave-Assisted Preparation of Fused Bicyclic Heteroaryl Boronates: Application in One-Pot Suzuki Couplings
inferredcites →https://doi.org/10.1021/jo0608366openalex-snapshot
Palladium(0)-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions of Potassium Aryl- and Heteroaryltrifluoroborates with Alkenyl Bromides
inferredcites →https://doi.org/10.1021/jo070206jopenalex-snapshot
Fluorescent Pyrimidopyrimidoindole Nucleosides: Control of Photophysical Characterizations by Substituent Effects
inferredcites →https://doi.org/10.1021/jo8001886openalex-snapshot
Efficient Suzuki−Miyaura Coupling of (Hetero)aryl Chlorides with Thiophene- and Furanboronic Acids in Aqueousn-Butanol
inferredcites →https://doi.org/10.1021/jo991933kopenalex-snapshot
An Improved and Regiospecific Synthesis of trans-3,4-Dihydrodiol Metabolite of Benzo[b]naphtho[2,1-d]thiophene
inferredcites →https://doi.org/10.1021/ol0491686openalex-snapshot
Efficient Catalyst for the Suzuki−Miyaura Coupling of Potassium Aryl Trifluoroborates with Aryl Chlorides
inferredcites →https://doi.org/10.1021/ol060268gopenalex-snapshot
New Air-Stable Catalysts for General and Efficient Suzuki−Miyaura Cross-Coupling Reactions of Heteroaryl Chlorides
inferredcites →https://doi.org/10.1039/b103319kopenalex-snapshot
A regioselective cycloaddition route to isoxazoleboronic esters
inferredcites →https://doi.org/10.1039/b302767hopenalex-snapshot
5-Formyl-2-furylboronic acid as a versatile bifunctional reagent for the synthesis of π-extended heteroarylfuran systemsElectronic supplementary information (ESI) available: synthesis and characterisation data for 3–17. See http://www.rsc.org/suppdata/ob/b3/b302767h/
inferredcites →https://doi.org/10.1039/b314624nopenalex-snapshot
5-Pyrimidylboronic acid and 2-methoxy-5-pyrimidylboronic acid: new heteroarylpyrimidine derivatives via Suzuki cross-coupling reactions
inferredcites →https://doi.org/10.1039/b604586copenalex-snapshot
Heterocyclic terpenes: linear furano- and pyrroloterpenoids
inferredcites →https://doi.org/10.1039/b700433hopenalex-snapshot
Ruthenium half-sandwich complexes as protein kinase inhibitors: derivatization of the pyridocarbazole pharmacophore ligand
inferredcites →https://doi.org/10.1039/b712207aopenalex-snapshot
Ligand-free Pd/C-catalyzed Suzuki–Miyaura coupling reaction for the synthesis of heterobiaryl derivatives
inferredcites →https://doi.org/10.1055/s-2002-31914openalex-snapshot
Cross-coupling between 3-Pyridylmagnesium Chlorides and Heteroaromatic Halides
inferredcites →https://doi.org/10.1071/ch9651521openalex-snapshot
Protodeboronation of thiophenboronic acids
inferredcites →https://doi.org/10.1080/00397910701412828openalex-snapshot
Solvent‐Free, Palladium‐Catalyzed Suzuki–Miyaura Cross‐Couplings of Aryl Chlorides with Arylboronic Acids
inferredcites →https://doi.org/10.3987/com-92-6033openalex-snapshot
Synthesis of 5-Arylated Indoles via Palladium-catalyzed Cross-coupling Reaction of 5-Indolylboronic Acid with Aryl and Heteroaryl Halides
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.4753002openalex-extracted
Sunlight Induced C-H Arylation of Aromatic Heterocycles First Example of A3 and A2b Type Corroles as Photoredox Catalysts
inferred← citeshttps://doi.org/10.1002/047084289x.rn01372openalex-snapshot
5-Formyl-2-furanylboronic Acid
inferred← citeshttps://doi.org/10.1002/0471264180.or079.01openalex-snapshot
Cross‐Coupling Reactions of Organotrifluoroborate Salts
inferred← citeshttps://doi.org/10.1002/0471264180.or100.09openalex-snapshot
Suzuki–Miyaura Cross‐Coupling
inferred← citeshttps://doi.org/10.1002/0471264229.os092.28openalex-snapshot
Direct C7 Functionalization of Tryptophan. Synthesis of Methyl ( S )‐2‐(( tert ‐Butoxycarbonyl)amino)‐3‐(7‐(4,4,5,5‐tetramethyl‐1,3,2‐dioxaborolan‐2‐yl)‐1 H ‐indol‐3‐yl)propanoate
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0966openalex-snapshot
The Chemistry of Organotrifluoroborates
inferred← citeshttps://doi.org/10.1002/9781118662083.cot01-002openalex-snapshot
Formation of Alkanes and Arenes by Coupling Reactions
inferred← citeshttps://doi.org/10.1002/9783527639328.ch11openalex-snapshot
Organotrifluoroborates: Organoboron Reagents for the Twenty‐First Century
inferred← citeshttps://doi.org/10.1002/9783527655588.ch2openalex-snapshot
State‐of‐the‐Art in Metal‐Catalyzed Cross‐Coupling Reactions of Organoboron Compounds with Organic Electrophiles
inferred← citeshttps://doi.org/10.1002/adsc.200900638openalex-snapshot
Ligand‐Free and Heterogeneous Palladium on Carbon‐Catalyzed Hetero‐Suzuki–Miyaura Cross‐Coupling
inferred← citeshttps://doi.org/10.1002/adsc.200900683openalex-snapshot
New Synthesis of Furans: the Rhodium‐Catalysed Carbonylative Addition of Arylboronic Acids to Propargylic Alcohols/ Cyclisation Sequence
inferred← citeshttps://doi.org/10.1002/adsc.200900848openalex-snapshot
The 1,3‐Diaminobenzene‐Derived Aminophosphine Palladium Pincer Complex {C6H3[NHP(piperidinyl)2]2Pd(Cl)} – A Highly Active Suzuki–Miyaura Catalyst with Excellent Functional Group Tolerance
inferred← citeshttps://doi.org/10.1002/adsc.201000741openalex-snapshot
Rhodium or Palladium‐Catalyzed Cascade Aryl Addition/ Intramolecular Lactonization of Phthalaldehyde with Potassium Organotrifluoroborates to Access 3‐Arylphthalides
inferred← citeshttps://doi.org/10.1002/adsc.201000804openalex-snapshot
Palladium‐Catalyzed Carbonylative Suzuki Coupling of Benzyl Halides with Potassium Aryltrifluoroborates in Aqueous Media
inferred← citeshttps://doi.org/10.1002/adsc.201100226openalex-snapshot
Functionalization of the 3‐Position of Thiophene and Benzo[b]thiophene Moieties by Palladium‐Catalyzed CC Bond Forming Reactions using Diazonium Salts
inferred← citeshttps://doi.org/10.1002/adsc.201400520openalex-snapshot
Reusable, Highly Active Heterogeneous Palladium Catalyst by Convenient Self‐Encapsulation Cross‐Linking Polymerization for Multiple CarbonCarbon Cross‐Coupling Reactions at ppm to ppb Palladium Loadings
inferred← citeshttps://doi.org/10.1002/adsc.201500317openalex-snapshot
Diastereoselective Oxidative CN/CO and CN/CN Bond Formation Tandems Initiated by Visible Light: Synthesis of Fused N‐Arylindolines
inferred← citeshttps://doi.org/10.1002/ajoc.202000193openalex-snapshot
Synthetic Applications of Cyclopropene and Cyclopropenone: Recent Progress and Developments
inferred← citeshttps://doi.org/10.1002/ange.200904306openalex-snapshot
Organotrifluorborate und einfach koordinierte Palladiumkomplexe als Katalysatoren – die perfekte Kombination für die Suzuki‐Miyaura‐Kupplung
inferred← citeshttps://doi.org/10.1002/ange.200905897openalex-snapshot
Four‐Component Synthesis of Fully Substituted 1,2,4‐Triazoles
inferred← citeshttps://doi.org/10.1002/ange.201001522openalex-snapshot
Aryl Trifluoroborates in Suzuki–Miyaura Coupling: The Roles of Endogenous Aryl Boronic Acid and Fluoride
inferred← citeshttps://doi.org/10.1002/ange.201108608openalex-snapshot
A General Solution for the 2‐Pyridyl Problem
inferred← citeshttps://doi.org/10.1002/ange.201510027openalex-snapshot
Synthesis and Utility of Dihydropyridine Boronic Esters
inferred← citeshttps://doi.org/10.1002/ange.201712019openalex-snapshot
Effiziente Synthese von arylierten Furanen durch sequentielle Rhodium‐katalysierte Arylierung und Cycloisomerisierung von Cyclopropenen
inferred← citeshttps://doi.org/10.1002/ange.202010631openalex-snapshot
The 2‐Pyridyl Problem: Challenging Nucleophiles in Cross‐Coupling Arylations
inferred← citeshttps://doi.org/10.1002/ange.202512496openalex-snapshot
General Base‐Free Suzuki‐Miyaura Cross‐Coupling Reaction via Electrophilic Substitution Transmetalation
inferred← citeshttps://doi.org/10.1002/anie.200904306openalex-snapshot
Organotrifluoroborates and Monocoordinated Palladium Complexes as Catalysts—A Perfect Combination for Suzuki–Miyaura Coupling
inferred← citeshttps://doi.org/10.1002/anie.200905897openalex-snapshot
Four‐Component Synthesis of Fully Substituted 1,2,4‐Triazoles
inferred← citeshttps://doi.org/10.1002/anie.201001522openalex-snapshot
Aryl Trifluoroborates in Suzuki–Miyaura Coupling: The Roles of Endogenous Aryl Boronic Acid and Fluoride
inferred← citeshttps://doi.org/10.1002/anie.201108608openalex-snapshot
A General Solution for the 2‐Pyridyl Problem
inferred← citeshttps://doi.org/10.1002/anie.201510027openalex-snapshot
Synthesis and Utility of Dihydropyridine Boronic Esters
inferred← citeshttps://doi.org/10.1002/anie.201712019openalex-snapshot
Efficient Synthesis of Arylated Furans by a Sequential Rh‐Catalyzed Arylation and Cycloisomerization of Cyclopropenes
inferred← citeshttps://doi.org/10.1002/anie.202010631openalex-snapshot
The 2‐Pyridyl Problem: Challenging Nucleophiles in Cross‐Coupling Arylations
inferred← citeshttps://doi.org/10.1002/anie.202512496openalex-snapshot
General Base‐Free Suzuki‐Miyaura Cross‐Coupling Reaction via Electrophilic Substitution Transmetalation
inferred← citeshttps://doi.org/10.1002/aoc.2965openalex-snapshot
Tetraphosphine/palladium‐catalyzed Suzuki–Miyaura coupling of heteroaryl halides with 3‐pyridine‐ and 3‐thiopheneboronic acid: an efficient catalyst for the formation of biheteroaryls
inferred← citeshttps://doi.org/10.1002/aoc.3290openalex-snapshot
Palladium supported on silica–chitosan hybrid material (Pd‐CS@SiO 2 ) for Suzuki–Miyaura and Mizoroki–Heck cross‐coupling reactions
inferred← citeshttps://doi.org/10.1002/aoc.3504openalex-snapshot
Desulfonative pd‐catalyzed coupling of aryl trifluoroborates with arylsulfonyl chlorides
inferred← citeshttps://doi.org/10.1002/aoc.3970openalex-snapshot
Pd‐catalyzed Desulfitative reaction of Aryltrifluoroborates with sodium Arenesulfinates in water
inferred← citeshttps://doi.org/10.1002/aoc.6653openalex-snapshot
Suzuki–Miyaura arylation of 2,3‐, 2,4‐, 2,5‐, and 3,4‐dibromothiophenes
inferred← citeshttps://doi.org/10.1002/asia.201000589openalex-snapshot
Rhodium‐Catalyzed 1,4‐Addition of Lithium 2‐Furyltriolborates to Unsaturated Ketones and Esters for Enantioselective Synthesis of γ‐Oxo‐Carboxylic Acids By Oxidation of the Furyl Ring with Ozone
inferred← citeshttps://doi.org/10.1002/asia.201403359openalex-snapshot
The Regioselective Homocoupling of meta‐Hydroxypyridines with Hypervalent Iodine(III)
inferred← citeshttps://doi.org/10.1002/cctc.201301077openalex-snapshot
Regiocontroled Palladium‐Catalysed Direct Arylation at Carbon C2 of Benzofurans using Benzenesulfonyl Chlorides as the Coupling Partners
inferred← citeshttps://doi.org/10.1002/chem.201601584openalex-snapshot
Modular Construction of Fluoroarenes from a New Difluorinated Building Block by Cross‐Coupling/Electrocyclisation/Dehydrofluorination Reactions
inferred← citeshttps://doi.org/10.1002/chem.201702338openalex-snapshot
Direct C2‐Functionalization of Indoles Triggered by the Generation of Iminium Species from Indole and Sulfonium Salt
inferred← citeshttps://doi.org/10.1002/chin.200923099openalex-snapshot
ChemInform Abstract: Scope of the Suzuki—Miyaura Cross‐Coupling Reactions of Potassium Heteroaryltrifluoroborates.
inferred← citeshttps://doi.org/10.1002/cptc.201800125openalex-snapshot
Flow Photochemistry of Azosulfones: Application of “Sunflow” Reactors
inferred← citeshttps://doi.org/10.1002/cssc.201801382openalex-snapshot
Ligand‐Free Bioinspired Suzuki–Miyaura Coupling Reactions using Aryltrifluoroborates as Effective Partners in Deep Eutectic Solvents
inferred← citeshttps://doi.org/10.1002/ejic.201800045openalex-snapshot
Homo‐ and Heterodinuclear Iron Clathrochelate Complexes with Functional Groups in the Ligand Periphery
inferred← citeshttps://doi.org/10.1002/ejoc.200900309openalex-snapshot
Ligand‐Free‐Palladium‐Catalyzed Direct 4‐Arylation of Isoxazoles Using Aryl Bromides
inferred← citeshttps://doi.org/10.1002/ejoc.200900677openalex-snapshot
Microwave‐Assisted Palladium‐Catalyzed Heterogeneous Vinylation of 2(1H)‐Pyridones
inferred← citeshttps://doi.org/10.1002/ejoc.201101102openalex-snapshot
Methyl 2‐Furoate: An Alternative Reagent to Furan for Palladium‐Catalysed Direct Arylation
inferred← citeshttps://doi.org/10.1002/ejoc.201200657openalex-snapshot
Total Synthesis of Calothrixins A and B by Palladium‐Catalyzed Tandem Cyclization/Cross‐Coupling Reaction of Indolylborate
inferred← citeshttps://doi.org/10.1002/ejoc.201200918openalex-snapshot
Room‐Temperature Suzuki–Miyaura Coupling of Heteroaryl Chlorides and Tosylates
inferred← citeshttps://doi.org/10.1002/ejoc.201201314openalex-snapshot
Pd‐Catalyzed Tandem Chemoselective Synthesis of 2‐Arylbenzofurans using Threefold Arylating Triarylbismuth Reagents
inferred← citeshttps://doi.org/10.1002/ejoc.201201720openalex-snapshot
Organogold(I) Phosphanes in Palladium‐Catalyzed Cross‐Coupling Reactions in Aqueous Media
inferred← citeshttps://doi.org/10.1002/ejoc.201300334openalex-snapshot
An Aerobic and Very Fast Pd/C‐Catalyzed Ligand‐Free and Aqueous Suzuki Reaction Under Mild Conditions
inferred← citeshttps://doi.org/10.1002/ejoc.201300743openalex-snapshot
Iron‐Catalyzed Direct C–H Arylation of Heterocycles and Quinones with Arylboronic Acids
inferred← citeshttps://doi.org/10.1002/ejoc.201301084openalex-snapshot
Modular Hemisyntheses of Boronato‐ and Trifluoroborato‐Substituted L ‐NHBoc Amino Acid and Peptide Derivatives
inferred← citeshttps://doi.org/10.1002/ejoc.201402881openalex-snapshot
Suzuki–Miyaura Coupling of Aryl Chlorides with Arylboronic Acids Using the Morpholine–NiCl2 Catalyst System
inferred← citeshttps://doi.org/10.1002/ejoc.201402915openalex-snapshot
General Suzuki Coupling of Heteroaryl Bromides by Using Tri‐ tert ‐butylphosphine as a Supporting Ligand
inferred← citeshttps://doi.org/10.1002/ejoc.201500006openalex-snapshot
Visible‐Light‐Photocatalyzed Metal‐Free C–H Heteroarylation of Heteroarenes at Room Temperature: A Sustainable Synthesis of Biheteroaryls
inferred← citeshttps://doi.org/10.1002/ejoc.201600056openalex-snapshot
α‐Phosphonovinyl Arylsulfonates: An Attractive Partner for the Synthesis of α‐Substituted Vinylphosphonates through Palladium‐Catalyzed Suzuki Reactions
inferred← citeshttps://doi.org/10.1002/ejoc.201600199openalex-snapshot
Biaryl Ketones by Suzuki–Miyaura Cross‐Coupling of Organotrifluoroborates and Acyl Chlorides
inferred← citeshttps://doi.org/10.1002/ejoc.201701241openalex-snapshot
A Zwitterionic Palladium(II) Complex as a Precatalyst for Neat‐Water‐Mediated Cross‐Coupling Reactions of Heteroaryl, Benzyl, and Aryl Acid Chlorides with Organoboron Reagents
inferred← citeshttps://doi.org/10.1002/ejoc.201801173openalex-snapshot
Transition‐Metal‐Free Approach for the Direct Arylation of Thiophene: Experimental and Theoretical Investigations towards the (Het)‐Aryne Route
inferred← citeshttps://doi.org/10.1002/ejoc.201901000openalex-snapshot
Formation of 8‐Hydroxyphenanthridines by Microwave‐Mediated IMDAF Reactions; Synthesis Directed towards Lycorine Alkaloids
inferred← citeshttps://doi.org/10.1002/ijch.201000074openalex-snapshot
The Slow‐Release Strategy in Suzuki–Miyaura Coupling
inferred← citeshttps://doi.org/10.1002/pola.28682openalex-snapshot
Use of N‐methyliminodiacetic acid boronate esters in suzuki‐miyaura cross‐coupling polymerizations of triarylamine and fluorene monomers
inferred← citeshttps://doi.org/10.1007/7081_2012_82openalex-snapshot
Metalation of Pyrazoles and Indazoles
inferred← citeshttps://doi.org/10.1007/7081_2012_93openalex-snapshot
Other Stoichiometric Metalation Reactions on Pyrimidine and Quinazoline
inferred← citeshttps://doi.org/10.1007/7081_2014_138openalex-snapshot
Metal Catalyzed Cross-Coupling Reactions in the Decoration of Pyrimidine, Pyridazine, and Pyrazine
inferred← citeshttps://doi.org/10.1007/978-3-319-01134-9_3openalex-snapshot
Organotrifluoroborate Coupling
inferred← citeshttps://doi.org/10.1007/s10593-014-1443-1openalex-snapshot
An Effective Activation of Palladium Phosphine Complexes in Aqueous Phase Reactions of Hetero-Aromatic Boronic Acids with Aryl Halides
inferred← citeshttps://doi.org/10.1007/s10593-019-02492-8openalex-snapshot
Effective bimetallic composite catalysts for the synthesis of arylated furans and thiophenes in aqueous media
inferred← citeshttps://doi.org/10.1007/s11172-016-1306-2openalex-snapshot
Functionalized isoxazole and isothiazole ligands: design, synthesis, palladium complexes, homogeneous and heterogeneous catalysis in aqueous media
inferred← citeshttps://doi.org/10.1007/s12039-023-02142-9openalex-snapshot
Synthesis and structural characterization of unsymmetrical Schiff base 2-(1-(2-aminophenylimino)ethyl)phenol (LH3) and its Pd(II) complex [Pd3(LH)3]: catalysis of Suzuki–Miyaura cross-coupling reaction
inferred← citeshttps://doi.org/10.1016/b978-0-08-096805-6.00005-xopenalex-snapshot
Five-Membered Ring Systems
inferred← citeshttps://doi.org/10.1016/b978-0-12-396530-1.00004-8openalex-snapshot
Recent Advances in the C2 and C3 Regioselective Direct Arylation of Indoles
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.14773-0openalex-snapshot
Furans and Their Benzo Derivatives: Reactivity
inferred← citeshttps://doi.org/10.1016/b978-0-12-818655-8.00041-xopenalex-snapshot
Pyrimidines and Their Benzo Derivatives
inferred← citeshttps://doi.org/10.1016/j.apcata.2014.10.009openalex-snapshot
Heterogeneous palladium catalyst constructed with cross-linked hyperbranched poly(phenylacetylene) as polymer support: A reusable highly active ppm-level catalyst for multiple cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.bmc.2018.02.017openalex-snapshot
Pharmacophore requirements for HIV-1 reverse transcriptase inhibitors that selectively “Freeze” the pre-translocated complex during the polymerization catalytic cycle
inferred← citeshttps://doi.org/10.1016/j.catcom.2015.05.025openalex-snapshot
Palladium-catalyzed efficient Suzuki–Miyaura reaction of potassium aryltrifluoroborates in water
inferred← citeshttps://doi.org/10.1016/j.ejmech.2023.115894openalex-snapshot
Covalent and noncovalent strategies for targeting Lys102 in HIV-1 reverse transcriptase
inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2023.112275openalex-snapshot
Pd/Cu-catalyzed sonogashira cross-coupling polycondensation: A promising approach for synthesizing conjugated polymers with useful applications
inferred← citeshttps://doi.org/10.1016/j.jcat.2024.115635openalex-snapshot
Suzuki-Miyaura Cross-Coupling using convenient and accessible Nickelocene/Phosphine precatalyst
inferred← citeshttps://doi.org/10.1016/j.jcat.2024.115705openalex-snapshot
Sunlight induced C-H arylation of aromatic heterocycles: First example of A3 and A2B type corroles as photoredox catalysts
inferred← citeshttps://doi.org/10.1016/j.mcat.2020.111283openalex-snapshot
Synthesis, characterization and catalytic application of Bi2S3 microspheres for Suzuki-Miyaura cross-coupling reaction and chemoselective ring opening of epoxides
inferred← citeshttps://doi.org/10.1016/j.polymer.2012.11.083openalex-snapshot
A new precursor for conducting polymer-based brush interfaces with electroactivity in aqueous solution
inferred← citeshttps://doi.org/10.1016/j.tet.2009.10.015openalex-snapshot
Recent advances in the synthesis of (hetero)aryl-substituted heteroarenes via transition metal-catalysed direct (hetero)arylation of heteroarene C–H bonds with aryl halides or pseudohalides, diaryliodonium salts, and potassium aryltrifluoroborates
inferred← citeshttps://doi.org/10.1016/j.tet.2010.02.061openalex-snapshot
2-Pyridyl and 3-pyridylzinc bromides: direct preparation and coupling reaction
inferred← citeshttps://doi.org/10.1016/j.tet.2010.09.027openalex-snapshot
Palladium on charcoal-catalyzed ligand-free Stille coupling
inferred← citeshttps://doi.org/10.1016/j.tet.2011.05.031openalex-snapshot
CuI-catalyzed Suzuki coupling reaction of organoboronic acids with alkynyl bromides
inferred← citeshttps://doi.org/10.1016/j.tet.2011.10.057openalex-snapshot
Suzuki–Miyaura cross-coupling reaction of aryl and heteroaryl pinacol boronates for the synthesis of 2-substituted pyrimidines
inferred← citeshttps://doi.org/10.1016/j.tet.2011.12.036openalex-snapshot
Palladium-catalyzed Suzuki–Miyaura cross-coupling reaction of potassium 2-pyridyl trifluoroborate with aryl (heteroaryl) halides
inferred← citeshttps://doi.org/10.1016/j.tet.2013.09.010openalex-snapshot
A simple catalytic system based on PdCl2(CH3CN)2 in water for cross-coupling reactions using diazonium salts
inferred← citeshttps://doi.org/10.1016/j.tet.2015.04.026openalex-snapshot
A modified procedure for the palladium catalyzed borylation/Suzuki-Miyaura cross-coupling of aryl and heteroaryl halides utilizing bis-boronic acid
inferred← citeshttps://doi.org/10.1016/j.tet.2015.04.041openalex-snapshot
In situ-generated nano-palladium-catalyzed ligand-free Suzuki–Miyaura reaction of potassium aryltrifluoroborates at room temperature
inferred← citeshttps://doi.org/10.1016/j.tet.2020.130982openalex-snapshot
Straightforward convergent access to 2-arylated polysubstituted benzothiazoles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.03.155openalex-snapshot
Palladium-catalysed direct 3- or 4-arylation of thiophene derivatives using aryl bromides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.07.008openalex-snapshot
Synthesis of 3-aryl-4-chalcogen-2H-benzopyrans from 3-iodo-4-chalcogen-2H-benzopyrans using a Suzuki cross-coupling
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.09.008openalex-snapshot
Thermal and microwave hydrolysis of organotrifluoroborates mediated by alumina
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.10.087openalex-snapshot
Studies of microwave-enhanced Suzuki–Miyaura vinylation of electron-rich sterically hindered substrates utilizing potassium vinyltrifluoroborate
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.12.102openalex-snapshot
Silver-catalyzed cascade reaction of o-aminoaryl compounds with alkynes: an aniline mediated synthesis of 2-substituted quinolines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.03.059openalex-snapshot
Palladium-catalyzed cross-couplings of functionalized 2-bromobenzofurans for atom-economic synthesis of 2-arylbenzofurans using triarylbismuth reagents
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.11.047openalex-snapshot
The synthesis of novel pyrrololactams and their boronate ester derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.01.014openalex-snapshot
Synthesis of 2-arylindoles by Suzuki coupling reaction of 3-bromoindoles with hindered benzoboronic acids
inferred← citeshttps://doi.org/10.1016/s0959-6380(11)22001-4openalex-snapshot
Recent Advances in the C-2 Regioselective Direct Arylation of Indoles
inferred← citeshttps://doi.org/10.1016/s0959-6380(11)22005-1openalex-snapshot
Five-Membered Ring Systems
inferred← citeshttps://doi.org/10.1016/s0959-6380(11)22012-9openalex-snapshot
Six-Membered Ring Systems: Pyridines and Benzo Derivatives
inferred← citeshttps://doi.org/10.1021/acs.accounts.7b00514openalex-snapshot
Ambiphilic Molecules: From Organometallic Curiosity to Metal-Free Catalysts
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5c01220openalex-snapshot
Solvent Sustainability in Drug Discovery: Where Are We Now, and How Can We Improve?
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.7b01869openalex-snapshot
Repurposing a Library of Human Cathepsin L Ligands: Identification of Macrocyclic Lactams as Potent Rhodesain andTrypanosoma bruceiInhibitors
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.9b00663openalex-snapshot
Effect of Modifier Structure on the Activation of Leukotriene A4 Hydrolase Aminopeptidase Activity
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00178openalex-snapshot
Chemoselective Rhodium-Catalyzed Borylation of Bromoiodoarenes Under Mild Conditions
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01065openalex-snapshot
Transition-Metal-Free Borylation of Aryl Bromide Using a Simple Diboron Source
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02474openalex-snapshot
Convergent Synthesis of Fluoroalkenes Using a Dual-Reactive Unit
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00981openalex-snapshot
Organotrifluoroborates: Another Branch of the Mighty Oak
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02551openalex-snapshot
C–H-Activated Direct Arylation of Strong Benzothiadiazole and Quinoxaline-Based Electron Acceptors
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02662openalex-snapshot
Modular Approaches to Diversified Soft Lewis Basic Complexants through Suzuki–Miyaura Cross-Coupling of Bromoheteroarenes with Organotrifluoroborates
inferred← citeshttps://doi.org/10.1021/acs.joc.5c00319openalex-snapshot
Bichromophoric Ruthenium Complexes for Photocatalyzed Late-Stage Synthesis of Trifluoromethylated Indolizines
inferred← citeshttps://doi.org/10.1021/acs.joc.6b01619openalex-snapshot
Wavelength Selective Generation of Aryl Radicals and Aryl Cations for Metal-Free Photoarylations
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02534openalex-snapshot
Total Synthesis and Biological Evaluation of Hybrubin A
inferred← citeshttps://doi.org/10.1021/acs.joc.7b01711openalex-snapshot
Bulky Yet Flexible Pd-PEPPSI-IPentAn for the Synthesis of Sterically Hindered Biaryls in Air
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02623openalex-snapshot
One-Pot Reaction between N-Tosylhydrazones and 2-Nitrobenzyl Bromide: Route to NH-Free C2-Arylindoles
inferred← citeshttps://doi.org/10.1021/acs.oprd.8b00006openalex-snapshot
Development of Flexible and Scalable Routes to Two Phosphatidinylinositol-3-kinase Delta Inhibitors via a Common Intermediate Approach
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c03379openalex-snapshot
Synthesis of Bis-heteroaryls Using Grignard Reagents and Pyridylsulfonium Salts
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01750openalex-snapshot
Toward Efficient Nucleophilic Azaborine Building Blocks for the Synthesis of B–N Naphthyl (Hetero)arylmethane Isosteres
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02711openalex-snapshot
Lanthanide(III)-Catalyzed Synthesis of trans-Diaminocyclopentenones from Substituted Furfurals and Secondary Amines via a Domino Ring-Opening/4π-Electrocyclization Pathway
inferred← citeshttps://doi.org/10.1021/acsaem.1c01872openalex-snapshot
Microwave-Assisted Synthesis of Non-Fullerene Acceptors and Their Photovoltaic Studies for High-Performance Organic Solar Cells
inferred← citeshttps://doi.org/10.1021/acscatal.9b04353openalex-snapshot
Potassium Trimethylsilanolate Enables Rapid, Homogeneous Suzuki−Miyaura Cross-Coupling of Boronic Esters
inferred← citeshttps://doi.org/10.1021/acsomega.0c03415openalex-snapshot
Ligand Steric Effects of α-Diimine Nickel(II) and Palladium(II) Complexes in the Suzuki–Miyaura Cross-Coupling Reaction
inferred← citeshttps://doi.org/10.1021/ja1073799openalex-snapshot
A New Palladium Precatalyst Allows for the Fast Suzuki−Miyaura Coupling Reactions of Unstable Polyfluorophenyl and 2-Heteroaryl Boronic Acids
inferred← citeshttps://doi.org/10.1021/ja201485popenalex-snapshot
High-Performance Electron-Transporting Polymers Derived from a Heteroaryl Bis(trifluoroborate)
inferred← citeshttps://doi.org/10.1021/ja300236kopenalex-snapshot
Organotrifluoroborate Hydrolysis: Boronic Acid Release Mechanism and an Acid–Base Paradox in Cross-Coupling
inferred← citeshttps://doi.org/10.1021/ja901416popenalex-snapshot
A General Solution for Unstable Boronic Acids: Slow-Release Cross-Coupling from Air-Stable MIDA Boronates
inferred← citeshttps://doi.org/10.1021/jacs.1c06419openalex-snapshot
Heteroaryl–Heteroaryl, Suzuki–Miyaura, Anhydrous Cross-Coupling Reactions Enabled by Trimethyl Borate
inferred← citeshttps://doi.org/10.1021/jacs.6b03283openalex-snapshot
Protodeboronation of Heteroaromatic, Vinyl, and Cyclopropyl Boronic Acids: pH–Rate Profiles, Autocatalysis, and Disproportionation
inferred← citeshttps://doi.org/10.1021/jacs.9b08504openalex-snapshot
Nonsymmetrical Bis-Azine Biaryls from Chloroazines: A Strategy Using Phosphorus Ligand-Coupling
inferred← citeshttps://doi.org/10.1021/jm200640vopenalex-snapshot
3,5-Dimethylisoxazoles Act As Acetyl-lysine-mimetic Bromodomain Ligands
inferred← citeshttps://doi.org/10.1021/jm300915bopenalex-snapshot
Progress in the Development and Application of Small Molecule Inhibitors of Bromodomain–Acetyl-lysine Interactions
inferred← citeshttps://doi.org/10.1021/jm4018948openalex-snapshot
Synthesis, Cytostatic, Antimicrobial, and Anti-HCV Activity of 6-Substituted 7-(Het)aryl-7-deazapurine Ribonucleosides
inferred← citeshttps://doi.org/10.1021/jo1004058openalex-snapshot
Synthesis of an Acyltrifluoroborate and Its Fusion with Azides To Form Amides
inferred← citeshttps://doi.org/10.1021/jo100846topenalex-snapshot
A General Palladium Catalyst System for Suzuki−Miyaura Coupling of Potassium Aryltrifluoroborates and Aryl Mesylates
inferred← citeshttps://doi.org/10.1021/jo1014504openalex-snapshot
Divergent Route to Access Structurally Diverse 4-Quinolones via Mono or Sequential Cross-Couplings
inferred← citeshttps://doi.org/10.1021/jo1018969openalex-snapshot
Palladium-Catalyzed Indole, Pyrrole, and Furan Arylation by Aryl Chlorides
inferred← citeshttps://doi.org/10.1021/jo102208dopenalex-snapshot
Oxidation of Organotrifluoroborates via Oxone
inferred← citeshttps://doi.org/10.1021/jo2001066openalex-snapshot
Reinvestigation of Aminomethyltrifluoroborates and Their Application in Suzuki−Miyaura Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1021/jo201081vopenalex-snapshot
CuI/TMEDA-Catalyzed Annulation of 2-Bromo Alkynylbenzenes with Na2S: Synthesis of Benzo[b]thiophenes
inferred← citeshttps://doi.org/10.1021/jo201313aopenalex-snapshot
Metal-Free Chlorodeboronation of Organotrifluoroborates
inferred← citeshttps://doi.org/10.1021/jo201317topenalex-snapshot
Selective Mono- to Perarylations of Tetrabromothiophene by a Cyclobutene-1,2-diylbisimidazolium Preligand
inferred← citeshttps://doi.org/10.1021/jo201973topenalex-snapshot
Regioselective Synthesis and Slow-Release Suzuki–Miyaura Cross-Coupling of MIDA Boronate-Functionalized Isoxazoles and Triazoles
inferred← citeshttps://doi.org/10.1021/jo300551mopenalex-snapshot
Nitrosation of Aryl and Heteroaryltrifluoroborates with Nitrosonium Tetrafluoroborate
inferred← citeshttps://doi.org/10.1021/jo3011705openalex-snapshot
Suzuki–Miyaura Coupling Reactions of Iodo(difluoroenol) Derivatives, Fluorinated Building Blocks Accessible at Near-Ambient Temperatures
inferred← citeshttps://doi.org/10.1021/jo400433mopenalex-snapshot
Palladium-Catalyzed Addition of Potassium Aryltrifluoroborates to Aliphatic Nitriles: Synthesis of Alkyl Aryl Ketones, Diketone Compounds, and 2-Arylbenzo[b]furans
inferred← citeshttps://doi.org/10.1021/jo401104yopenalex-snapshot
Nickel-Catalyzed Borylation of Halides and Pseudohalides with Tetrahydroxydiboron [B 2 (OH) 4 ]
inferred← citeshttps://doi.org/10.1021/jo4024123openalex-snapshot
Synthesis of Heteroaryl Compounds through Cross-Coupling Reaction of Aryl Bromides or Benzyl Halides with Thienyl and Pyridyl Aluminum Reagents
inferred← citeshttps://doi.org/10.1021/jo500840sopenalex-snapshot
[Bmim]PF6-Promoted Ligandless Suzuki–Miyaura Coupling Reaction of Potassium Aryltrifluoroborates in Water
inferred← citeshttps://doi.org/10.1021/jo5009178openalex-snapshot
Palladium-Catalyzed Synthesis of Heterocycle-Containing Diarylmethanes through Suzuki–Miyaura Cross-Coupling
inferred← citeshttps://doi.org/10.1021/jo502062zopenalex-snapshot
C7-Derivatization of C3-Alkylindoles Including Tryptophans and Tryptamines
inferred← citeshttps://doi.org/10.1021/jo5025333openalex-snapshot
A Convergent Approach to the Total Synthesis of Telmisartan via a Suzuki Cross-Coupling Reaction between Two Functionalized Benzimidazoles
inferred← citeshttps://doi.org/10.1021/jo901441uopenalex-snapshot
Efficient Hydrolysis of Organotrifluoroborates via Silica Gel and Water
inferred← citeshttps://doi.org/10.1021/jo901641kopenalex-snapshot
From Imide to Lactam Metallo-pyridocarbazoles: Distinct Scaffolds for the Design of Selective Protein Kinase Inhibitors
inferred← citeshttps://doi.org/10.1021/jo902647hopenalex-snapshot
Palladium-Catalyzed Preparation of Weinreb Amides from Boronic Acids and N-Methyl-N-methoxycarbamoyl Chloride
inferred← citeshttps://doi.org/10.1021/ol100671vopenalex-snapshot
General Method for Synthesis of 2-Heterocyclic N-Methyliminodiacetic Acid Boronates
inferred← citeshttps://doi.org/10.1021/ol101592ropenalex-snapshot
Nickel-Catalyzed C−O Activation of Phenol Derivatives with Potassium Heteroaryltrifluoroborates
inferred← citeshttps://doi.org/10.1021/ol102039copenalex-snapshot
Synthesis of Amidomethyltrifluoroborates and Their Use in Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1021/ol102717xopenalex-snapshot
Nickel-Catalyzed Cross-Coupling of Potassium Aryl- and Heteroaryltrifluoroborates with Unactivated Alkyl Halides
inferred← citeshttps://doi.org/10.1021/ol300215popenalex-snapshot
Synthesis and Reactivity of Solid-Supported Organotrifluoroborates in Suzuki Cross-Coupling
inferred← citeshttps://doi.org/10.1021/ol301956popenalex-snapshot
Oxidative Condensations To Form Benzimidazole-Substituted Potassium Organotrifluoroborates
inferred← citeshttps://doi.org/10.1021/ol3022897openalex-snapshot
Preparation of Brominated 2-Alkoxythiophenes via Oxidation and Etherification of 2-Thienyltrifluoroborate Salts
inferred← citeshttps://doi.org/10.1021/ol302418bopenalex-snapshot
Synthesis of Ynone Trifluoroborates toward Functionalized Pyrazoles
inferred← citeshttps://doi.org/10.1021/ol4010189openalex-snapshot
Ether-Imidazolium Carbenes for Suzuki–Miyaura Cross-Coupling of Heteroaryl Chlorides with Aryl/Heteroarylboron Reagents
inferred← citeshttps://doi.org/10.1021/ol402268gopenalex-snapshot
Tetrabutylammonium 2-Pyridyltriolborate Salts for Suzuki–Miyaura Cross-Coupling Reactions with Aryl Chlorides
inferred← citeshttps://doi.org/10.1021/ol402798zopenalex-snapshot
Synthesis of Solid 2-Pyridylzinc Reagents and Their Application in Negishi Reactions
inferred← citeshttps://doi.org/10.1021/ol500057aopenalex-snapshot
Development of the Direct Suzuki–Miyaura Cross-Coupling of Primary B-Alkyl MIDA-boronates and Aryl Bromides
inferred← citeshttps://doi.org/10.1021/ol503479gopenalex-snapshot
Two-Step Cyanomethylation Protocol: Convenient Access to Functionalized Aryl- and Heteroarylacetonitriles
inferred← citeshttps://doi.org/10.1021/ol901395copenalex-snapshot
Condensation Reactions To Form Oxazoline-Substituted Potassium Organotrifluoroborates
inferred← citeshttps://doi.org/10.1021/ol902573xopenalex-snapshot
Ambient Temperature Nitrogen-Directed Difluoroalkynylborane Carboni−Lindsey Cycloaddition Reactions
inferred← citeshttps://doi.org/10.1021/om500520zopenalex-snapshot
Palladium-Catalyzed Suzuki–Miyaura Cross-Couplings with 2-Diethylphosphonato-Substituted Aryl- and Naphthylboronate Esters as the Nucleophilic Partner: A Complementary Approach to the Synthesis of Biaryl Monophosphonates
inferred← citeshttps://doi.org/10.1021/om900460uopenalex-snapshot
Synthesis, Structures, and Characterizations of [ArTi(O-i-Pr)3]2and Efficient Room-Temperature Aryl−Aryl Coupling of Aryl Bromides with [ArTi(O-i-Pr)3]2Catalyzed by the Economic Pd(OAc)2/PCy3System
inferred← citeshttps://doi.org/10.1038/s41929-021-00719-6openalex-snapshot
Lewis acid-mediated Suzuki–Miyaura cross-coupling reaction
inferred← citeshttps://doi.org/10.1039/c0gc00229aopenalex-snapshot
Carbonates: eco-friendly solvents for palladium-catalysed direct arylation of heteroaromatics
inferred← citeshttps://doi.org/10.1039/c1cc15990aopenalex-snapshot
Suzuki-Miyaura coupling of heteroaryl boronic acids and vinyl chlorides
inferred← citeshttps://doi.org/10.1039/c4ob00898gopenalex-snapshot
Convenient access to readily soluble symmetrical dialkyl-substituted α-oligofurans
inferred← citeshttps://doi.org/10.1039/c5ra05952fopenalex-snapshot
Pd and Pd–CuO nanoparticles in hollow silicalite-1 single crystals for enhancing selectivity and activity for the Suzuki–Miyaura reaction
inferred← citeshttps://doi.org/10.1039/c5ra10001aopenalex-snapshot
Palladium-catalyzed ligand-free and efficient Suzuki–Miyaura reaction of heteroaryl halides with MIDA boronates in water
inferred← citeshttps://doi.org/10.1039/c6ob00584eopenalex-snapshot
Palladium-catalyzed direct desulfitative C2 arylations of 3-halo-N-protected indoles using (hetero)arenesulfonyl chlorides
inferred← citeshttps://doi.org/10.1039/c6ob01126hopenalex-snapshot
Palladium-catalyzed β-(hetero)arylation of α,β-unsaturated valerolactams
inferred← citeshttps://doi.org/10.1039/c7ob02601copenalex-snapshot
Pd-Catalyzed one-pot sequential cross-coupling reactions of tetrabromothiophene
inferred← citeshttps://doi.org/10.1039/c7ra01087gopenalex-snapshot
Continuous flow synthesis of indoles by Pd-catalyzed deoxygenation of 2-nitrostilbenes with carbon monoxide
inferred← citeshttps://doi.org/10.1039/c7sc05420copenalex-snapshot
Rapid access to diverse, trifluoromethyl-substituted alkenes using complementary strategies
showing the first 200 of 235 · page through all 235
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.