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Excellent Suzuki–Miyauracatalytic activity of a new Pd(II) complex with sulfonamide–Schiff base ligand

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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A Highly Active Catalyst for the Room-Temperature Amination and Suzuki Coupling of Aryl Chlorides

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Palladium-Catalyzed Coupling Reactions of Aryl Chlorides

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An Efficient Palladium N‐Heterocyclic Carbene Catalyst Allowing the Suzuki–Miyaura Cross‐Coupling of Aryl Chlorides and Arylboronic Acids at Room Temperature in Aqueous Solution

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Au–Pd Core–Shell Nanoparticles Catalyze Suzuki–Miyaura Reactions in Water through Pd Leaching

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Palladium‐Catalyzed Cross‐Coupling: A Historical Contextual Perspective to the 2010 Nobel Prize

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Synthesis, characterization and catalytic properties of novel palladium(II) complexes containing aromatic sulfonamides: effective catalysts for the oxidation of benzyl alcohol

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Pd(II) complexes of Schiff bases and their application as catalysts in Mizoroki–Heck and Suzuki–Miyaura cross‐coupling reactions

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Mechanistic Origin of Antagonist Effects of Usual Anionic Bases (OH−, CO32−) as Modulated by their Countercations (Na+, Cs+, K+) in Palladium‐Catalyzed Suzuki–Miyaura Reactions

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Synthesis of Chlorinated Biphenyls by Suzuki Cross‐Coupling Using Diamine or Diimine‐Palladium Complexes

inferredcites →https://doi.org/10.1007/s11243-004-7625-4openalex-snapshot

Palladium(II) Schiff base complexes derived from sulfanilamides and aminobenzothiazoles

inferredcites →https://doi.org/10.1016/0040-6031(91)80021-aopenalex-snapshot

Thermal behaviour and electrical properties of some biologically active sulphonamide Schiff bases

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N,N,N′,N′-tetra(diphenylphosphinomethyl)pyridine-2,6-diamine/palladium catalyzed Suzuki–Miyaura coupling of aryl and heteroaryl halides

inferredcites →https://doi.org/10.1016/j.ccr.2007.09.005openalex-snapshot

Catalytic activities of Schiff base transition metal complexes

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Schiff base-derived homogeneous and heterogeneous palladium catalysts for the Suzuki–Miyaura reaction

inferredcites →https://doi.org/10.1016/j.ejmech.2009.10.044openalex-snapshot

Synthesis, antitumor activity and molecular docking study of novel Sulfonamide-Schiff's bases, thiazolidinones, benzothiazinones and their C-nucleoside derivatives

inferredcites →https://doi.org/10.1016/j.ica.2011.07.051openalex-snapshot

Palladium salicylaldimine complexes derived from 2,3-dihydroxybenzaldehyde

inferredcites →https://doi.org/10.1016/j.inoche.2009.10.023openalex-snapshot

Amino-salicylaldimine–palladium(II) complexes: New and efficient catalysts for Suzuki and Heck reactions

inferredcites →https://doi.org/10.1016/j.inoche.2012.05.006openalex-snapshot

A new two dimensional copper (II) coordination complex with sulphonamide: Synthesis, crystal structure and DNA binding study

inferredcites →https://doi.org/10.1016/j.jorganchem.2008.11.021openalex-snapshot

Mono- and dinuclear Pd(II) complexes of different salicylaldimine ligands as catalysts of transfer hydrogenation of nitrobenzene with cyclohexene and Suzuki–Miyaura coupling reactions

inferredcites →https://doi.org/10.1016/j.jorganchem.2014.08.002openalex-snapshot

Synthesis of some ruthenium(II)–Schiff base complexes bearing sulfonamide fragment: New catalysts for transfer hydrogenation of ketones

inferredcites →https://doi.org/10.1016/j.jorganchem.2014.10.047openalex-snapshot

Synthesis, characterization and the Suzuki–Miyaura coupling reactions of N-heterocyclic carbene–Pd(II)–pyridine (PEPPSI) complexes

inferredcites →https://doi.org/10.1016/j.molstruc.2015.02.042openalex-snapshot

Theoretical and experimental investigation of 4-[(2-hydroxy-3-methylbenzylidene)amino]benzenesulfonamide: Structural and spectroscopic properties, NBO, NLO and NPA analysis

inferredcites →https://doi.org/10.1016/j.poly.2014.09.042openalex-snapshot

Palladium(II) complexes bearing bidentate pyridyl-sulfonamide ligands: Synthesis and catalytic applications

inferredcites →https://doi.org/10.1016/j.saa.2006.04.033openalex-snapshot

Metal complexes of Schiff base derived from sulphametrole and o-vanilin

inferredcites →https://doi.org/10.1016/j.tet.2005.08.005openalex-snapshot

Palladium catalyzed Suzuki cross-coupling reactions using N,O-bidentate ligands

inferredcites →https://doi.org/10.1016/j.tet.2013.03.030openalex-snapshot

3-Indolylphosphines as ligand for palladium in Suzuki–Miyaura coupling reaction of chloroarenes: substituent effects

inferredcites →https://doi.org/10.1016/j.tet.2013.09.057openalex-snapshot

Increasing appendage diversity on 3,4-dihydro-3-oxo-2H-1,4-benzoxazines via Aphos–Pd(OAc)2-catalyzed Suzuki–Miyaura cross-coupling of aryl chlorides

inferredcites →https://doi.org/10.1016/j.tetlet.2008.03.109openalex-snapshot

Phosphine-free Pd–salen complexes as efficient and inexpensive catalysts for Heck and Suzuki reactions under aerobic conditions

inferredcites →https://doi.org/10.1016/j.tetlet.2008.08.056openalex-snapshot

Benzaldimines as ligands for palladium in Suzuki–Miyaura reactions

inferredcites →https://doi.org/10.1016/j.tetlet.2012.02.102openalex-snapshot

Highly effective activation of aryl chlorides for Suzuki coupling in aqueous media using a ferrocene-based Pd(II)–diimine catalyst

inferredcites →https://doi.org/10.1016/j.tetlet.2012.05.017openalex-snapshot

P,N-Type benzimidazolyl phosphine ligands for the palladium-catalyzed Suzuki coupling of potassium aryltrifluoroborates and aryl chlorides

inferredcites →https://doi.org/10.1016/j.tetlet.2012.08.026openalex-snapshot

Palladium(II) complex with a potential N4-type Schiff-base ligand as highly efficient catalyst for Suzuki–Miyaura reactions in aqueous media

inferredcites →https://doi.org/10.1016/j.tetlet.2013.03.115openalex-snapshot

A highly efficient Schiff-base derived palladium catalyst for the Suzuki–Miyaura reactions of aryl chlorides

inferredcites →https://doi.org/10.1016/j.tetlet.2014.01.041openalex-snapshot

A simple and efficient tetradentate Schiff base derived palladium complex for Suzuki–Miyaura reaction in water

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Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions Employing Dialkylbiaryl Phosphine Ligands

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The Development of Versatile Methods for Palladium-Catalyzed Coupling Reactions of Aryl Electrophiles through the Use of P(t-Bu)3 and PCy3 as Ligands

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Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds

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Versatile Catalysts for the Suzuki Cross-Coupling of Arylboronic Acids with Aryl and Vinyl Halides and Triflates under Mild Conditions

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A General Method for the Suzuki−Miyaura Cross-Coupling of Sterically Hindered Aryl Chlorides: Synthesis of Di- and Tri-ortho-substituted Biaryls in 2-Propanol at Room Temperature

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Modified (NHC)Pd(allyl)Cl (NHC = N-Heterocyclic Carbene) Complexes for Room-Temperature Suzuki−Miyaura and Buchwald−Hartwig Reactions

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A Highly Active Catalyst for Palladium-Catalyzed Cross-Coupling Reactions: Room-Temperature Suzuki Couplings and Amination of Unactivated Aryl Chlorides

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Phosphine-Free Hydrazone−Pd Complex as the Catalyst Precursor for a Suzuki−Miyaura Reaction under Mild Aerobic Conditions

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A Novel, Air-Stable Phosphine Ligand for the Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reaction of Chloro Arenes

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Carbon–Boron Bond Cross-Coupling Reaction Catalyzed by −PPh2 Containing Palladium–Indolylphosphine Complexes

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Palladium−Imidazol-2-ylidene Complexes as Catalysts for Facile and Efficient Suzuki Cross-Coupling Reactions of Aryl Chlorides with Arylboronic Acids

inferredcites →https://doi.org/10.1021/ol070898yopenalex-snapshot

Easily Accessible and Highly Tunable Indolyl Phosphine Ligands for Suzuki−Miyaura Coupling of Aryl Chlorides

inferredcites →https://doi.org/10.1021/ol102677ropenalex-snapshot

An Extremely Active and General Catalyst for Suzuki Coupling Reaction of Unreactive Aryl Chlorides

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Suzuki Coupling Reaction of Aryl Halides Catalyzed by an N-Heterocyclic Carbene−PdCl2 Species Based on a Porphyrin at Room Temperature

inferredcites →https://doi.org/10.1039/b006791lopenalex-snapshot

Molecularly defined palladium(0) monophosphine complexes as catalysts for efficient cross-coupling of aryl chlorides and phenylboronic acid1

inferredcites →https://doi.org/10.1039/b307853copenalex-snapshot

Metal–Salen Schiff base complexes in catalysis: practical aspects

inferredcites →https://doi.org/10.1039/b407243jopenalex-snapshot

A simple and highly efficient P,O-type ligand for Suzuki–Miyaura cross-coupling of aryl halides

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Green chemistry tools to influence a medicinal chemistry and research chemistry based organisation

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In situ formation of N,O-bidentate ligand via the hydrogen bond for highly efficient Suzuki reaction of aryl chlorides

inferredcites →https://doi.org/10.1039/c0cc05487aopenalex-snapshot

Epoxidation of alkenes and oxidation of alcohols with hydrogen peroxide catalyzed by a manganese(v) nitrido complex

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Highly efficient carbazolyl-derived phosphine ligands: application to sterically hindered biaryl couplings

inferredcites →https://doi.org/10.1039/c1cs15079kopenalex-snapshot

Nanocatalysts for Suzuki cross-coupling reactions

inferredcites →https://doi.org/10.1039/c1dt11695aopenalex-snapshot

Palladium( ii )-selenated Schiff base complex catalyzed Suzuki–Miyaura coupling: Dependence of efficiency on alkyl chain length of ligand

inferredcites →https://doi.org/10.1039/c3cs60197hopenalex-snapshot

Selection of boron reagents for Suzuki–Miyaura coupling

inferredcites →https://doi.org/10.1039/c4ob00846dopenalex-snapshot

A general catalyst for Suzuki–Miyaura and Sonogashira reactions of aryl and heteroaryl chlorides in water

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Aromatic Schiff bases and 2,3-disubstituted-1,3-thiazolidin-4-one derivatives as antiinflammatory agents

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Synthesis of novel allyl palladium complexes bearing purine based NHC and a water soluble phosphine and their catalytic activity in the Suzuki‐Miyaura coupling in water

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ChemInform Abstract: Excellent Suzuki—Miyaura Catalytic Activity of a New Pd(II) Complex with Sulfonamide—Schiff Base Ligand.

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Schiff Base/CuI as a Novel Efficient Catalyst System for Cu–Catalyzed Heck Reaction in Water

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Binuclear Pd(II) complexes with multidentate Schiff base ligands: synthesis, catalysis, and antibacterial properties

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Effect of ligand tautomerism on Suzuki reactions

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2017.05.049openalex-snapshot

Synthesis and characterization of a new Pd(II)-Schiff base complex [Pd(APD)2]: An efficient and recyclable catalyst for Heck-Mizoroki and Suzuki-Miyaura reactions

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Synthesis of brominated bisamides and their application to the suzuki coupling

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Suzuki−Miyaura coupling and O−arylation reactions catalysed by palladium(II) complexes of bulky ligands bearing naphthalene core, Schiff base functionality and biarylphosphine moiety

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Palladium-Catalyzed Suzuki−Miyaura cross-coupling reactions employing hydrazone-thioether ligands in aqueous media under IR-irradiation

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Nickel (II) complex [NiCl2(DMF)2L2] bearing diaminobenzene and sulfonamide: Crystal structure and catalytic application in the reduction of nitrobenzenes

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O-arylation reaction over lanthanide metal–organic framework: Synthesis, structure and catalytic reaction

inferred← citeshttps://doi.org/10.1039/c9nj02977jopenalex-snapshot

Thiazole-based non-symmetric NNC–palladium pincer complexes as catalytic precursors for the Suzuki–Miyaura C–C coupling

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Synthesis, Spectral and Catalytic Properties of Palladium(II) Complexes Containing Hydrazone Schiff Base Ligands

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