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Glosář Rezonovat Nadace palladium carbene catalyst thiol Zámek Maryanne Jonesová potrubí

Recent Progress in the Use of Pd-Catalyzed C-C Cross-Coupling Reactions in the Synthesis of Pharmaceutical Compounds
Recent Progress in the Use of Pd-Catalyzed C-C Cross-Coupling Reactions in the Synthesis of Pharmaceutical Compounds

A novel tetrazole functionalized polymer-supported palladium nano-catalyst for the synthesis of various N-benzylated arylcyanamides - J. Alloys Compd. - X-MOL
A novel tetrazole functionalized polymer-supported palladium nano-catalyst for the synthesis of various N-benzylated arylcyanamides - J. Alloys Compd. - X-MOL

Cellulose-supported N-heterocyclic carbene-palladium catalyst: synthesis and its applications in the Suzuki cross-coupling reaction. | Semantic Scholar
Cellulose-supported N-heterocyclic carbene-palladium catalyst: synthesis and its applications in the Suzuki cross-coupling reaction. | Semantic Scholar

Palladium-catalyzed Suzuki-Miyaura coupling of thioureas or thioamides | Nature Communications
Palladium-catalyzed Suzuki-Miyaura coupling of thioureas or thioamides | Nature Communications

Preventing Pd–NHC bond cleavage and switching from nano-scale to molecular catalytic systems: amines and temperature as catalyst activators - Catalysis Science & Technology (RSC Publishing)
Preventing Pd–NHC bond cleavage and switching from nano-scale to molecular catalytic systems: amines and temperature as catalyst activators - Catalysis Science & Technology (RSC Publishing)

Molecules | Free Full-Text | Sulfur-Functionalized N-Heterocyclic Carbene Complexes of Pd(II): Syntheses, Structures and Catalytic Activities | HTML
Molecules | Free Full-Text | Sulfur-Functionalized N-Heterocyclic Carbene Complexes of Pd(II): Syntheses, Structures and Catalytic Activities | HTML

Magnetically recoverable nanostructured Pd complex of dendrimeric type ligand on the MCM-41: Preparation, characterization and catalytic activity in the Heck reaction in: Main Group Metal Chemistry Volume 43 Issue 1 (2020)
Magnetically recoverable nanostructured Pd complex of dendrimeric type ligand on the MCM-41: Preparation, characterization and catalytic activity in the Heck reaction in: Main Group Metal Chemistry Volume 43 Issue 1 (2020)

Carbon-Carbon Cross Coupling Reactions in Ionic Liquids Catalysed by Palladium Metal Nanoparticles – topic of research paper in Chemical sciences. Download scholarly article PDF and read for free on CyberLeninka open science
Carbon-Carbon Cross Coupling Reactions in Ionic Liquids Catalysed by Palladium Metal Nanoparticles – topic of research paper in Chemical sciences. Download scholarly article PDF and read for free on CyberLeninka open science

A synthesis of biaryl ketones via the C–S bond cleavage of thiol ester by a Cu/Ag salt - Tetrahedron Lett. - X-MOL
A synthesis of biaryl ketones via the C–S bond cleavage of thiol ester by a Cu/Ag salt - Tetrahedron Lett. - X-MOL

Thiol Treatment Creates Selective Palladium Catalysts for Semihydrogenation of Internal Alkynes - ScienceDirect
Thiol Treatment Creates Selective Palladium Catalysts for Semihydrogenation of Internal Alkynes - ScienceDirect

PDF) Polymer-Supported Palladium(II) Carbene Complexes: Catalytic Activity, Recyclability, and Selectivity in C-H Acetoxylation of Arenes
PDF) Polymer-Supported Palladium(II) Carbene Complexes: Catalytic Activity, Recyclability, and Selectivity in C-H Acetoxylation of Arenes

Palladium N-heterocyclic carbene catalyzed regioselective thiolation of 1-aryl-3-methyl-1H-pyrazol-5(4H)-ones using aryl thiols - ScienceDirect
Palladium N-heterocyclic carbene catalyzed regioselective thiolation of 1-aryl-3-methyl-1H-pyrazol-5(4H)-ones using aryl thiols - ScienceDirect

Various [NHC-Pd-PEPPSI] (left) and long alkyl chain-labeled... | Download Scientific Diagram
Various [NHC-Pd-PEPPSI] (left) and long alkyl chain-labeled... | Download Scientific Diagram

Synthetic Routes to Late Transition Metal–NHC Complexes: Trends in Chemistry
Synthetic Routes to Late Transition Metal–NHC Complexes: Trends in Chemistry

Aryl sulfide or diaryl sulfide synthesis by S-arylation or S-alkylation
Aryl sulfide or diaryl sulfide synthesis by S-arylation or S-alkylation

Palladium-catalyzed carbon-sulfur or carbon-phosphorus bond metathesis by reversible arylation | Science
Palladium-catalyzed carbon-sulfur or carbon-phosphorus bond metathesis by reversible arylation | Science

Tuning the Catalytic Activity and Selectivity of Pd Nanoparticles Using Ligand-Modified Supports and Surfaces
Tuning the Catalytic Activity and Selectivity of Pd Nanoparticles Using Ligand-Modified Supports and Surfaces

Palladium‐Catalyzed C–S Bond Formation: Rate and Mechanism of the Coupling of Aryl or Vinyl Halides with a Thiol Derived from a Cysteine - Moreau - 2005 - European Journal of Organic Chemistry -
Palladium‐Catalyzed C–S Bond Formation: Rate and Mechanism of the Coupling of Aryl or Vinyl Halides with a Thiol Derived from a Cysteine - Moreau - 2005 - European Journal of Organic Chemistry -

Thiol Treatment Creates Selective Palladium Catalysts for Semihydrogenation of Internal Alkynes - ScienceDirect
Thiol Treatment Creates Selective Palladium Catalysts for Semihydrogenation of Internal Alkynes - ScienceDirect

Alkyne Hydrothiolation Catalyzed by a Dichlorobis(aminophosphine) Complex of Palladium: Selective Formation of cis‐Configured Vinyl Thioethers - Gerber - 2012 - Chemistry – A European Journal - Wiley Online Library
Alkyne Hydrothiolation Catalyzed by a Dichlorobis(aminophosphine) Complex of Palladium: Selective Formation of cis‐Configured Vinyl Thioethers - Gerber - 2012 - Chemistry – A European Journal - Wiley Online Library

Palladium‐Catalyzed C–S Bond Formation: Rate and Mechanism of the Coupling of Aryl or Vinyl Halides with a Thiol Derived from a Cysteine - Moreau - 2005 - European Journal of Organic Chemistry -
Palladium‐Catalyzed C–S Bond Formation: Rate and Mechanism of the Coupling of Aryl or Vinyl Halides with a Thiol Derived from a Cysteine - Moreau - 2005 - European Journal of Organic Chemistry -

Ten-fold boost of catalytic performance in thiol–yne click reaction enabled by a palladium diketonate complex with a hexafluoroacetylacetonate ligand - Catalysis Science & Technology (RSC Publishing)
Ten-fold boost of catalytic performance in thiol–yne click reaction enabled by a palladium diketonate complex with a hexafluoroacetylacetonate ligand - Catalysis Science & Technology (RSC Publishing)

Ten-fold boost of catalytic performance in thiol–yne click reaction enabled by a palladium diketonate complex with a hexafluoroacetylacetonate ligand - Catalysis Science & Technology (RSC Publishing)
Ten-fold boost of catalytic performance in thiol–yne click reaction enabled by a palladium diketonate complex with a hexafluoroacetylacetonate ligand - Catalysis Science & Technology (RSC Publishing)

Palladium/Nucleophilic Carbene Catalysts for Cross-Coupling Reactions | Johnson Matthey Technology Review
Palladium/Nucleophilic Carbene Catalysts for Cross-Coupling Reactions | Johnson Matthey Technology Review

Catalysts | Free Full-Text | The Combination of Lewis Acid with N-Heterocyclic Carbene (NHC) Catalysis | HTML
Catalysts | Free Full-Text | The Combination of Lewis Acid with N-Heterocyclic Carbene (NHC) Catalysis | HTML

Application of Thiol-Modified Dual-Pore Silica Beads as a Practical Scavenger of Leached Palladium Catalyst in C–C Coupling Reactions - Org. Process Res. Dev. - X-MOL
Application of Thiol-Modified Dual-Pore Silica Beads as a Practical Scavenger of Leached Palladium Catalyst in C–C Coupling Reactions - Org. Process Res. Dev. - X-MOL

Sonogashira coupling - Wikipedia
Sonogashira coupling - Wikipedia

Aryl sulfide or diaryl sulfide synthesis by S-arylation or S-alkylation
Aryl sulfide or diaryl sulfide synthesis by S-arylation or S-alkylation