![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](https://ars.els-cdn.com/content/image/1-s2.0-S0040402016300126-fx1.jpg)
Palladium N-heterocyclic carbene catalyzed regioselective thiolation of 1-aryl-3-methyl-1H-pyrazol-5(4H)-ones using aryl thiols - ScienceDirect
![PDF) Ultra‐small sugar‐substituted N‐heterocyclic carbene‐protected palladium nanoparticles and catalytic activity PDF) Ultra‐small sugar‐substituted N‐heterocyclic carbene‐protected palladium nanoparticles and catalytic activity](https://www.researchgate.net/profile/Zhong-Gao_Zhou/publication/332417523/figure/fig1/AS:860843151466496@1582252409180/Synthesis-of-sugar-substituted-NHC-precursors_Q320.jpg)
PDF) Ultra‐small sugar‐substituted N‐heterocyclic carbene‐protected palladium nanoparticles and catalytic activity
![EP1022282A2 - Homo- and hetero metal alkylidene complexes of ruthenium with N-heterocyclic carbene ligands, and their use as highly active and selective catalysts for olefin metathesis - Google Patents EP1022282A2 - Homo- and hetero metal alkylidene complexes of ruthenium with N-heterocyclic carbene ligands, and their use as highly active and selective catalysts for olefin metathesis - Google Patents](https://patentimages.storage.googleapis.com/94/25/19/a0eac9a2808212/00040002.png)
EP1022282A2 - Homo- and hetero metal alkylidene complexes of ruthenium with N-heterocyclic carbene ligands, and their use as highly active and selective catalysts for olefin metathesis - Google Patents
![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](https://ars.els-cdn.com/content/image/1-s2.0-S0040402016300126-sc1.jpg)
Palladium N-heterocyclic carbene catalyzed regioselective thiolation of 1-aryl-3-methyl-1H-pyrazol-5(4H)-ones using aryl thiols - ScienceDirect
![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 -](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/83e56d54-efc6-4284-9caa-e26459bc3495/mscheme15.jpg)
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 -
![Recent advances in the catalytic applications of GO/rGO for green organic synthesis in: Green Processing and Synthesis Volume 9 Issue 1 (2020) Recent advances in the catalytic applications of GO/rGO for green organic synthesis in: Green Processing and Synthesis Volume 9 Issue 1 (2020)](https://www.degruyter.com/abstract/journals/gps/9/1/graphic/j_gps-2020-0055_fig_009.jpg)
Recent advances in the catalytic applications of GO/rGO for green organic synthesis in: Green Processing and Synthesis Volume 9 Issue 1 (2020)
![Recent advances in the Suzuki–Miyaura cross-coupling reaction using efficient catalysts in eco-friendly media - Green Chemistry (RSC Publishing) DOI:10.1039/C8GC02860E Recent advances in the Suzuki–Miyaura cross-coupling reaction using efficient catalysts in eco-friendly media - Green Chemistry (RSC Publishing) DOI:10.1039/C8GC02860E](https://pubs.rsc.org/image/article/2019/GC/c8gc02860e/c8gc02860e-s13_hi-res.gif)
Recent advances in the Suzuki–Miyaura cross-coupling reaction using efficient catalysts in eco-friendly media - Green Chemistry (RSC Publishing) DOI:10.1039/C8GC02860E
![Robust gold nanorods stabilized by bidentate N-heterocyclic-carbene–thiolate ligands | Nature Chemistry Robust gold nanorods stabilized by bidentate N-heterocyclic-carbene–thiolate ligands | Nature Chemistry](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41557-018-0159-8/MediaObjects/41557_2018_159_Figa_HTML.png)
Robust gold nanorods stabilized by bidentate N-heterocyclic-carbene–thiolate ligands | Nature Chemistry
![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](https://ars.els-cdn.com/content/image/1-s2.0-S0040402016300126-sc2.jpg)
Palladium N-heterocyclic carbene catalyzed regioselective thiolation of 1-aryl-3-methyl-1H-pyrazol-5(4H)-ones using aryl thiols - ScienceDirect
![Molecules | Free Full-Text | Macrocyclic Drugs and Synthetic Methodologies toward Macrocycles | HTML Molecules | Free Full-Text | Macrocyclic Drugs and Synthetic Methodologies toward Macrocycles | HTML](https://www.mdpi.com/molecules/molecules-18-06230/article_deploy/html/images/molecules-18-06230-g016.png)
Molecules | Free Full-Text | Macrocyclic Drugs and Synthetic Methodologies toward Macrocycles | HTML
![Molecules | Free Full-Text | Recyclable Nanostructured Catalytic Systems in Modern Environmentally Friendly Organic Synthesis | HTML Molecules | Free Full-Text | Recyclable Nanostructured Catalytic Systems in Modern Environmentally Friendly Organic Synthesis | HTML](https://www.mdpi.com/molecules/molecules-15-04792/article_deploy/html/images/molecules-15-04792-g011.png)
Molecules | Free Full-Text | Recyclable Nanostructured Catalytic Systems in Modern Environmentally Friendly Organic Synthesis | HTML
![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](https://ars.els-cdn.com/content/image/1-s2.0-S0040402016300126-sc3.jpg)
Palladium N-heterocyclic carbene catalyzed regioselective thiolation of 1-aryl-3-methyl-1H-pyrazol-5(4H)-ones using aryl thiols - ScienceDirect
![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 -](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/16c94bd0-d6e4-44c5-94b2-5ab3a6ff5a23/mscheme1.jpg)
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 - 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 -](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/8f1cb822-3ec6-4ca2-b770-08b248d2cc9d/mscheme12.jpg)
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 -
![Pd nanoparticles stabilized on the Schiff base-modified boehmite: Catalytic role in Suzuki coupling reaction and reduction of nitroarenes - ScienceDirect Pd nanoparticles stabilized on the Schiff base-modified boehmite: Catalytic role in Suzuki coupling reaction and reduction of nitroarenes - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0022328X19303596-sc1.jpg)
Pd nanoparticles stabilized on the Schiff base-modified boehmite: Catalytic role in Suzuki coupling reaction and reduction of nitroarenes - ScienceDirect
![N-heterocyclic carbene metal complexes as bio-organometallic antimicrobial and anticancer drugs | Future Medicinal Chemistry N-heterocyclic carbene metal complexes as bio-organometallic antimicrobial and anticancer drugs | Future Medicinal Chemistry](https://www.future-science.com/cms/10.4155/fmc.15.61/asset/images/medium/figure12.gif)
N-heterocyclic carbene metal complexes as bio-organometallic antimicrobial and anticancer drugs | Future Medicinal Chemistry
![PDF) ChemInform Abstract: Sulfur-Functionalized N-Heterocyclic Carbene Complexes of Pd(II): Syntheses, Structures and Catalytic Activities PDF) ChemInform Abstract: Sulfur-Functionalized N-Heterocyclic Carbene Complexes of Pd(II): Syntheses, Structures and Catalytic Activities](https://i1.rgstatic.net/publication/221881232_ChemInform_Abstract_Sulfur-Functionalized_N-Heterocyclic_Carbene_Complexes_of_PdII_Syntheses_Structures_and_Catalytic_Activities/links/02e7e515d4e5beb229000000/largepreview.png)
PDF) ChemInform Abstract: Sulfur-Functionalized N-Heterocyclic Carbene Complexes of Pd(II): Syntheses, Structures and Catalytic Activities
![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 -](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/1708433f-5394-40ed-b3d0-2d832ebc34a9/mscheme13.jpg)
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 - 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 -](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/ada1ba18-601c-4b4f-9382-61671c93f728/mscheme9.gif)
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 - 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 -](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/cd9b9a60-8a98-4187-bfb7-67e801840c2d/mscheme3.jpg)
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 -
![Encapsulating palladium nanoparticles inside ethylenediamine functionalized and crosslinked chlorinated poly(vinyl chloride) nanofibers as an efficient and stable heterogeneous catalyst for coupling reactions - J. Phys. Chem. Solids - X-MOL Encapsulating palladium nanoparticles inside ethylenediamine functionalized and crosslinked chlorinated poly(vinyl chloride) nanofibers as an efficient and stable heterogeneous catalyst for coupling reactions - J. Phys. Chem. Solids - X-MOL](https://xpic.x-mol.com/20200731%2F10.1016_j.jpcs.2020.109674.jpg)
Encapsulating palladium nanoparticles inside ethylenediamine functionalized and crosslinked chlorinated poly(vinyl chloride) nanofibers as an efficient and stable heterogeneous catalyst for coupling reactions - J. Phys. Chem. Solids - X-MOL
![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 -](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/8f5de3c5-f70d-485a-8f63-d22ac4b2ebcd/mscheme8.jpg)