![Synthesis of bridged palladium-PEPPSI complexes and catalytic studies in C–C cross-coupling reactions - ScienceDirect Synthesis of bridged palladium-PEPPSI complexes and catalytic studies in C–C cross-coupling reactions - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0020169319306541-ga1.jpg)
Synthesis of bridged palladium-PEPPSI complexes and catalytic studies in C–C cross-coupling reactions - ScienceDirect
![A mesoionic bis(Py- tz NHC) palladium( ii ) complex catalyses “green” Sonogashira reaction through an unprecedented mechanism - Chemical Communications (RSC Publishing) DOI:10.1039/C5CC08717A A mesoionic bis(Py- tz NHC) palladium( ii ) complex catalyses “green” Sonogashira reaction through an unprecedented mechanism - Chemical Communications (RSC Publishing) DOI:10.1039/C5CC08717A](https://pubs.rsc.org/image/article/2016/CC/c5cc08717a/c5cc08717a-f1_hi-res.gif)
A mesoionic bis(Py- tz NHC) palladium( ii ) complex catalyses “green” Sonogashira reaction through an unprecedented mechanism - Chemical Communications (RSC Publishing) DOI:10.1039/C5CC08717A
![Cyclometalated Palladium NHC Complexes Bearing PEG Chains for Suzuki–Miyaura Cross-Coupling in Water - Organometallics - X-MOL Cyclometalated Palladium NHC Complexes Bearing PEG Chains for Suzuki–Miyaura Cross-Coupling in Water - Organometallics - X-MOL](https://xpic.x-mol.com/20181107%2F10.1021_acs.organomet.8b00607.jpg)
Cyclometalated Palladium NHC Complexes Bearing PEG Chains for Suzuki–Miyaura Cross-Coupling in Water - Organometallics - X-MOL
![Adamantanyl-substituted PEPPSI-type palladium(II) N-heterocyclic carbene complexes: synthesis and catalytic application for CH activation of substituted thiophenes | SpringerLink Adamantanyl-substituted PEPPSI-type palladium(II) N-heterocyclic carbene complexes: synthesis and catalytic application for CH activation of substituted thiophenes | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10593-019-02445-1/MediaObjects/10593_2019_2445_Figa_HTML.jpg)
Adamantanyl-substituted PEPPSI-type palladium(II) N-heterocyclic carbene complexes: synthesis and catalytic application for CH activation of substituted thiophenes | SpringerLink
![A new PEPPSI type N-heterocyclic carbene palladium(II) complex and its efficiency as a catalyst for Mizoroki-Heck cross-coupling reactions in water | SpringerLink A new PEPPSI type N-heterocyclic carbene palladium(II) complex and its efficiency as a catalyst for Mizoroki-Heck cross-coupling reactions in water | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs12039-020-1754-y/MediaObjects/12039_2020_1754_Sch2_HTML.png)
A new PEPPSI type N-heterocyclic carbene palladium(II) complex and its efficiency as a catalyst for Mizoroki-Heck cross-coupling reactions in water | SpringerLink
![Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML](https://www.mdpi.com/catalysts/catalysts-10-00004/article_deploy/html/images/catalysts-10-00004-sch022.png)
Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML
![Calixarene-supported Pd–NHC complexes as efficient catalysts for scalable Suzuki–Miyaura cross-couplings - React. Chem. Eng. - X-MOL Calixarene-supported Pd–NHC complexes as efficient catalysts for scalable Suzuki–Miyaura cross-couplings - React. Chem. Eng. - X-MOL](https://xpic.x-mol.com/20200729%2F10.1039_D0RE00118J.jpg)
Calixarene-supported Pd–NHC complexes as efficient catalysts for scalable Suzuki–Miyaura cross-couplings - React. Chem. Eng. - X-MOL
Continuous flow Negishi cross-couplings employing silica-supported Pd-PEPPSI–IPr precatalyst - Catalysis Science & Technology (RSC Publishing)
![Amino acid-derived N-heterocyclic carbene palladium complexes for aqueous phase Suzuki–Miyaura couplings - New Journal of Chemistry (RSC Publishing) Amino acid-derived N-heterocyclic carbene palladium complexes for aqueous phase Suzuki–Miyaura couplings - New Journal of Chemistry (RSC Publishing)](https://pubs.rsc.org/image/article/2016/nj/c5nj03337c/c5nj03337c-s2_hi-res.gif)
Amino acid-derived N-heterocyclic carbene palladium complexes for aqueous phase Suzuki–Miyaura couplings - New Journal of Chemistry (RSC Publishing)
![Synthesis, characterization and catalytic activity of PEPPSI-type palladium–NHC complexes - ScienceDirect Synthesis, characterization and catalytic activity of PEPPSI-type palladium–NHC complexes - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0020169320312433-gr1.jpg)
Synthesis, characterization and catalytic activity of PEPPSI-type palladium–NHC complexes - ScienceDirect
![Catalysts | Free Full-Text | Palladium PEPPSI-IPr Complex Supported on a Calix[8]arene: A New Catalyst for Efficient Suzuki–Miyaura Coupling of Aryl Chlorides | HTML Catalysts | Free Full-Text | Palladium PEPPSI-IPr Complex Supported on a Calix[8]arene: A New Catalyst for Efficient Suzuki–Miyaura Coupling of Aryl Chlorides | HTML](https://www.mdpi.com/catalysts/catalysts-10-01081/article_deploy/html/images/catalysts-10-01081-i001.png)
Catalysts | Free Full-Text | Palladium PEPPSI-IPr Complex Supported on a Calix[8]arene: A New Catalyst for Efficient Suzuki–Miyaura Coupling of Aryl Chlorides | HTML
![Pd‐PEPPSI Complexes and the Negishi Reaction - Valente - 2010 - European Journal of Organic Chemistry - Wiley Online Library Pd‐PEPPSI Complexes and the Negishi Reaction - Valente - 2010 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/d0d444ce-b54a-4eec-9cf2-58aa9ca99e63/mfig000.jpg)
Pd‐PEPPSI Complexes and the Negishi Reaction - Valente - 2010 - European Journal of Organic Chemistry - Wiley Online Library
![A new PEPPSI type N-heterocyclic carbene palladium(II) complex and its efficiency as a catalyst for Mizoroki-Heck cross-coupling reactions in water | SpringerLink A new PEPPSI type N-heterocyclic carbene palladium(II) complex and its efficiency as a catalyst for Mizoroki-Heck cross-coupling reactions in water | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs12039-020-1754-y/MediaObjects/12039_2020_1754_Sch1_HTML.png)
A new PEPPSI type N-heterocyclic carbene palladium(II) complex and its efficiency as a catalyst for Mizoroki-Heck cross-coupling reactions in water | SpringerLink
![Investigation of activity, stability, and degradation mechanism of surface-supported Pd-PEPPSI complexes for Suzuki-Miyaura coupling - ScienceDirect Investigation of activity, stability, and degradation mechanism of surface-supported Pd-PEPPSI complexes for Suzuki-Miyaura coupling - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1381116916305477-fx1.jpg)
Investigation of activity, stability, and degradation mechanism of surface-supported Pd-PEPPSI complexes for Suzuki-Miyaura coupling - ScienceDirect
![Catalysts | Free Full-Text | Palladium PEPPSI-IPr Complex Supported on a Calix[8]arene: A New Catalyst for Efficient Suzuki–Miyaura Coupling of Aryl Chlorides | HTML Catalysts | Free Full-Text | Palladium PEPPSI-IPr Complex Supported on a Calix[8]arene: A New Catalyst for Efficient Suzuki–Miyaura Coupling of Aryl Chlorides | HTML](https://www.mdpi.com/catalysts/catalysts-10-01081/article_deploy/html/images/catalysts-10-01081-i002.png)
Catalysts | Free Full-Text | Palladium PEPPSI-IPr Complex Supported on a Calix[8]arene: A New Catalyst for Efficient Suzuki–Miyaura Coupling of Aryl Chlorides | HTML
![Cycloheptyl substituted N-heterocyclic carbene PEPPSI-type palladium complexes with different N-coordinated ligands: Involvement in Suzuki-Miyaura reaction - ScienceDirect Cycloheptyl substituted N-heterocyclic carbene PEPPSI-type palladium complexes with different N-coordinated ligands: Involvement in Suzuki-Miyaura reaction - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0022328X19303493-fx1.jpg)
Cycloheptyl substituted N-heterocyclic carbene PEPPSI-type palladium complexes with different N-coordinated ligands: Involvement in Suzuki-Miyaura reaction - ScienceDirect
![Aqueous-Phase Chemistry of η3-Allylpalladium(II) Complexes with Sulfonated N-Heterocyclic Carbene Ligands: Solvent Effects in the Protolysis of Pd–C Bonds and Suzuki–Miyaura Reactions - Organometallics - X-MOL Aqueous-Phase Chemistry of η3-Allylpalladium(II) Complexes with Sulfonated N-Heterocyclic Carbene Ligands: Solvent Effects in the Protolysis of Pd–C Bonds and Suzuki–Miyaura Reactions - Organometallics - X-MOL](https://xpic.x-mol.com/20171021%2F10.1021_acs.organomet.7b00635.jpg)
Aqueous-Phase Chemistry of η3-Allylpalladium(II) Complexes with Sulfonated N-Heterocyclic Carbene Ligands: Solvent Effects in the Protolysis of Pd–C Bonds and Suzuki–Miyaura Reactions - Organometallics - X-MOL
![Facile-prepared sulfonated water-soluble PEPPSI-Pd-NHC catalysts for aerobic aqueous Suzuki–Miyaura cross-coupling reactions - Green Chemistry (RSC Publishing) DOI:10.1039/C4GC00986J Facile-prepared sulfonated water-soluble PEPPSI-Pd-NHC catalysts for aerobic aqueous Suzuki–Miyaura cross-coupling reactions - Green Chemistry (RSC Publishing) DOI:10.1039/C4GC00986J](https://pubs.rsc.org/image/article/2014/GC/c4gc00986j/c4gc00986j-s1_hi-res.gif)
Facile-prepared sulfonated water-soluble PEPPSI-Pd-NHC catalysts for aerobic aqueous Suzuki–Miyaura cross-coupling reactions - Green Chemistry (RSC Publishing) DOI:10.1039/C4GC00986J
![Continuous flow Negishi cross-couplings employing silica-supported Pd-PEPPSI – IPr precatalyst - Catalysis Science & Technology (RSC Publishing) DOI:10.1039/C6CY00331A Continuous flow Negishi cross-couplings employing silica-supported Pd-PEPPSI – IPr precatalyst - Catalysis Science & Technology (RSC Publishing) DOI:10.1039/C6CY00331A](https://pubs.rsc.org/image/article/2016/CY/c6cy00331a/c6cy00331a-s3_hi-res.gif)
Continuous flow Negishi cross-couplings employing silica-supported Pd-PEPPSI – IPr precatalyst - Catalysis Science & Technology (RSC Publishing) DOI:10.1039/C6CY00331A
![Benzimidazole bearing Pd–PEPPSI complexes catalyzed direct C2‐arylation/heteroarylation of N‐substituted benzimidazoles - Gokanapalli - - Applied Organometallic Chemistry - Wiley Online Library Benzimidazole bearing Pd–PEPPSI complexes catalyzed direct C2‐arylation/heteroarylation of N‐substituted benzimidazoles - Gokanapalli - - Applied Organometallic Chemistry - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/2051c4b1-f142-447a-b608-c12da2d2d087/aoc5869-fig-0009-m.jpg)
Benzimidazole bearing Pd–PEPPSI complexes catalyzed direct C2‐arylation/heteroarylation of N‐substituted benzimidazoles - Gokanapalli - - Applied Organometallic Chemistry - Wiley Online Library
![PEPPSI‐Type Palladium–NHC Complexes: Synthesis, Characterization, and Catalytic Activity in the Direct C5‐Arylation of 2‐Substituted Thiophene Derivatives with Aryl Halides - Kaloğlu - 2017 - European Journal of Inorganic Chemistry - Wiley Online Library PEPPSI‐Type Palladium–NHC Complexes: Synthesis, Characterization, and Catalytic Activity in the Direct C5‐Arylation of 2‐Substituted Thiophene Derivatives with Aryl Halides - Kaloğlu - 2017 - European Journal of Inorganic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/46194d31-3e52-4461-8e9d-3f5023982a2a/ejic201601452-toc-0001-m.jpg)
PEPPSI‐Type Palladium–NHC Complexes: Synthesis, Characterization, and Catalytic Activity in the Direct C5‐Arylation of 2‐Substituted Thiophene Derivatives with Aryl Halides - Kaloğlu - 2017 - European Journal of Inorganic Chemistry - Wiley Online Library
![Catalysts | Free Full-Text | Palladium PEPPSI-IPr Complex Supported on a Calix[8]arene: A New Catalyst for Efficient Suzuki–Miyaura Coupling of Aryl Chlorides | HTML Catalysts | Free Full-Text | Palladium PEPPSI-IPr Complex Supported on a Calix[8]arene: A New Catalyst for Efficient Suzuki–Miyaura Coupling of Aryl Chlorides | HTML](https://www.mdpi.com/catalysts/catalysts-10-01081/article_deploy/html/images/catalysts-10-01081-i003.png)