![Catalysts | Free Full-Text | N-Acylphthalimides: Efficient Acyl Coupling Reagents in Suzuki–Miyaura Cross-Coupling by N–C Cleavage Catalyzed by Pd– PEPPSI Precatalysts | HTML Catalysts | Free Full-Text | N-Acylphthalimides: Efficient Acyl Coupling Reagents in Suzuki–Miyaura Cross-Coupling by N–C Cleavage Catalyzed by Pd– PEPPSI Precatalysts | HTML](https://www.mdpi.com/catalysts/catalysts-09-00129/article_deploy/html/images/catalysts-09-00129-sch005.png)
Catalysts | Free Full-Text | N-Acylphthalimides: Efficient Acyl Coupling Reagents in Suzuki–Miyaura Cross-Coupling by N–C Cleavage Catalyzed by Pd– PEPPSI Precatalysts | HTML
![Catalysts | Free Full-Text | An Amino-Chain Modified β-cyclodextrin: A Supramolecular Ligand for Pd(OAc)2 Acceleration in Suzuki–Miyaura Coupling Reactions in Water Catalysts | Free Full-Text | An Amino-Chain Modified β-cyclodextrin: A Supramolecular Ligand for Pd(OAc)2 Acceleration in Suzuki–Miyaura Coupling Reactions in Water](https://www.mdpi.com/catalysts/catalysts-09-00111/article_deploy/html/images/catalysts-09-00111-ag.png)
Catalysts | Free Full-Text | An Amino-Chain Modified β-cyclodextrin: A Supramolecular Ligand for Pd(OAc)2 Acceleration in Suzuki–Miyaura Coupling Reactions in Water
![An Alternative Approach to PEPPSI Catalysts: From Palladium Isonitriles to Highly Active Unsymmetrically Substituted PEPPSI Catalysts - Chem. Eur. J. - X-MOL An Alternative Approach to PEPPSI Catalysts: From Palladium Isonitriles to Highly Active Unsymmetrically Substituted PEPPSI Catalysts - Chem. Eur. J. - X-MOL](https://xpic.x-mol.com/thesis%2FChemistry_-_A_European_Journal%2F21d41bfab0a71984d868979901990a028ac5d8e6.gif)
An Alternative Approach to PEPPSI Catalysts: From Palladium Isonitriles to Highly Active Unsymmetrically Substituted PEPPSI Catalysts - Chem. Eur. J. - X-MOL
![Pd‐PEPPSI: Water‐Assisted Suzuki−Miyaura Cross‐Coupling of Aryl Esters at Room Temperature using a Practical Palladium‐NHC (NHC=N‐Heterocyclic Carbene) Precatalyst - Li - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library Pd‐PEPPSI: Water‐Assisted Suzuki−Miyaura Cross‐Coupling of Aryl Esters at Room Temperature using a Practical Palladium‐NHC (NHC=N‐Heterocyclic Carbene) Precatalyst - Li - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/e3c0d84d-65fc-4cd9-b9a1-8107bb38aedf/adsc201701563-toc-0001-m.jpg)
Pd‐PEPPSI: Water‐Assisted Suzuki−Miyaura Cross‐Coupling of Aryl Esters at Room Temperature using a Practical Palladium‐NHC (NHC=N‐Heterocyclic Carbene) Precatalyst - Li - 2018 - Advanced Synthesis & Catalysis - 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
![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
![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_Fig1_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
![Figure 1 from PEPPSI-type palladium complexes containing basic 1,2,3-triazolylidene ligands and their role in Suzuki-Miyaura catalysis. | Semantic Scholar Figure 1 from PEPPSI-type palladium complexes containing basic 1,2,3-triazolylidene ligands and their role in Suzuki-Miyaura catalysis. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/bcafbe65d20a262af0dfe0630d660caec3c683f8/2-Figure1-1.png)
Figure 1 from PEPPSI-type palladium complexes containing basic 1,2,3-triazolylidene ligands and their role in Suzuki-Miyaura catalysis. | Semantic Scholar
![Pd-PEPPSI-IPentCl: a new highly efficient ligand-free and recyclable catalyst system for the synthesis of 2-substituted indoles via domino copper-free Sonogashira coupling/cyclization - New Journal of Chemistry (RSC Publishing) Pd-PEPPSI-IPentCl: a new highly efficient ligand-free and recyclable catalyst system for the synthesis of 2-substituted indoles via domino copper-free Sonogashira coupling/cyclization - New Journal of Chemistry (RSC Publishing)](https://pubs.rsc.org/image/article/2017/nj/c7nj01544e/c7nj01544e-s1_hi-res.gif)