![Various [NHC-Pd-PEPPSI] (left) and long alkyl chain-labeled... | Download Scientific Diagram](https://www.researchgate.net/profile/Muhammad_Ghufran_Rafique/publication/317660984/figure/fig1/AS:528262394638337@1502958977918/Various-NHC-Pd-PEPPSI-left-and-long-alkyl-chain-labeled-NHC-Pdallyl-cinnamyl.png "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
![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-g001.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")
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
Amino acid-derived N-heterocyclic carbene palladium complexes for aqueous phase Suzuki–Miyaura couplings - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C5NJ03337C
PEPPSI™ Catalyst | Sigma-Aldrich
Pd(PEPPSI)(SIPr) | Precious Metals Chemistry
Figure 1 from PEPPSI-type palladium complexes containing basic 1,2,3-triazolylidene ligands and their role in Suzuki-Miyaura catalysis. | Semantic Scholar
The Development of Bulky Palladium NHC Complexes for the Most-Challen…
Overview of the Ligand Precursors Used for the Preparation of Pd-PEPPSI... | Download Table
PEPPSI™ Catalysts in Chemical Synthesis | Sigma-Aldrich
Adamantanyl-substituted PEPPSI-type palladium(II) N-heterocyclic carbene complexes: synthesis and catalytic application for CH activation of substituted thiophenes | SpringerLink
Synthesis of N-heterocyclic carbene-palladium-PEPPSI complexes and their catalytic activity in the direct C-H bond activation - ScienceDirect
Pd‐PEPPSI Complexes and the Negishi Reaction - Valente - 2010 - European Journal of Organic Chemistry - Wiley Online Library
Pd(PEPPSI)IPr | Cobalt & Specialty Materials
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‐IHeptCl: A General‐Purpose, Highly Reactive Catalyst for the Selective Coupling of Secondary Alkyl Organozincs - Chem. Eur. J. - X-MOL
PEPPSI™-IPent for Demanding Cross-Coupling Reactions | Sigma-Aldrich
1 H-NMR spectra of palladium PEPPSI-type complex 3a in CDCl3. | Download Scientific Diagram
Pd(PEPPSI)IPr | Cobalt & Specialty Materials
PEPPSI - Wikiwand
Molecules | Free Full-Text | Well-Defined Pre-Catalysts in Amide and Ester Bond Activation | HTML
Cycloheptyl substituted N-heterocyclic carbene PEPPSI-type palladium complexes with different N-coordinated ligands: Involvement in Suzuki-Miyaura reaction - J. Organomet. Chem. - X-MOL
Synthesis, characterization and catalytic activity of PEPPSI-type palladium–NHC complexes - ScienceDirect
PEPPSI - Wikiwand
Pd-PEPPSI™-IPent catalyst >= 95 % | 1158652-41-5 | Sigma-Aldrich
PEPPSI - Wikipedia
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
PDF) Phase-Separable Polyisobutylene Palladium-PEPPSI Precatalysts: Synthesis and Application in Buchwald– Hartwig Amination
