Pd(PEPPSI)IPr | Precious Metals Chemistry
Synergy between supported ionic liquid-like phases and immobilized palladium N-heterocyclic carbene–phosphine complexes for th
![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
PDF) Kinetic Study of the Herrmann–Beller Palladacycle-Catalyzed Suzuki–Miyaura Coupling of 4-Iodoacetophenone and Phenylboronic Acid
Sulfination by Using Pd‐PEPPSI Complexes: Studies into Precatalyst Activation, Cationic and Solvent Effects and the Role of Butoxide Base - Sayah - 2013 - Chemistry – A European Journal - Wiley Online Library
PDF) 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
Synthesis, characterization and catalytic activity of PEPPSI-type palladium–NHC complexes - ScienceDirect
Room‐Temperature Amination of Deactivated Aniline and Aryl Halide Partners with Carbonate Base Using a Pd‐PEPPSI‐IPentCl‐ o‐Picoline Catalyst - Pompeo - 2014 - Angewandte Chemie International Edition - Wiley Online Library
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
PDF) Kinetic Study of the Herrmann–Beller Palladacycle-Catalyzed Suzuki–Miyaura Coupling of 4-Iodoacetophenone and Phenylboronic Acid
Pd‐PEPPSI Complexes and the Negishi Reaction - Valente - 2010 - European Journal of Organic Chemistry - Wiley Online Library
PEPPSI-Pd-NHC catalyzed Suzuki-Miyaura cross-coupling reactions in aqueous media - ScienceDirect
Pd(PEPPSI)(SIPr) | Precious Metals Chemistry
Phase‐Separable Polyisobutylene Palladium‐PEPPSI Precatalysts: Synthesis and Application in Buchwald–Hartwig Amination - Balogh - 2017 - Macromolecular Rapid Communications - Wiley Online Library
Pd(PEPPSI)(SIPr) | Precious Metals Chemistry
Pd(PEPPSI)IPr | Precious Metals Chemistry
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
Pd(PEPPSI)(SIPr) | Precious Metals Chemistry
Pd(PEPPSI)(SIPr) | Precious Metals Chemistry
Synergy between supported ionic liquid-like phases and immobilized palladium N-heterocyclic carbene–phosphine complexes for the Negishi reaction under flow conditions
Synthesis of bridged palladium-PEPPSI complexes and catalytic studies in C–C cross-coupling reactions - ScienceDirect
Pd(PEPPSI)IPr | Precious Metals Chemistry
N‐Heterocyclic carbene) ion‐pair palladium complexes: Suzuki–Miyaura cross‐coupling studies in neat water under mild conditions - Appl. Organomet. Chem. - X-MOL
PDF) Kinetic Study of the Herrmann–Beller Palladacycle-Catalyzed Suzuki–Miyaura Coupling of 4-Iodoacetophenone and Phenylboronic Acid
PDF) Solubility of Palladium (Pd) in Hydrocarbons: Application to Ore Genesis
Polytriarylamines Containing Fused Ring and Heterocyclic Structures Prepared Using -Heterocyclic Carbene Complexes of Palladium
