Pd(PEPPSI)(SIPr) | Precious Metals Chemistry
Benzimidazole bearing Pd–PEPPSI complexes catalyzed direct C2‐arylation/heteroarylation of N‐substituted benzimidazoles - Gokanapalli - - Applied Organometallic 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](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) 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
Dimetallic Palladium‐NHC Complexes: Synthesis, Characterization, and Catalytic Application for Direct C−H Arylation Reaction of Heteroaromatics with Aryl Chlorides - Lee - 2020 - Advanced Synthesis & Catalysis - Wiley Online Library
PDF) Kinetic Study of the Herrmann–Beller Palladacycle-Catalyzed Suzuki–Miyaura Coupling of 4-Iodoacetophenone and Phenylboronic Acid
PDF) Kinetic Study of the Herrmann–Beller Palladacycle-Catalyzed Suzuki–Miyaura Coupling of 4-Iodoacetophenone and Phenylboronic Acid
Adamantanyl-substituted PEPPSI-type palladium(II) N-heterocyclic carbene complexes: synthesis and catalytic application for CH activation of substituted thiophenes | SpringerLink
Investigation of activity, stability, and degradation mechanism of surface-supported Pd-PEPPSI complexes for Suzuki-Miyaura coupling - ScienceDirect
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
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
PEPPSI-Pd-NHC catalyzed Suzuki-Miyaura cross-coupling reactions in aqueous media - ScienceDirect
N‐Heterocyclic carbene) ion‐pair palladium complexes: Suzuki–Miyaura cross‐coupling studies in neat water under mild conditions - Appl. Organomet. Chem. - X-MOL
Cycloheptyl substituted N-heterocyclic carbene PEPPSI-type palladium complexes with different N-coordinated ligands: Involvement in Suzuki-Miyaura reaction - ScienceDirect
Polytriarylamines Containing Fused Ring and Heterocyclic Structures Prepared Using -Heterocyclic Carbene Complexes of Palladium
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
Synergy between supported ionic liquid-like phases and immobilized palladium N-heterocyclic carbene–phosphine complexes for the Negishi reaction under flow conditions
PDF) Kinetic Study of the Herrmann–Beller Palladacycle-Catalyzed Suzuki–Miyaura Coupling of 4-Iodoacetophenone and Phenylboronic Acid
Pd‐PEPPSI‐IPent‐SiO2: A Supported Catalyst for Challenging Negishi Coupling Reactions in Flow - Price - 2017 - Angewandte Chemie International Edition - Wiley Online Library
Pd(PEPPSI)IPr | Precious Metals Chemistry
Continuous flow Negishi cross-couplings employing silica-supported Pd-PEPPSI – IPr precatalyst - Catalysis Science & Technology (RSC Publishing) DOI:10.1039/C6CY00331A
Synthesis of bridged palladium-PEPPSI complexes and catalytic studies in C–C cross-coupling reactions - ScienceDirect
Pd(PEPPSI)IPr | Precious Metals Chemistry
