Home

Saha Uzak toksisite palladium peppsi solubility yenilebilir öncel paralel

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

Synthesis, characterization and catalytic activity of PEPPSI-type palladium–NHC  complexes - ScienceDirect
Synthesis, characterization and catalytic activity of PEPPSI-type palladium–NHC complexes - ScienceDirect

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

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)

PEPPSI-Pd-NHC catalyzed Suzuki-Miyaura cross-coupling reactions in aqueous  media - ScienceDirect
PEPPSI-Pd-NHC catalyzed Suzuki-Miyaura cross-coupling reactions in aqueous media - ScienceDirect

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

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

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

PEPPSI-Pd-NHC catalyzed Suzuki-Miyaura cross-coupling reactions in aqueous  media - ScienceDirect
PEPPSI-Pd-NHC catalyzed Suzuki-Miyaura cross-coupling reactions in aqueous media - ScienceDirect

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

Alternative Synthetic Methods for PEPPSI‐Type Palladium Complexes - Green -  2014 - European Journal of Inorganic Chemistry - Wiley Online Library
Alternative Synthetic Methods for PEPPSI‐Type Palladium Complexes - Green - 2014 - European Journal of Inorganic Chemistry - Wiley Online Library

Continuous flow Negishi cross-couplings employing silica-supported Pd-PEPPSI–IPr  precatalyst - Catalysis Science & Technology (RSC Publishing)
Continuous flow Negishi cross-couplings employing silica-supported Pd-PEPPSI–IPr precatalyst - Catalysis Science & Technology (RSC Publishing)

Well‐defined PEPPSI‐themed palladium–NHC complexes: synthesis, and  catalytic application in the direct arylation of heteroarenes - Kaloğlu -  2020 - Applied Organometallic Chemistry - Wiley Online Library
Well‐defined PEPPSI‐themed palladium–NHC complexes: synthesis, and catalytic application in the direct arylation of heteroarenes - Kaloğlu - 2020 - Applied Organometallic Chemistry - Wiley Online Library

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

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

PDF) PEPPSI-Type Palladium Complexes Containing Basic 1,2,3-Triazolylidene  Ligands and Their Role in Suzuki-Miyaura Catalysis
PDF) PEPPSI-Type Palladium Complexes Containing Basic 1,2,3-Triazolylidene Ligands and Their Role in Suzuki-Miyaura Catalysis

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

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

Recent Advances in the Palladium Catalyzed Suzuki–Miyaura Cross-Coupling  Reaction in Water | SpringerLink
Recent Advances in the Palladium Catalyzed Suzuki–Miyaura Cross-Coupling Reaction in Water | SpringerLink

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
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

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
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

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

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

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

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