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Locker prítomný odpustiť palladium trifurylphosphine spleť labyrint Most

Palladium‐Catalyzed Heteroarylation and Concomitant ortho‐Alkylation of  Aryl Iodides - Lei - 2015 - Angewandte Chemie International Edition - Wiley  Online Library
Palladium‐Catalyzed Heteroarylation and Concomitant ortho‐Alkylation of Aryl Iodides - Lei - 2015 - Angewandte Chemie International Edition - Wiley Online Library

Functional Group Transposition: A Palladium-Catalyzed Metathesis of Ar–X  σ-Bonds and Acid Chloride Synthesis | Journal of the American Chemical  Society
Functional Group Transposition: A Palladium-Catalyzed Metathesis of Ar–X σ-Bonds and Acid Chloride Synthesis | Journal of the American Chemical Society

Palladium-Catalyzed Monoarylation of Arylhydrazines with Aryl Tosylates |  The Journal of Organic Chemistry
Palladium-Catalyzed Monoarylation of Arylhydrazines with Aryl Tosylates | The Journal of Organic Chemistry

Transition‐metal‐catalyzed Heteroannulation Reactions in Aqueous Medium -  Dawood - 2022 - Asian Journal of Organic Chemistry - Wiley Online Library
Transition‐metal‐catalyzed Heteroannulation Reactions in Aqueous Medium - Dawood - 2022 - Asian Journal of Organic Chemistry - Wiley Online Library

Efficient and selective Palladium‐catalyzed Telomerization of 1,3‐Butadiene  with Carbon Dioxide - Sharif - 2017 - ChemCatChem - Wiley Online Library
Efficient and selective Palladium‐catalyzed Telomerization of 1,3‐Butadiene with Carbon Dioxide - Sharif - 2017 - ChemCatChem - Wiley Online Library

PDF) Palladium-catalysed reactions in solid phase organic synthesis |  Johannes Köbberling - Academia.edu
PDF) Palladium-catalysed reactions in solid phase organic synthesis | Johannes Köbberling - Academia.edu

Use of a bulky phosphine of weak σ-donicity with palladium as a versatile  and highly-active catalytic system: allylation and arylation coupling  reactions at 10−1–10−4 mol% catalyst loadings of ferrocenyl  bis(difurylphosphine)/Pd - ScienceDirect
Use of a bulky phosphine of weak σ-donicity with palladium as a versatile and highly-active catalytic system: allylation and arylation coupling reactions at 10−1–10−4 mol% catalyst loadings of ferrocenyl bis(difurylphosphine)/Pd - ScienceDirect

Cationic palladium( ii )-indenyl complexes bearing phosphines as ancillary  ligands: synthesis, and study of indenyl amination and anticancer activity  ... - Dalton Transactions (RSC Publishing) DOI:10.1039/D2DT01821G
Cationic palladium( ii )-indenyl complexes bearing phosphines as ancillary ligands: synthesis, and study of indenyl amination and anticancer activity ... - Dalton Transactions (RSC Publishing) DOI:10.1039/D2DT01821G

Tri(2-furyl)phosphine | C12H9O3P - PubChem
Tri(2-furyl)phosphine | C12H9O3P - PubChem

Of the Ortho Effect in Palladium/Norbornene-Catalyzed Reactions: A  Theoretical Investigation | Journal of the American Chemical Society
Of the Ortho Effect in Palladium/Norbornene-Catalyzed Reactions: A Theoretical Investigation | Journal of the American Chemical Society

Functional Group Transposition: A Palladium-Catalyzed Metathesis of Ar–X  σ-Bonds and Acid Chloride Synthesis | Journal of the American Chemical  Society
Functional Group Transposition: A Palladium-Catalyzed Metathesis of Ar–X σ-Bonds and Acid Chloride Synthesis | Journal of the American Chemical Society

Tri(2-furyl)phosphine 5518-52-5 | TCI AMERICA
Tri(2-furyl)phosphine 5518-52-5 | TCI AMERICA

Palladium catalysed cyclisation– carbonylation of enynes to give cyclic  γ,δ-unsaturated acids - Chemical Communications (RSC Publishing)  DOI:10.1039/B300719G
Palladium catalysed cyclisation– carbonylation of enynes to give cyclic γ,δ-unsaturated acids - Chemical Communications (RSC Publishing) DOI:10.1039/B300719G

Linear Triphosphines as Ligands for Metal Complexes Immobilization in Ionic  Liquids: Palladium-Catalyzed Methoxylation of Alkyne
Linear Triphosphines as Ligands for Metal Complexes Immobilization in Ionic Liquids: Palladium-Catalyzed Methoxylation of Alkyne

Palladium catalysed cyclisation– carbonylation of enynes to give cyclic  γ,δ-unsaturated acids - Chemical Communications (RSC Publishing)  DOI:10.1039/B300719G
Palladium catalysed cyclisation– carbonylation of enynes to give cyclic γ,δ-unsaturated acids - Chemical Communications (RSC Publishing) DOI:10.1039/B300719G

Cationic palladium( ii )-indenyl complexes bearing phosphines as ancillary  ligands: synthesis, and study of indenyl amination and anticancer activity  ... - Dalton Transactions (RSC Publishing) DOI:10.1039/D2DT01821G
Cationic palladium( ii )-indenyl complexes bearing phosphines as ancillary ligands: synthesis, and study of indenyl amination and anticancer activity ... - Dalton Transactions (RSC Publishing) DOI:10.1039/D2DT01821G

Applied Sciences | Free Full-Text | Arylation Reactions in the Synthesis of  Biologically Important 2,5-Diaryl-1,3,4-Oxadiazoles
Applied Sciences | Free Full-Text | Arylation Reactions in the Synthesis of Biologically Important 2,5-Diaryl-1,3,4-Oxadiazoles

Selective Ortho Thiolation Enabled by Tuning the Ancillary Ligand in  Palladium/Norbornene Catalysis | Organic Letters
Selective Ortho Thiolation Enabled by Tuning the Ancillary Ligand in Palladium/Norbornene Catalysis | Organic Letters

Of the Ortho Effect in Palladium/Norbornene-Catalyzed Reactions: A  Theoretical Investigation | Journal of the American Chemical Society
Of the Ortho Effect in Palladium/Norbornene-Catalyzed Reactions: A Theoretical Investigation | Journal of the American Chemical Society

Cationic palladium( ii )-indenyl complexes bearing phosphines as ancillary  ligands: synthesis, and study of indenyl amination and anticancer activity  ... - Dalton Transactions (RSC Publishing) DOI:10.1039/D2DT01821G
Cationic palladium( ii )-indenyl complexes bearing phosphines as ancillary ligands: synthesis, and study of indenyl amination and anticancer activity ... - Dalton Transactions (RSC Publishing) DOI:10.1039/D2DT01821G

Palladium- and Copper-Catalyzed Aryl Halide Amination ...
Palladium- and Copper-Catalyzed Aryl Halide Amination ...

Iminophosphine–palladium(0) complexes as catalysts for the Stille reaction  - ScienceDirect
Iminophosphine–palladium(0) complexes as catalysts for the Stille reaction - ScienceDirect

Palladium-Catalyzed Heck-type Domino Cyclization and Carboxylation to  Synthesize Carboxylic Acids by Utilizing Chloroform as the Carbon Monoxide  Source
Palladium-Catalyzed Heck-type Domino Cyclization and Carboxylation to Synthesize Carboxylic Acids by Utilizing Chloroform as the Carbon Monoxide Source

Synthesis of Diverse Heterocyclic Scaffolds by (3+3) and (3+4)  Cycloannulations of Donor‐Acceptor Vinylcyclopropanes
Synthesis of Diverse Heterocyclic Scaffolds by (3+3) and (3+4) Cycloannulations of Donor‐Acceptor Vinylcyclopropanes

Homogeneous and Heterogeneous Pd-Catalyzed Selective C–P Activation and  Transfer Hydrogenation for “Group-Substitution” Synthesis of Trivalent  Phosphines | Organic Letters
Homogeneous and Heterogeneous Pd-Catalyzed Selective C–P Activation and Transfer Hydrogenation for “Group-Substitution” Synthesis of Trivalent Phosphines | Organic Letters

2-Phosphinoimidazole Ligands: N–H NHC or P–N Coordination Complexes in  Palladium-Catalyzed Suzuki–Miyaura Reactions of Aryl Chlorides |  Organometallics
2-Phosphinoimidazole Ligands: N–H NHC or P–N Coordination Complexes in Palladium-Catalyzed Suzuki–Miyaura Reactions of Aryl Chlorides | Organometallics

Cationic palladium( ii )-indenyl complexes bearing phosphines as ancillary  ligands: synthesis, and study of indenyl amination and anticancer activity  ... - Dalton Transactions (RSC Publishing) DOI:10.1039/D2DT01821G
Cationic palladium( ii )-indenyl complexes bearing phosphines as ancillary ligands: synthesis, and study of indenyl amination and anticancer activity ... - Dalton Transactions (RSC Publishing) DOI:10.1039/D2DT01821G

Sterically demanding trialkylphosphines for palladium -catalyzed cross  coupling reactions—alternatives to PtBu3 - Chemical Society Reviews (RSC  Publishing) DOI:10.1039/B903646F
Sterically demanding trialkylphosphines for palladium -catalyzed cross coupling reactions—alternatives to PtBu3 - Chemical Society Reviews (RSC Publishing) DOI:10.1039/B903646F