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Vysoká expozice Závislost bludiště aminophosphine palladium catalyst hluboký Pat přes

Proposed mechanism for the palladium pincer-catalyzed carbonylative... |  Download Scientific Diagram
Proposed mechanism for the palladium pincer-catalyzed carbonylative... | Download Scientific Diagram

Cationic palladium(II)–acetylacetonate complexes containing phosphine and  aminophosphine ligands and their catalytic activities in telomerization of  1,3-butadiene with methanol - ScienceDirect
Cationic palladium(II)–acetylacetonate complexes containing phosphine and aminophosphine ligands and their catalytic activities in telomerization of 1,3-butadiene with methanol - ScienceDirect

Preparation and Application of Amino Phosphine Ligands Bearing  Spiro[indane-1,2′-pyrrolidine] Backbone - J. Org. Chem. - X-MOL
Preparation and Application of Amino Phosphine Ligands Bearing Spiro[indane-1,2′-pyrrolidine] Backbone - J. Org. Chem. - X-MOL

PDF) Aminophosphine Palladium Pincer-Catalyzed Carbonylative Sonogashira  and Suzuki–Miyaura Cross-Coupling with High Catalytic Turnovers
PDF) Aminophosphine Palladium Pincer-Catalyzed Carbonylative Sonogashira and Suzuki–Miyaura Cross-Coupling with High Catalytic Turnovers

Synthesis, structure, computational and catalytic activities of palladium  complexes containing hydrazide based amino-phosphine ligands - ScienceDirect
Synthesis, structure, computational and catalytic activities of palladium complexes containing hydrazide based amino-phosphine ligands - ScienceDirect

Development of P- and N-Chirogenic Ligands Based on Chiral Induction from a  Phosphorus Donor to a Nitrogen Donor in Palladium Complexes -  Organometallics - X-MOL
Development of P- and N-Chirogenic Ligands Based on Chiral Induction from a Phosphorus Donor to a Nitrogen Donor in Palladium Complexes - Organometallics - X-MOL

Synthesis of platinum, palladium and rhodium complexes of α-aminophosphine  ligands - Dalton Transactions (RSC Publishing) DOI:10.1039/C8DT00178B
Synthesis of platinum, palladium and rhodium complexes of α-aminophosphine ligands - Dalton Transactions (RSC Publishing) DOI:10.1039/C8DT00178B

Synthesis of platinum, palladium and rhodium complexes of α-aminophosphine  ligands - Dalton Transactions (RSC Publishing)
Synthesis of platinum, palladium and rhodium complexes of α-aminophosphine ligands - Dalton Transactions (RSC Publishing)

Aminophosphine Palladium(0) Complex Supported on ZrO 2 Nanoparticles (ZrO 2  @AEPH 2 -PPh 2 -Pd(0)) as an Efficient Heterogeneous Catalyst for  Suzuki–Miyaura and Heck–Mizoroki Reactions in Green Media | SpringerLink
Aminophosphine Palladium(0) Complex Supported on ZrO 2 Nanoparticles (ZrO 2 @AEPH 2 -PPh 2 -Pd(0)) as an Efficient Heterogeneous Catalyst for Suzuki–Miyaura and Heck–Mizoroki Reactions in Green Media | SpringerLink

Aminophosphine Palladium(0) Complex Supported on ZrO2 Nanoparticles  (ZrO2@AEPH2-PPh2-Pd(0)) as an Efficient Heterogeneous Catalyst for  Suzuki–Miyaura and Heck–Mizoroki Reactions in Green Media | Request PDF
Aminophosphine Palladium(0) Complex Supported on ZrO2 Nanoparticles (ZrO2@AEPH2-PPh2-Pd(0)) as an Efficient Heterogeneous Catalyst for Suzuki–Miyaura and Heck–Mizoroki Reactions in Green Media | Request PDF

Synthesis of platinum, palladium and rhodium complexes of α-aminophosphine  ligands - Dalton Transactions (RSC Publishing) DOI:10.1039/C8DT00178B
Synthesis of platinum, palladium and rhodium complexes of α-aminophosphine ligands - Dalton Transactions (RSC Publishing) DOI:10.1039/C8DT00178B

Synthesis of platinum, palladium and rhodium complexes of α-aminophosphine  ligands - Dalton Transactions (RSC Publishing) DOI:10.1039/C8DT00178B
Synthesis of platinum, palladium and rhodium complexes of α-aminophosphine ligands - Dalton Transactions (RSC Publishing) DOI:10.1039/C8DT00178B

Aminophosphine complex as a catalyst precursor in Suzuki coupling reactions  | SpringerLink
Aminophosphine complex as a catalyst precursor in Suzuki coupling reactions | SpringerLink

Table 1 from Aminophosphine Palladium(0) Complex Supported on ZrO2  Nanoparticles (ZrO2@AEPH2-PPh2-Pd(0)) as an Efficient Heterogeneous Catalyst  for Suzuki–Miyaura and Heck–Mizoroki Reactions in Green Media | Semantic  Scholar
Table 1 from Aminophosphine Palladium(0) Complex Supported on ZrO2 Nanoparticles (ZrO2@AEPH2-PPh2-Pd(0)) as an Efficient Heterogeneous Catalyst for Suzuki–Miyaura and Heck–Mizoroki Reactions in Green Media | Semantic Scholar

Synthesis and characterization of palladium(II) complexes with chiral  aminophosphine ligands: Catalytic behaviour in asymmetric hydrovinylation.  Crystal structure of cis-[PdCl2(PPh((R)-NHCHCH3Ph)2)2] - ScienceDirect
Synthesis and characterization of palladium(II) complexes with chiral aminophosphine ligands: Catalytic behaviour in asymmetric hydrovinylation. Crystal structure of cis-[PdCl2(PPh((R)-NHCHCH3Ph)2)2] - ScienceDirect

Table 1 from Aminophosphine Palladium(0) Complex Supported on ZrO2  Nanoparticles (ZrO2@AEPH2-PPh2-Pd(0)) as an Efficient Heterogeneous Catalyst  for Suzuki–Miyaura and Heck–Mizoroki Reactions in Green Media | Semantic  Scholar
Table 1 from Aminophosphine Palladium(0) Complex Supported on ZrO2 Nanoparticles (ZrO2@AEPH2-PPh2-Pd(0)) as an Efficient Heterogeneous Catalyst for Suzuki–Miyaura and Heck–Mizoroki Reactions in Green Media | Semantic Scholar

Table 1 from Aminophosphine Palladium(0) Complex Supported on ZrO2  Nanoparticles (ZrO2@AEPH2-PPh2-Pd(0)) as an Efficient Heterogeneous Catalyst  for Suzuki–Miyaura and Heck–Mizoroki Reactions in Green Media | Semantic  Scholar
Table 1 from Aminophosphine Palladium(0) Complex Supported on ZrO2 Nanoparticles (ZrO2@AEPH2-PPh2-Pd(0)) as an Efficient Heterogeneous Catalyst for Suzuki–Miyaura and Heck–Mizoroki Reactions in Green Media | Semantic Scholar

Multifunctional chiral aminophosphines for enantiodivergent catalysis in a  palladium‐catalyzed allylic alkylation reaction - Eliseenko - 2020 -  Chirality - Wiley Online Library
Multifunctional chiral aminophosphines for enantiodivergent catalysis in a palladium‐catalyzed allylic alkylation reaction - Eliseenko - 2020 - Chirality - Wiley Online Library

The effect of ligand composition of... | Download Scientific Diagram
The effect of ligand composition of... | Download Scientific Diagram

PDF) Aminophosphine–palladium(II) complexes: Synthsesis, structure and  applications in Suzuki and Heck cross-coupling reactions | Murat Aydemir -  Academia.edu
PDF) Aminophosphine–palladium(II) complexes: Synthsesis, structure and applications in Suzuki and Heck cross-coupling reactions | Murat Aydemir - Academia.edu

Camphane-based aminophosphine ligands for Pd-catalyzed asymmetric allylic  alkylation - ScienceDirect
Camphane-based aminophosphine ligands for Pd-catalyzed asymmetric allylic alkylation - ScienceDirect

Aminophosphine Palladium Pincer-Catalyzed Carbonylative Sonogashira and  Suzuki-Miyaura Cross-Coupling with High Catalytic Turnovers. - Abstract -  Europe PMC
Aminophosphine Palladium Pincer-Catalyzed Carbonylative Sonogashira and Suzuki-Miyaura Cross-Coupling with High Catalytic Turnovers. - Abstract - Europe PMC

Aminophosphine Palladium Pincer-Catalyzed Carbonylative Sonogashira and  Suzuki–Miyaura Cross-Coupling with High Catalytic Turnovers - ACS Omega -  X-MOL
Aminophosphine Palladium Pincer-Catalyzed Carbonylative Sonogashira and Suzuki–Miyaura Cross-Coupling with High Catalytic Turnovers - ACS Omega - X-MOL

Cationic palladium(II)–acetylacetonate complexes containing phosphine and  aminophosphine ligands and their catalytic activities in telomerization of  1,3-butadiene with methanol - ScienceDirect
Cationic palladium(II)–acetylacetonate complexes containing phosphine and aminophosphine ligands and their catalytic activities in telomerization of 1,3-butadiene with methanol - ScienceDirect

Dichloro‐Bis(aminophosphine) Complexes of Palladium: Highly Convenient,  Reliable and Extremely Active Suzuki–Miyaura Catalysts with Excellent  Functional Group Tolerance - Bolliger - 2010 - Chemistry – A European  Journal - Wiley Online Library
Dichloro‐Bis(aminophosphine) Complexes of Palladium: Highly Convenient, Reliable and Extremely Active Suzuki–Miyaura Catalysts with Excellent Functional Group Tolerance - Bolliger - 2010 - Chemistry – A European Journal - Wiley Online Library