Home

Výrobní středisko triumfální Nespokojený aminophosphine palladium catalyst házet Konzumovat Sucho

Highly Convenient, Clean, Fast, and Reliable Sonogashira Coupling Reactions  Promoted by Aminophosphine‐Based Pincer Complexes of Palladium Performed  under Additive‐ and Amine‐Free Reaction Conditions - Bolliger - 2009 -  Advanced Synthesis & Catalysis -
Highly Convenient, Clean, Fast, and Reliable Sonogashira Coupling Reactions Promoted by Aminophosphine‐Based Pincer Complexes of Palladium Performed under Additive‐ and Amine‐Free Reaction Conditions - Bolliger - 2009 - Advanced Synthesis & Catalysis -

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

Synthesis, characterization, and application of palladium complexes  containing bis(aminophosphine) ligands
Synthesis, characterization, and application of palladium complexes containing bis(aminophosphine) ligands

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

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

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

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

Mizoroki–Heck reactions catalyzed by palladium dichloro-bis(aminophosphine)  complexes under mild reaction conditions. The importance of ligand  composition on the catalytic activity - Green Chemistry (RSC Publishing)
Mizoroki–Heck reactions catalyzed by palladium dichloro-bis(aminophosphine) complexes under mild reaction conditions. The importance of ligand composition on the catalytic activity - Green Chemistry (RSC Publishing)

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)

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

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

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

CATALYTIC APPLICATIONS OF AMINOPHOSPHINE-PHOSPHINITES - ppt download
CATALYTIC APPLICATIONS OF AMINOPHOSPHINE-PHOSPHINITES - ppt download

Mizoroki-Heck Cross-coupling Reactions Catalyzed by  Dichloro{bis[1,1',1''-(phosphinetriyl)tripiperidine]}palladium Under Mild  Reaction Conditions | Protocol
Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-(phosphinetriyl)tripiperidine]}palladium Under Mild Reaction Conditions | Protocol

Origins of the enantioselectivity of a palladium catalyst with  BINOL–phosphoric acid ligands - Org. Biomol. Chem. - X-MOL
Origins of the enantioselectivity of a palladium catalyst with BINOL–phosphoric acid ligands - Org. Biomol. Chem. - X-MOL

The 1,3‐Diaminobenzene‐Derived Aminophosphine Palladium Pincer Complex  {C6H3[NHP(piperidinyl)2]2Pd(Cl)} – A Highly Active Suzuki–Miyaura Catalyst  with Excellent Functional Group Tolerance - Bolliger - 2010 - Advanced  Synthesis & Catalysis - Wiley ...
The 1,3‐Diaminobenzene‐Derived Aminophosphine Palladium Pincer Complex {C6H3[NHP(piperidinyl)2]2Pd(Cl)} – A Highly Active Suzuki–Miyaura Catalyst with Excellent Functional Group Tolerance - Bolliger - 2010 - Advanced Synthesis & Catalysis - Wiley ...

The 1,3‐Diaminobenzene‐Derived Aminophosphine Palladium Pincer Complex  {C6H3[NHP(piperidinyl)2]2Pd(Cl)} – A Highly Active Suzuki–Miyaura Catalyst  with Excellent Functional Group Tolerance - Bolliger - 2010 - Advanced  Synthesis & Catalysis - Wiley ...
The 1,3‐Diaminobenzene‐Derived Aminophosphine Palladium Pincer Complex {C6H3[NHP(piperidinyl)2]2Pd(Cl)} – A Highly Active Suzuki–Miyaura Catalyst with Excellent Functional Group Tolerance - Bolliger - 2010 - Advanced Synthesis & Catalysis - Wiley ...

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

PDF) Aminophosphine ligands: Synthesis, coordination chemistry, and  activity of their palladium(II) complexes in Heck and Suzuki cross-coupling  reactions
PDF) Aminophosphine ligands: Synthesis, coordination chemistry, and activity of their palladium(II) complexes in Heck and Suzuki cross-coupling reactions

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

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

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

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

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

Rh-Catalyzed Asymmetric Hydrogenation of (Z)-β-Phosphorylated Enamides:  Highly Enantioselective Access to β-Aminophosphines. - Org. Lett. - X-MOL
Rh-Catalyzed Asymmetric Hydrogenation of (Z)-β-Phosphorylated Enamides: Highly Enantioselective Access to β-Aminophosphines. - Org. Lett. - X-MOL