PDF) Aminophosphine Palladium Pincer-Catalyzed Carbonylative Sonogashira and Suzuki–Miyaura Cross-Coupling with High Catalytic Turnovers
PDF) Aminophosphine–palladium(II) complexes: Synthsesis, structure and applications in Suzuki and Heck cross-coupling reactions | Murat Aydemir - Academia.edu
Rh-Catalyzed Asymmetric Hydrogenation of (Z)-β-Phosphorylated Enamides: Highly Enantioselective Access to β-Aminophosphines. - Org. Lett. - X-MOL
Synthesis of platinum, palladium and rhodium complexes of α-aminophosphine ligands - Dalton Transactions (RSC Publishing) DOI:10.1039/C8DT00178B
CATALYTIC APPLICATIONS OF AMINOPHOSPHINE-PHOSPHINITES - ppt download
Proposed mechanism for the palladium pincer-catalyzed carbonylative... | Download Scientific Diagram
PDF) Aminophosphine ligands: Synthesis, coordination chemistry, and activity of their palladium(II) complexes in Heck and Suzuki cross-coupling reactions
![Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-(phosphinetriyl)tripiperidine]}palladium Under Mild Reaction Conditions | Protocol](https://cloudfront.jove.com/files/ftp_upload/51444/51444fig3.jpg "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
Aminophosphine complex as a catalyst precursor in Suzuki coupling reactions | SpringerLink
Synthesis, characterization, and application of palladium complexes containing bis(aminophosphine) ligands
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
The effect of ligand composition of... | Download Scientific Diagram
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
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)
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 -
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)
Cationic palladium(II)–acetylacetonate complexes containing phosphine and aminophosphine ligands and their catalytic activities in telomerization of 1,3-butadiene with methanol - ScienceDirect
Multifunctional chiral aminophosphines for enantiodivergent catalysis in a palladium‐catalyzed allylic alkylation reaction - Eliseenko - 2020 - Chirality - Wiley Online Library
![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 ...](https://onlinelibrary.wiley.com/cms/asset/16d0c16a-ffaf-4992-b9e6-91a5da65039b/mcontent.jpg "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 ...
Aminophosphine Palladium Pincer-Catalyzed Carbonylative Sonogashira and Suzuki-Miyaura Cross-Coupling with High Catalytic Turnovers. - Abstract - Europe PMC
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
Bis-N,N-aminophosphine (PNP) crosslinked poly(p-tert-butyl styrene) particles: A new support for heterogeneous palladium catalysts for Suzuki coupling reactions - Catal. Commun. - X-MOL
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
![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 ...](https://onlinelibrary.wiley.com/cms/asset/734bf342-fa45-4f08-a712-c34ceb2581a0/msch001.jpg "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 ...")