Camphane-based aminophosphine ligands for Pd-catalyzed asymmetric allylic alkylation - ScienceDirect
The effect of ligand composition of... | Download Scientific Diagram
CATALYTIC APPLICATIONS OF AMINOPHOSPHINE-PHOSPHINITES - ppt download
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
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, characterization, and application of palladium complexes containing bis(aminophosphine) ligands
Synthesis of platinum, palladium and rhodium complexes of α-aminophosphine ligands - Dalton Transactions (RSC Publishing) DOI:10.1039/C8DT00178B
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 -
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
Multifunctional chiral aminophosphines for enantiodivergent catalysis in a palladium‐catalyzed allylic alkylation reaction - Eliseenko - 2020 - Chirality - Wiley Online Library
![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](https://ars.els-cdn.com/content/image/1-s2.0-S0022328X07001738-fx1.jpg "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, 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
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
Synthesis of platinum, palladium and rhodium complexes of α-aminophosphine ligands - Dalton Transactions (RSC Publishing) DOI:10.1039/C8DT00178B
![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 ...")
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
Proposed mechanism for the palladium pincer-catalyzed carbonylative... | Download Scientific Diagram
Synthesis of platinum, palladium and rhodium complexes of α-aminophosphine ligands - Dalton Transactions (RSC Publishing) DOI:10.1039/C8DT00178B
![Preparation and Application of Amino Phosphine Ligands Bearing Spiro[indane-1,2′-pyrrolidine] Backbone - J. Org. Chem. - X-MOL](https://xpic.x-mol.com/20190712%2F10.1021_acs.joc.9b00875.jpg "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
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
Rh-Catalyzed Asymmetric Hydrogenation of (Z)-β-Phosphorylated Enamides: Highly Enantioselective Access to β-Aminophosphines. - Org. Lett. - X-MOL
