![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](https://onlinelibrary.wiley.com/cms/asset/ebe55b7d-b0aa-41a7-aa82-bc643d9cdf32/chir23275-toc-0001-m.jpg)
Multifunctional chiral aminophosphines for enantiodivergent catalysis in a palladium‐catalyzed allylic alkylation reaction - Eliseenko - 2020 - Chirality - Wiley Online Library
![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](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
![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 ...](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 ...
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)
![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](https://xpic.x-mol.com/20190119%2F10.1021_acsomega.8b02886.jpg)
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. - Abstract - Europe PMC Aminophosphine Palladium Pincer-Catalyzed Carbonylative Sonogashira and Suzuki-Miyaura Cross-Coupling with High Catalytic Turnovers. - Abstract - Europe PMC](https://europepmc.org/articles/PMC6648871/bin/ao-2018-02886p_0007.jpg)
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 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](https://d3i71xaburhd42.cloudfront.net/6c0cfca2b6178b0b718c8ffd5b7ae90bcb200940/9-Table1-1.png)
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](https://i1.rgstatic.net/publication/251353746_Aminophosphine_ligands_Synthesis_coordination_chemistry_and_activity_of_their_palladiumII_complexes_in_Heck_and_Suzuki_cross-coupling_reactions/links/02e7e538985c7b82b7000000/largepreview.png)
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](https://pubs.rsc.org/image/article/2018/DT/c8dt00178b/c8dt00178b-s32.gif)
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)
![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](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10562-016-1944-x/MediaObjects/10562_2016_1944_Figa_HTML.gif)
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
![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](https://ars.els-cdn.com/content/image/1-s2.0-S0022328X18307678-fx1.jpg)
Synthesis, structure, computational and catalytic activities of palladium complexes containing hydrazide based amino-phosphine ligands - 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](https://d3i71xaburhd42.cloudfront.net/6c0cfca2b6178b0b718c8ffd5b7ae90bcb200940/6-Figure3-1.png)
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
![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](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/a177f7a6-d79c-494a-a4dc-f46e87d38a43/mcontent.jpg)
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
![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](https://ars.els-cdn.com/content/image/1-s2.0-S0022328X20303156-gr2.jpg)
Cationic palladium(II)–acetylacetonate complexes containing phosphine and aminophosphine ligands and their catalytic activities in telomerization of 1,3-butadiene with methanol - 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](https://europepmc.org/articles/PMC6648871/bin/ao-2018-02886p_0011.jpg)
Aminophosphine Palladium Pincer-Catalyzed Carbonylative Sonogashira and Suzuki-Miyaura Cross-Coupling with High Catalytic Turnovers. - Abstract - Europe PMC
![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](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
![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](https://xpic.x-mol.com/20200527%2F10.1021_acs.organomet.0c00154.gif)
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
![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](https://xpic.x-mol.com/20191101%2F10.1021_acs.orglett.9b03174.jpg)
Rh-Catalyzed Asymmetric Hydrogenation of (Z)-β-Phosphorylated Enamides: Highly Enantioselective Access to β-Aminophosphines. - Org. Lett. - X-MOL
![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](https://d3i71xaburhd42.cloudfront.net/6c0cfca2b6178b0b718c8ffd5b7ae90bcb200940/6-Figure2-1.png)
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](https://d3i71xaburhd42.cloudfront.net/6c0cfca2b6178b0b718c8ffd5b7ae90bcb200940/10-Table2-1.png)