![Scheme 1 | Dinuclear NHC–palladium(II) complexes: synthesis,characterization and application to Suzuki–Miyaura cross-coupling reactions | SpringerLink Scheme 1 | Dinuclear NHC–palladium(II) complexes: synthesis,characterization and application to Suzuki–Miyaura cross-coupling reactions | SpringerLink](https://media.springernature.com/full/springer-static/image/art%3A10.1007%2Fs11243-018-0224-6/MediaObjects/11243_2018_224_Sch1_HTML.gif)
Scheme 1 | Dinuclear NHC–palladium(II) complexes: synthesis,characterization and application to Suzuki–Miyaura cross-coupling reactions | SpringerLink
![EP2800746B1 - Process for the manufacture of 1-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]-piperazine - Google Patents EP2800746B1 - Process for the manufacture of 1-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]-piperazine - Google Patents](https://patentimages.storage.googleapis.com/0a/c0/98/435d1a40b7cf08/imgb0013.png)
EP2800746B1 - Process for the manufacture of 1-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]-piperazine - Google Patents
![Palladium supported on modified magnetic nanoparticles: a phosphine‐free and heterogeneous catalyst for Suzuki and Stille reactions - Ghorbani‐Choghamarani - 2016 - Applied Organometallic Chemistry - Wiley Online Library Palladium supported on modified magnetic nanoparticles: a phosphine‐free and heterogeneous catalyst for Suzuki and Stille reactions - Ghorbani‐Choghamarani - 2016 - Applied Organometallic Chemistry - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/09c115b5-b585-423b-9c1b-0c8ba1e095d2/aoc3409-fig-0008-m.jpg)
Palladium supported on modified magnetic nanoparticles: a phosphine‐free and heterogeneous catalyst for Suzuki and Stille reactions - Ghorbani‐Choghamarani - 2016 - Applied Organometallic Chemistry - Wiley Online Library
Kinetics and mechanism of the substitution behaviour of Pd(ii) piperazine complexes with different biologically relevant nucleophiles - Dalton Transactions (RSC Publishing)
![Recent progress toward the asymmetric synthesis of carbon-substituted piperazine pharmacophores and oxidative related heterocycles - RSC Medicinal Chemistry (RSC Publishing) DOI:10.1039/D0MD00053A Recent progress toward the asymmetric synthesis of carbon-substituted piperazine pharmacophores and oxidative related heterocycles - RSC Medicinal Chemistry (RSC Publishing) DOI:10.1039/D0MD00053A](https://pubs.rsc.org/image/article/2020/MD/d0md00053a/d0md00053a-s6_hi-res.gif)
Recent progress toward the asymmetric synthesis of carbon-substituted piperazine pharmacophores and oxidative related heterocycles - RSC Medicinal Chemistry (RSC Publishing) DOI:10.1039/D0MD00053A
![Modification of silica using piperazine for immobilization of palladium nanoparticles: a study of its catalytic activity as an efficient heterogeneous catalyst for Heck and Suzuki reactions | SpringerLink Modification of silica using piperazine for immobilization of palladium nanoparticles: a study of its catalytic activity as an efficient heterogeneous catalyst for Heck and Suzuki reactions | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs13738-012-0188-y/MediaObjects/13738_2012_188_Sch1_HTML.gif)
Modification of silica using piperazine for immobilization of palladium nanoparticles: a study of its catalytic activity as an efficient heterogeneous catalyst for Heck and Suzuki reactions | SpringerLink
![Palladium( ii ) induced complete conformational enrichment of the syn isomer of N , N ′-bis(4-pyridylformyl)piperazine - RSC Advances (RSC Publishing) DOI:10.1039/C3RA47904H Palladium( ii ) induced complete conformational enrichment of the syn isomer of N , N ′-bis(4-pyridylformyl)piperazine - RSC Advances (RSC Publishing) DOI:10.1039/C3RA47904H](https://pubs.rsc.org/image/article/2014/RA/c3ra47904h/c3ra47904h-f1_hi-res.gif)
Palladium( ii ) induced complete conformational enrichment of the syn isomer of N , N ′-bis(4-pyridylformyl)piperazine - RSC Advances (RSC Publishing) DOI:10.1039/C3RA47904H
![Modification of silica using piperazine for immobilization of palladium nanoparticles: a study of its catalytic activity as an efficient heterogeneous catalyst for Heck and Suzuki reactions | SpringerLink Modification of silica using piperazine for immobilization of palladium nanoparticles: a study of its catalytic activity as an efficient heterogeneous catalyst for Heck and Suzuki reactions | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs13738-012-0188-y/MediaObjects/13738_2012_188_Figa_HTML.gif)
Modification of silica using piperazine for immobilization of palladium nanoparticles: a study of its catalytic activity as an efficient heterogeneous catalyst for Heck and Suzuki reactions | SpringerLink
![Synthesis of N-arylpiperazines from aryl halides and piperazine under a palladium tri-tert-butylphosphine catalyst - ScienceDirect Synthesis of N-arylpiperazines from aryl halides and piperazine under a palladium tri-tert-butylphosphine catalyst - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040403997106591-gr1.gif)
Synthesis of N-arylpiperazines from aryl halides and piperazine under a palladium tri-tert-butylphosphine catalyst - ScienceDirect
Palladium(ii) induced complete conformational enrichment of the syn isomer of N,N′-bis(4-pyridylformyl)piperazine - RSC Advances (RSC Publishing)
![Recent progress toward the asymmetric synthesis of carbon-substituted piperazine pharmacophores and oxidative related heterocycles - RSC Medicinal Chemistry (RSC Publishing) DOI:10.1039/D0MD00053A Recent progress toward the asymmetric synthesis of carbon-substituted piperazine pharmacophores and oxidative related heterocycles - RSC Medicinal Chemistry (RSC Publishing) DOI:10.1039/D0MD00053A](https://pubs.rsc.org/image/article/2020/MD/d0md00053a/d0md00053a-s11_hi-res.gif)
Recent progress toward the asymmetric synthesis of carbon-substituted piperazine pharmacophores and oxidative related heterocycles - RSC Medicinal Chemistry (RSC Publishing) DOI:10.1039/D0MD00053A
Dichloromethane;diphenylphosphanylmethyl(diphenyl)phosphane;ethoxyethane; palladium(2+);piperazine-1,4-dicarbodithioate;ruthenium(2+);triphenylphosphane;ditetrafluoroborate | C99H98B2Cl6F8N2OP6PdRuS4 - PubChem
![Piperazine as an Inexpensive and Efficient Ligand for Pd-Catalyzed Homocoupling Reactions to Synthesize Bipyridines and Their Analogues | Bentham Science Piperazine as an Inexpensive and Efficient Ligand for Pd-Catalyzed Homocoupling Reactions to Synthesize Bipyridines and Their Analogues | Bentham Science](https://www.eurekaselect.com/images/graphical-abstract/cos/16/1/013.jpg)
Piperazine as an Inexpensive and Efficient Ligand for Pd-Catalyzed Homocoupling Reactions to Synthesize Bipyridines and Their Analogues | Bentham Science
![A practical chromatography-free synthesis of a 5,6-dihydroimidazolo[1,5-f]pteridine derivative as a polo-like kinase-1 inhibitor - Tetrahedron - X-MOL A practical chromatography-free synthesis of a 5,6-dihydroimidazolo[1,5-f]pteridine derivative as a polo-like kinase-1 inhibitor - Tetrahedron - X-MOL](https://xpic.x-mol.com/20180817%2F10.1016_j.tet.2018.08.020.jpg)
A practical chromatography-free synthesis of a 5,6-dihydroimidazolo[1,5-f]pteridine derivative as a polo-like kinase-1 inhibitor - Tetrahedron - X-MOL
![Synthesis of 2,6-Disubstituted Piperazines by a Diastereoselective Palladium-Catalyzed Hydroamination Reaction Synthesis of 2,6-Disubstituted Piperazines by a Diastereoselective Palladium-Catalyzed Hydroamination Reaction](https://www.organic-chemistry.org/abstracts/lit2/015m.gif)
Synthesis of 2,6-Disubstituted Piperazines by a Diastereoselective Palladium-Catalyzed Hydroamination Reaction
![Table 2 from Kinetics and mechanism for the substitution reactions of monoaquamonochloro-(piperazine) palladium (II) complex with L-methionine and thiourea in aqueous solution | Semantic Scholar Table 2 from Kinetics and mechanism for the substitution reactions of monoaquamonochloro-(piperazine) palladium (II) complex with L-methionine and thiourea in aqueous solution | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/0a7374c66cfd7d4c5be907d4330fb6b328fff971/3-Table3-1.png)
Table 2 from Kinetics and mechanism for the substitution reactions of monoaquamonochloro-(piperazine) palladium (II) complex with L-methionine and thiourea in aqueous solution | Semantic Scholar
![EP2800746B1 - Process for the manufacture of 1-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]-piperazine - Google Patents EP2800746B1 - Process for the manufacture of 1-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]-piperazine - Google Patents](https://patentimages.storage.googleapis.com/53/5f/9b/46ea6342cf2651/imgb0001.png)
EP2800746B1 - Process for the manufacture of 1-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]-piperazine - Google Patents
![Synthesis of arylpiperazines via palladium-catalyzed aromatic amination reaction with unprotected piperazines - ScienceDirect Synthesis of arylpiperazines via palladium-catalyzed aromatic amination reaction with unprotected piperazines - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-0040403996008775-fx1.gif)
Synthesis of arylpiperazines via palladium-catalyzed aromatic amination reaction with unprotected piperazines - ScienceDirect
![Pd-Catalyzed Synthesis of Piperazine Scaffolds Under Aerobic and Solvent-Free Conditions. - Abstract - Europe PMC Pd-Catalyzed Synthesis of Piperazine Scaffolds Under Aerobic and Solvent-Free Conditions. - Abstract - Europe PMC](https://europepmc.org/articles/PMC5984194/bin/nihms968206f4.jpg)
Pd-Catalyzed Synthesis of Piperazine Scaffolds Under Aerobic and Solvent-Free Conditions. - Abstract - Europe PMC
![Recent progress toward the asymmetric synthesis of carbon-substituted piperazine pharmacophores and oxidative related heterocycles - RSC Medicinal Chemistry (RSC Publishing) DOI:10.1039/D0MD00053A Recent progress toward the asymmetric synthesis of carbon-substituted piperazine pharmacophores and oxidative related heterocycles - RSC Medicinal Chemistry (RSC Publishing) DOI:10.1039/D0MD00053A](https://pubs.rsc.org/image/article/2020/MD/d0md00053a/d0md00053a-s5_hi-res.gif)
Recent progress toward the asymmetric synthesis of carbon-substituted piperazine pharmacophores and oxidative related heterocycles - RSC Medicinal Chemistry (RSC Publishing) DOI:10.1039/D0MD00053A
![Pd-Catalyzed Synthesis of Piperazine Scaffolds Under Aerobic and Solvent-Free Conditions. - Abstract - Europe PMC Pd-Catalyzed Synthesis of Piperazine Scaffolds Under Aerobic and Solvent-Free Conditions. - Abstract - Europe PMC](https://europepmc.org/articles/PMC5984194/bin/nihms968206u1.jpg)