![Enantioselective synthesis of gem -disubstituted N -Boc diazaheterocycles via decarboxylative asymmetric allylic alkylation - Chemical Science (RSC Publishing) DOI:10.1039/C8SC03967D Enantioselective synthesis of gem -disubstituted N -Boc diazaheterocycles via decarboxylative asymmetric allylic alkylation - Chemical Science (RSC Publishing) DOI:10.1039/C8SC03967D](https://pubs.rsc.org/image/article/2019/SC/c8sc03967d/c8sc03967d-s1_hi-res.gif)
Enantioselective synthesis of gem -disubstituted N -Boc diazaheterocycles via decarboxylative asymmetric allylic alkylation - Chemical Science (RSC Publishing) DOI:10.1039/C8SC03967D
![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
![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
Kinetics and mechanism of the substitution behaviour of Pd(ii) piperazine complexes with different biologically relevant nucleophiles - Dalton Transactions (RSC Publishing)
![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
![Palladium-Catalyzed Modular Synthesis of Substituted Piperazines and Related Nitrogen Heterocycles. - PDF Download Free Palladium-Catalyzed Modular Synthesis of Substituted Piperazines and Related Nitrogen Heterocycles. - PDF Download Free](https://docksci.com/assets/img/docksci_logo.png)
Palladium-Catalyzed Modular Synthesis of Substituted Piperazines and Related Nitrogen Heterocycles. - PDF Download Free
![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
![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
![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
Dichloromethane;diphenylphosphanylmethyl(diphenyl)phosphane;ethoxyethane; palladium(2+);piperazine-1,4-dicarbodithioate;ruthenium(2+);triphenylphosphane;ditetrafluoroborate | C99H98B2Cl6F8N2OP6PdRuS4 - PubChem
![PDF) 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 PDF) 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](https://i1.rgstatic.net/publication/257806872_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/links/5495b74a0cf2ec13375b2bae/largepreview.png)
PDF) 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
![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
![Process for the manufacture of 1-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]- piperazine - US 9,133,144 B2 - PatentSwarm Process for the manufacture of 1-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]- piperazine - US 9,133,144 B2 - PatentSwarm](https://images.patentswarm.com/US9133144B2/original.7dd03700e6417622b5fb895e4aadb5de01d668fd706513d0d93dc7980a5585dd.png)
Process for the manufacture of 1-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]- piperazine - US 9,133,144 B2 - PatentSwarm
![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
![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
![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
![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
![Piperazine‐ and DABCO‐bridged dinuclear N‐heterocyclic carbene palladium complexes: synthesis, structure and application to Hiyama coupling reaction - Wang - 2017 - Applied Organometallic Chemistry - Wiley Online Library Piperazine‐ and DABCO‐bridged dinuclear N‐heterocyclic carbene palladium complexes: synthesis, structure and application to Hiyama coupling reaction - Wang - 2017 - Applied Organometallic Chemistry - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/429ff11f-6e57-48d2-ac8a-e00b200aadd9/aoc3543-toc-0001-m.jpg)
Piperazine‐ and DABCO‐bridged dinuclear N‐heterocyclic carbene palladium complexes: synthesis, structure and application to Hiyama coupling reaction - Wang - 2017 - Applied Organometallic Chemistry - Wiley Online Library
![KR20140107357A - Process for the manufacture of 1-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]-piperazine - Google Patents KR20140107357A - Process for the manufacture of 1-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]-piperazine - Google Patents](https://patentimages.storage.googleapis.com/6d/7d/2b/150851a9b62c98/pct00014.png)