![Molecules | Free Full-Text | Design, Synthesis, In Vitro and In Silico Studies of New Thiazolylhydrazine-Piperazine Derivatives as Selective MAO-A Inhibitors Molecules | Free Full-Text | Design, Synthesis, In Vitro and In Silico Studies of New Thiazolylhydrazine-Piperazine Derivatives as Selective MAO-A Inhibitors](https://www.mdpi.com/molecules/molecules-25-04342/article_deploy/html/images/molecules-25-04342-g001.png)
Molecules | Free Full-Text | Design, Synthesis, In Vitro and In Silico Studies of New Thiazolylhydrazine-Piperazine Derivatives as Selective MAO-A Inhibitors
![Synthesis and Structure–Activity relationship of 1-(5-isoquinolinesulfonyl) piperazine analogues as inhibitors of Mycobacterium tuberculosis IMPDH - ScienceDirect Synthesis and Structure–Activity relationship of 1-(5-isoquinolinesulfonyl) piperazine analogues as inhibitors of Mycobacterium tuberculosis IMPDH - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0223523419303332-gr1.jpg)
Synthesis and Structure–Activity relationship of 1-(5-isoquinolinesulfonyl) piperazine analogues as inhibitors of Mycobacterium tuberculosis IMPDH - ScienceDirect
![Synthesis of Enantiomerically Pure 5-Substituted Piperazine-2-Acetic Acid Esters as Intermediates for Library Production | The Journal of Organic Chemistry Synthesis of Enantiomerically Pure 5-Substituted Piperazine-2-Acetic Acid Esters as Intermediates for Library Production | The Journal of Organic Chemistry](https://pubs.acs.org/cms/10.1021/acs.joc.9b00148/asset/images/medium/jo-2019-001489_0015.gif)
Synthesis of Enantiomerically Pure 5-Substituted Piperazine-2-Acetic Acid Esters as Intermediates for Library Production | The Journal of Organic Chemistry
Recent progress toward the asymmetric synthesis of carbon-substituted piperazine pharmacophores and oxidative related heterocycles - RSC Medicinal Chemistry (RSC Publishing)
![Science of Synthesis Knowledge Updates – Review on Piperazine Synthesis - Thieme Chemistry - Georg Thieme Verlag KG Science of Synthesis Knowledge Updates – Review on Piperazine Synthesis - Thieme Chemistry - Georg Thieme Verlag KG](https://www.thieme.de/statics/bilder/thieme/final/en/bilder/tw_chemistry/A_102ODC001_rdax_440x293.jpg)
Science of Synthesis Knowledge Updates – Review on Piperazine Synthesis - Thieme Chemistry - Georg Thieme Verlag KG
![Suggestion for N-substitution on the piperazine ring · Issue #8 · OpenSourceMycetoma/Series-1-Fenarimols · GitHub Suggestion for N-substitution on the piperazine ring · Issue #8 · OpenSourceMycetoma/Series-1-Fenarimols · GitHub](https://user-images.githubusercontent.com/36144572/37564799-410b84ce-2af1-11e8-8869-0b916576f0d5.png)
Suggestion for N-substitution on the piperazine ring · Issue #8 · OpenSourceMycetoma/Series-1-Fenarimols · GitHub
![Piperazine ring toxicity in three novel anti-breast cancer drugs: an in silico and in vitro metabolic bioactivation approach using olaparib as a case study | SpringerLink Piperazine ring toxicity in three novel anti-breast cancer drugs: an in silico and in vitro metabolic bioactivation approach using olaparib as a case study | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs00210-023-02413-9/MediaObjects/210_2023_2413_Figa_HTML.png)
Piperazine ring toxicity in three novel anti-breast cancer drugs: an in silico and in vitro metabolic bioactivation approach using olaparib as a case study | SpringerLink
![PDF] A modular lead-oriented synthesis of diverse piperazine, 1,4-diazepane and 1,5-diazocane scaffolds. | Semantic Scholar PDF] A modular lead-oriented synthesis of diverse piperazine, 1,4-diazepane and 1,5-diazocane scaffolds. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/32977da8e1e44b8ab45a1fdc6c40cdaf6823274a/2-Figure1-1.png)
PDF] A modular lead-oriented synthesis of diverse piperazine, 1,4-diazepane and 1,5-diazocane scaffolds. | Semantic Scholar
![DABCO bond cleavage for the synthesis of piperazine derivatives - RSC Advances (RSC Publishing) DOI:10.1039/C9RA07870C DABCO bond cleavage for the synthesis of piperazine derivatives - RSC Advances (RSC Publishing) DOI:10.1039/C9RA07870C](https://pubs.rsc.org/image/article/2019/RA/c9ra07870c/c9ra07870c-f1_hi-res.gif)
DABCO bond cleavage for the synthesis of piperazine derivatives - RSC Advances (RSC Publishing) DOI:10.1039/C9RA07870C
![Organics | Free Full-Text | Recent Advances in the Synthesis of Piperazines: Focus on C–H Functionalization Organics | Free Full-Text | Recent Advances in the Synthesis of Piperazines: Focus on C–H Functionalization](https://www.mdpi.com/organics/organics-02-00018/article_deploy/html/images/organics-02-00018-sch007.png)
Organics | Free Full-Text | Recent Advances in the Synthesis of Piperazines: Focus on C–H Functionalization
![Piperazine derivatives with central pharmacological activity used as therapeutic tools - Brito - 2019 - Fundamental & Clinical Pharmacology - Wiley Online Library Piperazine derivatives with central pharmacological activity used as therapeutic tools - Brito - 2019 - Fundamental & Clinical Pharmacology - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/7f7060b8-cc2a-498f-8487-06cb8c364f5c/fcp12408-fig-0001-m.jpg)
Piperazine derivatives with central pharmacological activity used as therapeutic tools - Brito - 2019 - Fundamental & Clinical Pharmacology - Wiley Online Library
![Piperazine ring formation by a single-module NRPS and cleavage by an α-KG-dependent nonheme iron dioxygenase in brasiliamide biosynthesis | SpringerLink Piperazine ring formation by a single-module NRPS and cleavage by an α-KG-dependent nonheme iron dioxygenase in brasiliamide biosynthesis | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs00253-020-10678-w/MediaObjects/253_2020_10678_Figa_HTML.png)
Piperazine ring formation by a single-module NRPS and cleavage by an α-KG-dependent nonheme iron dioxygenase in brasiliamide biosynthesis | SpringerLink
![Amazon | The 2016 World Market Forecasts for Imported Heterocyclic Compounds with Nitrogen Hetero-Atom(s) Only, Containing a Pyrimidine Ring, Piperazine Ring, or Unfused Triazine Ring, and Nucleic Acids and Salts | International, Amazon | The 2016 World Market Forecasts for Imported Heterocyclic Compounds with Nitrogen Hetero-Atom(s) Only, Containing a Pyrimidine Ring, Piperazine Ring, or Unfused Triazine Ring, and Nucleic Acids and Salts | International,](https://m.media-amazon.com/images/I/41cxA7LrU9L._AC_UF1000,1000_QL80_.jpg)