Relevant bibliographies by topics / Piperazine

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Piperazine'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 July 2025

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Journal articles on the topic "Piperazine"

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Kmoníček, Vojtěch, Martin Valchář, and Zdeněk Polívka. "Some 4-Substituted 1-(3-Pyridylmethyl)piperazines with Antihistamine Activity." Collection of Czechoslovak Chemical Communications 59, no. 10 (1994): 2343–50. http://dx.doi.org/10.1135/cccc19942343.

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Several compounds derived from nicotinic acid were prepared within a more extensive programme aiming at the synthesis of new substances with expected antihistamine and antidepressant activity. Some of these compounds display certain structural resemblance with the antidepressant agent piberaline (EGYT 475, Trelibet®, I) and its analogues. The products were used as intermediates for the synthesis of further compounds and most of them were subjected to pharmacological testing. Substituted nicotinic acid piperazides IIa - IId and IVa - IVe were obtained by reactions of nicotinoyl chloride (prepar
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Gettys, Kristen, Zhishi Ye, and Mingji Dai. "Recent Advances in Piperazine Synthesis." Synthesis 49, no. 12 (2017): 2589–604. http://dx.doi.org/10.1055/s-0036-1589491.

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Piperazine ranks as the third most common N-heterocycle appearing in small-molecule pharmaceuticals. This review highlights recent advances in methods development for the construction of the piperazine­ ring system with particular emphasis on preparing carbon-substituted piperazines.1 Introduction2 Reduction of (Di)ketopiperazine3 N-Alkylation4 Transition-Metal-Catalyzed/Mediated Piperazine Synthesis4.1 The SnAP and SLAP Methods4.2 Palladium-Catalyzed Cyclization4.3 Gold-Catalyzed Cyclization4.4 Other Metal-Catalyzed/Mediated Cyclization4.5 Borrowing Hydrogen Strategy4.6 Imine Reductive Cycliz
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Hafeez, Freeha, Ameer Fawad Zahoor, Azhar Rasul, et al. "Ultrasound-Assisted Synthesis and In Silico Modeling of Methanesulfonyl-Piperazine-Based Dithiocarbamates as Potential Anticancer, Thrombolytic, and Hemolytic Structural Motifs." Molecules 27, no. 15 (2022): 4776. http://dx.doi.org/10.3390/molecules27154776.

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Piperazine-based dithiocarbamates serve as important scaffolds for numerous pharmacologically active drugs. The current study investigates the design and synthesis of a series of dithiocarbamates with a piperazine unit as well as their biological activities. Under ultrasound conditions, the corresponding piperazine-1-carbodithioates 5a–5j were synthesized from monosubstituted piperazine 2 and N-phenylacetamides 4a–4j in the presence of sodium acetate and carbon disulfide in methanol. The structures of the newly synthesized piperazines were confirmed, and their anti-lung carcinoma effects were
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Durand, Carolina, and Michal Szostak. "Recent Advances in the Synthesis of Piperazines: Focus on C–H Functionalization." Organics 2, no. 4 (2021): 337–47. http://dx.doi.org/10.3390/org2040018.

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Piperazine ranks as the third most common nitrogen heterocycle in drug discovery, and it is the key component of several blockbuster drugs, such as Imatinib (also marketed as Gleevec) or Sildenafil, sold as Viagra. Despite its wide use in medicinal chemistry, the structural diversity of piperazines is limited, with about 80% of piperazine-containing drugs containing substituents only at the nitrogen positions. Recently, major advances have been made in the C–H functionalization of the carbon atoms of the piperazine ring. Herein, we present an overview of the recent synthetic methods to afford
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O’Malley, Karen, and Keith Vaughan. "Synthesis and Characterization of a Series of 1-Aryl-4-[Aryldiazenyl]-piperazines. Part II1. 1-Aryl-4-(2-Aryl-1-Diazenyl)-piperazines with Fluoro-, chloro-, Methyl-, Cyano- and Acetyl Substituents in The 1-Aryl Group." Open Chemistry Journal 3, no. 1 (2016): 42–55. http://dx.doi.org/10.2174/1874842201603010042.

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This paper reports the synthesis and characterization of eight series of 1-aryl-4-(2-aryl-1-diazenyl)-piperazines (12 to 19). Several series of these triazenes have been synthesized by the diazotization of a primary arylamine followed by diazonium coupling with a secondary arylpiperazine . The arylpiperazines used in this study are: 1-phenylpiperazine, 1-(4-fluorophenyl-)piperazine, 1-(4-chlorophenyl-)piperazine, 1-(3,4-dichlorophenyl-)piperazine, 1-(2-methylphenyl-)-piperazine, 1-(4-acetophenyl-)-piperazine, 1-(2-pyridyl-)piperazine and 2-cyanophenylpiperazine. These new triazenes (series 12-
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Kafka, Stanislav, Jan Čermák, Tomáš Novák, František Pudil, Ivan Víden, and Miloslav Ferles. "Syntheses of piperazines substituted on the nitrogen atoms with allyl, propyl, 2-hydroxypropyl and 3-hydroxypropyl groups." Collection of Czechoslovak Chemical Communications 50, no. 5 (1985): 1201–11. http://dx.doi.org/10.1135/cccc19851201.

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The paper describes synthesis of 1,4-diallylpiperazine (I), 1-allylpiperazine (III), 1-propylpiperazine (IV), 1-(1-piperazinyl)-2-propanol (V), 3-(1-piperazinyl)-1-propanol (VI), 1-allyl-4-propylpiperazine (VII), 1-(4-allyl-1-piperazinyl)-2-propanol (VIII), 3-(4-allyl-1-piperazinyl)-1-propanol (IX), 1,4-dipropylpiperazine (X), 1-(4-propyl-1-piperazinyl)-2-propanol (XI), 3-(4-propyl-1-piperazinyl)-1-propanol (XII), 1,4-bis(2-hydroxypropyl)piperazine (XIII), 3-[4-(2-hydroxypropyl)-1-piperazinyl]-1-propanol (XIV) and 1,4-bis(3-hydroxypropyl)piperazine (XV). Retention indices of I-XV reported and
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Little, Vanessa Renee, and Keith Vaughan. "Synthesis and characterization of several series of 4-acyl-1-[2-aryl-1-diazenyl]piperazines." Canadian Journal of Chemistry 92, no. 9 (2014): 838–48. http://dx.doi.org/10.1139/cjc-2014-0242.

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Five series of a novel class of 4-acyl-1-[2-aryl-1-diazenyl]piperazines have been synthesized and characterized: the 4-acetyl-1-[2-aryl-1-diazenyl]piperazines [series 1]; the 4-cyclohexylcarbonyl-1-[2-aryl-1-diazenyl]piperazines [series 2]; the 4-benzoyl-1-[2-aryl-1-diazenyl]piperazines [series 3]; the benzyl 4-[2-aryl-1-diazenyl]-1-piperazinecarboxylates [series 4]; and the t-butyl 4-[2-aryl-1-diazenyl]-1-piperazinecarboxylates [series 5]. The compounds were synthesized by diazotization of a primary aromatic amine and subsequent coupling to an appropriate secondary amine: 1-acetylpiperazine [
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Kiran Kumar, Haruvegowda, Hemmige S. Yathirajan, Belakavadi K. Sagar, Sabine Foro, and Christopher Glidewell. "Six 1-aroyl-4-(4-methoxyphenyl)piperazines: similar molecular structures but different patterns of supramolecular assembly." Acta Crystallographica Section E Crystallographic Communications 75, no. 8 (2019): 1253–60. http://dx.doi.org/10.1107/s2056989019010491.

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Six new 1-aroyl-4-(4-methoxyphenyl)piperazines have been prepared, using coupling reactions between benzoic acids and N-(4-methoxyphenyl)piperazine. There are no significant hydrogen bonds in the structure of 1-benzoyl-4-(4-methoxyphenyl)piperazine, C18H20N2O2, (I). The molecules of 1-(2-fluorobenzoyl)-4-(4-methoxyphenyl)piperazine, C18H19FN2O2, (II), are linked by two C—H...O hydrogen bonds to form chains of rings, which are linked into sheets by an aromatic π–π stacking interaction. 1-(2-Chlorobenzoyl)-4-(4-methoxyphenyl)piperazine, C18H19ClN2O2, (III), 1-(2-bromobenzoyl)-4-(4-methoxyphenyl)
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Nivedita Desai, R., S. Sreenivasa, S. Naveen, N. K. Lokanath, P. A. Suchetan, and D. B. Aruna Kumar. "Crystal structure of 2-(4-methylpiperazin-1-yl)quinoline-3-carbaldehyde." Acta Crystallographica Section E Crystallographic Communications 71, no. 11 (2015): o900—o901. http://dx.doi.org/10.1107/s2056989015020186.

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In the title compound, C15H17N3O, the aldehyde group is twisted relative to the quinoline group by17.6 (2)° due to the presence of a bulky piperazinyl group in theorthoposition. The piperazine N atom attached to the aromatic ring issp3-hybridized and the dihedral angle between the mean planes through the the six piperazine ring atoms and through the quinoline ring system is 40.59 (7)°. Both piperazine substituents are in equatorial positions.
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Jílek, Jiří, Martin Valchář, Jiří Holubek, et al. "Noncataleptic neuroleptic agents: 2-(4-(2-(2-Chloro-10,11-dihydrodibenzo[b,f]thiepin-10-yloxy)ethyl)piperazine-1-yl)ethanol and some related compounds." Collection of Czechoslovak Chemical Communications 53, no. 11 (1988): 2731–41. http://dx.doi.org/10.1135/cccc19882731.

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10-(2-Bromoethoxy)-2-chloro-10,11-dihydrodibenzo[b,f]thiepin (X), prepared by two methods, was subjected to substitution reactions with 2-(1-piperazinyl)ethanol, 3-(1-piperazinyl)propanol, 1-methylpiperazine, 3-(1-piperazinyl)propionamide, piperazine, and 1-(ethoxycarbonyl)piperazine and gave the title compounds II-VII. The alcohol II was esterified by treatment with acid chlorides to compounds VIII and IX. Compounds II, V, and VIII proved to be noncataleptic neuroleptic agents and II (clopithepin, VÚFB-17 076) was selected for preclinical studies.
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Dissertations / Theses on the topic "Piperazine"

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Moura, Rebeca Garcia. "Síntese de um fragmento precursor do Indinavir." Universidade de São Paulo, 2016. http://www.teses.usp.br/teses/disponiveis/46/46136/tde-11042017-075910/.

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Considerando-se a necessidade brasileira de se obterem fármacos a preços competitivos e usando tecnologia nacional, visamos sintetizar um fragmento do Indinavir empregando como material de partida a L-serina, um aminoácido natural de baixo custo. Desta maneira, desenvolvemos a seguinte rota, em 6 etapas: p-tosilação da serina, pelo uso de cloreto de p-tosila / NaOH; amidação da p-tosilserina, empregando-se o sal de terc-butilamônio da N-hidroxissuccinimida / DCC; ciclização da (S)-2-terc-butil-N-p-tosilserina, em condição de transferência de fase, com cloreto de p-tosila / carbonato de potássi
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Monaghan, S. M. "Synthetic studies in the piperazine-2,5-dione area." Thesis, Imperial College London, 1987. http://hdl.handle.net/10044/1/47304.

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Uddin, Farid. "Use of piperazine ligands for bleaching and epoxidation catalysis." Thesis, Queen Mary, University of London, 2011. http://qmro.qmul.ac.uk/xmlui/handle/123456789/692.

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Following reports that the dinuclear manganese complex of the ligand 1, 4, 7-trimethyl-1, 4, 7-triazacyclononane (TMTACN) was a potent bleaching catalyst, its catalytic oxidative activity was thoroughly studied. Apart from its catalytic bleaching activity, it has shown to be a versatile catalyst in terms of its substrate scope. In bleaching, it still remains the benchmark with regards to its catalytic bleaching activity against which systems in development are compared. Chapter one discusses the need for a bleaching catalyst in detergent formulations and the advantages it offers over existing
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Kuleya, Chipo. "The synthesis, analysis and characterisation of piperazine based drugs." Thesis, Anglia Ruskin University, 2014. https://arro.anglia.ac.uk/id/eprint/579889/1/Thesis%20%20final%20-%20Chipo%20Kuleya%20July%202015.pdf.

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This study developed a GC-MS method for the simultaneous detection of piperazines and congeners in street samples of amphetamine type stimulants. This research investigated the clandestine routes of synthesis and chemical profiles of phenylpiperazines, represented by 1- (4-fluorophenyl)piperazine (4-FPP) and 1-(3-trifluoromethylphenyl)piperazine (3-TFMPP). These drugs are part of the increasingly prevalent illicit new psychoactive substances. The presence of (2, 3, 4) FPP and (2, 3, 4) TFMPP positional isomers has been identified by other researchers as a limitation due to their similar
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Kuleya, Chipo. "The synthesis, analysis and characterisation of piperazine based drugs." Thesis, Anglia Ruskin University, 2014. http://arro.anglia.ac.uk/579889/.

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This study developed a GC-MS method for the simultaneous detection of piperazines and congeners in street samples of amphetamine type stimulants. This research investigated the clandestine routes of synthesis and chemical profiles of phenylpiperazines, represented by 1- (4-fluorophenyl)piperazine (4-FPP) and 1-(3-trifluoromethylphenyl)piperazine (3-TFMPP). These drugs are part of the increasingly prevalent illicit new psychoactive substances. The presence of (2, 3, 4) FPP and (2, 3, 4) TFMPP positional isomers has been identified by other researchers as a limitation due to their similar chemic
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Khan, Abdul Majeed 1980. "Síntese e termoquímica de adutos de brometos de metais bivalentes com aminas hetrocíclicas." [s.n.], 2013. http://repositorio.unicamp.br/jspui/handle/REPOSIP/249123.

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Orientador: Pedro Oliver Dunstan Lozano<br>Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Química<br>Made available in DSpace on 2018-08-22T07:28:40Z (GMT). No. of bitstreams: 1 Khan_AbdulMajeed_D.pdf: 3004508 bytes, checksum: 1d8c778094bf0cb1b93fa7bf80e19074 (MD5) Previous issue date: 2013<br>Resumo: Os adutos MX2.nL (M = Mn, Fe, Co, Ni, Cu ou Zn, L = 3-cianopiridina, piperidina ou piperazaina, X = Br, n = 0,5, 0,75, 1, 1,5, 2 ou 4), foram sintetizados e caracterizados através de análise elementar, determinação de pontos de fusão, espectroscopia IV e eletrônica e análise
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Bishnoi, Sanjay. "Carbon dioxide absorption and solution equilibrium in piperazine activated methyldiethanolamine /." Full text (PDF) from UMI/Dissertation Abstracts International, 2000. http://wwwlib.umi.com/cr/utexas/fullcit?p3004215.

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Safko, Jason P. "Luminescent Nitrogen and Sulfure Adducts of CuI Disubstituted Piperazine Complexes." W&M ScholarWorks, 2012. https://scholarworks.wm.edu/etd/1539626933.

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Tavet, Fabrice. "Nouveaux derives de la piperazine : synthese, relation structure-activite, proprietes pharmacologiques." Paris 5, 1991. http://www.theses.fr/1991PA05P617.

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Jakobsson, Josef. "Molecular mechanisms underlying platelet inhibition obtained by novel piperazine-purine analogues." Thesis, Örebro universitet, Institutionen för medicinska vetenskaper, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-93312.

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Introduction. MK-substances are a new class of piperazine-purine analogues bearing nitrate esters with confirmed cardioprotective, anti-inflammatory and antithrombotic effects. The length of the carbon side chain (spacer) connecting the nitrate ester to the basic molecular structure seems to be of importance for the platelet inhibitory effect but the molecular mechanisms underlying this are not yet fully understood. Aim. Establish molecular evidence explaining the observed differences in platelet inhibition obtained by a new group of piperazine-purine analogues with different spacer length. Me
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Books on the topic "Piperazine"

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Kagaku Busshitsu Hyōka Kenkyū Kikō and Shin Enerugī Sangyō Gijutsu Sōgō Kaihatsu Kikō (Japan), eds. Piperajin: Piperazine. Seihin Hyōka Gijutsu Kiban Kikō Kagaku Busshitsu Hyōka Kenkyū Kikō, 2007.

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Attorney-General, New Zealand. Report of the Attorney-General under the New Zealand Bill of Rights Act 1990 on the Misuse of Drugs (Classification of BZP) Amendment Bill 2007. House of Representatives, 2007.

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Great Britain. Health and Safety Executive. Occupational Medicine and Hygiene Laboratory. Organic isocyanates in air: Laboratory method using 1-(2-methoxyphenyl) piperazine solution and high performance liquid chromatography. HSE Books, 1994.

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Occupational Medicine and Hygiene Laboratory. Organic isocyanates in air: Laboratory method using 1-(2-methoxyphenyl) piperazine solution and high performance liquid chromatography. Health and Safety Executive, 1987.

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Sedefov, Roumen. Report on the risk assessment of BZP in the framework of the Council decision on new psychoactive substances. Office for Official Publications of the European Communities, 2009.

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1935-, Gingell Clive, ed. Management of ED: Focus on sildenafil : a urologist's approach. PharmaLibri, 1998.

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J, Fowler Clare, ed. Management of ED: Focus on sildenafil : a neurologist's approach. PharmaLibri, 1999.

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Botz-Bornstein, Thorsten. The philosophy of Viagra: Bioethical responses to the viagrification of the modern world. Rodopi, 2011.

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Bain, Joseph Paul 1914. Derivatives of Piperazine VIII: Synthesis of Substituted Piperazines and Reactions of Piperazines with Conjugated Systems. Creative Media Partners, LLC, 2021.

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Derivatives of Piperazine IV . . Creative Media Partners, LLC, 2021.

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Book chapters on the topic "Piperazine"

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de Groot, Anton C. "Piperazine." In Monographs In Contact Allergy. CRC Press, 2022. http://dx.doi.org/10.1201/9781003158004-391.

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Hirota, E., K. Kuchitsu, T. Steimle, J. Vogt, and N. Vogt. "116 C4H10N2 Piperazine." In Molecules Containing Three or Four Carbon Atoms and Molecules Containing Five or More Carbon Atoms. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-41504-3_117.

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Alicante, Raquel. "Piperazine Azopolymer Thin Films." In Springer Theses. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-31756-9_4.

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Laux, Gerd. "Piperazine Phenothiazines: Fluphenazine and Perphenazine." In NeuroPsychopharmacotherapy. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-62059-2_474.

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Eller, Sarah, and Marcelo Dutra Arbo. "Piperazine Designer Drugs of Abuse." In Handbook of Substance Misuse and Addictions. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-92392-1_166.

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Laux, Gerd. "Piperazine Phenothiazines: Fluphenazine and Perphenazine." In NeuroPsychopharmacotherapy. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-319-56015-1_474-1.

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Eller, Sarah, and Marcelo Dutra Arbo. "Piperazine Designer Drugs of Abuse." In Handbook of Substance Misuse and Addictions. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-67928-6_166-1.

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Bährle-Rapp, Marina. "Diethylene Glycolamine/Epichlorohydrin/Piperazine Copolymer." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_2932.

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Winkelmann, Jochen. "Diffusion coefficient of piperazine in water." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_335.

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Wills, Brandon, and Timothy Erickson. "Psychoactive Phenethylamine, Piperazine, and Pyrrolidinophenone Derivatives." In Medical Toxicology of Drug Abuse. John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118105955.ch10.

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Conference papers on the topic "Piperazine"

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Akkor, Ilayda, Shachit S. Iyer, John Dowdle, Le Wang, and Chrysanthos Gounaris. "Economic Optimization and Impact of Utility Costs on the Optimal Design of Piperazine-Based Carbon Capture." In Foundations of Computer-Aided Process Design. PSE Press, 2024. http://dx.doi.org/10.69997/sct.147100.

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Recent advances in process design for solvent-based, post-combustion capture (PCC) processes, such as the Piperazine/Advanced Flash Stripper (PZ/AFS) process, have led to a reduction in the energy required for capture. Even though PCC processes are progressively improving in Technology Readiness Levels (TRL), with a few commercial installations, incorporating carbon capture adds cost to any operation. Hence, cost reduction will be instrumental for proliferation. The aim of this work is to improve process economics through optimization and to identify the parameters in our economic model that h
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Huang, Shengyuan, Olajide Otitoju, Yao Zhang, and Meihong Wang. "Technical Assessment of direct air capture using piperazine in an advanced solvent-based absorption process." In The 35th European Symposium on Computer Aided Process Engineering. PSE Press, 2025. https://doi.org/10.69997/sct.124483.

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Climate and environmental problems caused by increasing CO2 concentration in the atmosphere make the direct air capture (DAC) technology having great prospects for development. As the widely used solvent in carbon capture based on chemical absorption processes, MEA still fails to address the issues of high energy consumption and high costs when used in DAC process. In this study, piperazine (PZ) was used as the new solvent for DAC process. The new configuration was simulated in Aspen Plus� V11 and the model was validated through experimental data and model comparison. It is followed by investi
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Peng, Lei, Qiang Fu, Zhi Li, Musong Lin, Yaohong Zhao, and Zaikun Wu. "Investigate of mass transfer of CO2 absorption into the mixed solution of piperazine and diethanolamine in a packed column." In Fifth International Conference on Green Energy, Environment, and Sustainable Development, edited by Mohammadreza Aghaei, Hongyu Ren, and Xiaoshuan Zhang. SPIE, 2024. http://dx.doi.org/10.1117/12.3044925.

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Pazdera, P., B. Andělová, and D. Němečková. "Utilization of piperazine for interphase catalytic systems." In The 13th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00192.

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Loupias, Pauline, Alexandra Dassonville-Klimpt, Elodie Lohou, Nicolas Taudon, and Pascal Sonnet. "Trojan horse strategy: synthesis of piperazine-based siderophores." In 4th International Electronic Conference on Medicinal Chemistry. MDPI, 2018. http://dx.doi.org/10.3390/ecmc-4-05579.

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Zhang, Xiaoguang, Xuexing Chen, Qingchun Chen, et al. "Preparation and Co (II) Removal of ZnO/Poly-Piperazineamide Nanofiltration Membranes." In 2017 25th International Conference on Nuclear Engineering. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/icone25-67740.

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A series of nanofiltration membranes were prepared by interfacial polymerization of piperazine and terephthaloyl chloride on the surface of polyacrylonitrile (PAN) ultrafiltration membranes. ZnO nanoparticles were incorporated in the active separation layer to modify the performances of the membranes. The preparation conditions as the monomer concentration, dosage of nano-ZnO particles and the reaction time on removal of a simulated radioactive nuclide Co (II) were investigated. Fourier transform infrared in attenuated total reflection mode verified the formation of polyamide on the PAN ultraf
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Lee, Young Bok, Gina Chun, Deog J. Kim, et al. "Abstract 1371: Antitumor activity of a new quinoxalinyl-piperazine compound." In Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-1371.

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Huff, D. W., and P. Murphy. "350. Piperazine: Development and Validation of an Air Monitoring Method." In AIHce 1998. AIHA, 1999. http://dx.doi.org/10.3320/1.2762752.

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Chen, Guan-He, Meng-Hui Li, and Rhoda B. Leron. "Henry’s Law Constant of CO2 in Aqueous Blends of Diethylenetriamine + Piperazine." In Annual International Conference on Chemistry, Chemical Engineering and Chemical Process. Global Science & Technology Forum (GSTF), 2015. http://dx.doi.org/10.5176/2301-3761_ccecp15.30.

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Meyer, P., and B. Czarnecki. "398. 1-(2-Pyridyl) Piperazine Stability on Coated Glass Fiber Filters." In AIHce 1996 - Health Care Industries Papers. AIHA, 1999. http://dx.doi.org/10.3320/1.2765077.

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Reports on the topic "Piperazine"

1

Rochelle, Gary, Fred Closmann, Jorge Martorell, et al. Front-End Engineering Design for Piperazine with the Advanced Stripper. Office of Scientific and Technical Information (OSTI), 2022. http://dx.doi.org/10.2172/1878608.

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John T. Cullinane. THERMODYNAMICS AND KINETICS OF AQUEOUS PIPERAZINE WITH POTASSIUM CARBONATE FOR CARBON DIOXIDE ABSORPTION. Office of Scientific and Technical Information (OSTI), 2005. http://dx.doi.org/10.2172/839556.

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Marcus Hilliard. THERMODYNAMICS OF AQUEOUS PIPERAZINE/POTASSIUM CARBONATE/CARBON DIOXIDE CHARACTERIZED BY THE ELECTROLYTE NRTL MODEL WITHIN ASPEN PLUS. Office of Scientific and Technical Information (OSTI), 2005. http://dx.doi.org/10.2172/838130.

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4

Chen, Eric, Steven Fulk, Matt Beaudry, et al. Evaluation of Concentrated Piperazine for CO2 Capture from Coal-Fired Flue Gas (Final Report, REV0). Office of Scientific and Technical Information (OSTI), 2019. http://dx.doi.org/10.2172/1512446.

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