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Relevant bibliographies by topics / Piperidin

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Academic literature on the topic 'Piperidin'

Author: Grafiati

Published: 4 June 2021

Last updated: 27 July 2025

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Journal articles on the topic "Piperidin"

1

Šilhánková, Alexandra, Karel Šindelář, Karel Dobrovský, Ivan Krejčí, Jarmila Hodková, and Zdeněk Polívka. "Synthesis of New L-Proline Amides with Anticonvulsive Effect." Collection of Czechoslovak Chemical Communications 61, no. 7 (1996): 1085–92. http://dx.doi.org/10.1135/cccc19961085.

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Series of heterocyclic L-proline amides were prepared from BOC-L-proline and heterocyclic amines (mostly substituted piperazines and morpholines) via active ester with hydroxysuccinimide. 4-(4-Fluorobenzoyl)piperidine afforded L-proline 4-(4-(4-(4-fluorobenzoyl)piperidin-1-yl)benzoyl)piperidine (7b) simultaneously with expected L-proline 4-(4-fluorobenzoyl)piperidide (7a). D-Proline N-(3-(4-(3-chlorophenyl)piperazin-1-yl)propyl)amide (2) was prepared starting from D-proline. The amides were tested by methods of biochemical and behavioural pharmacology.

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Gelbrich, Thomas, Denise Rossi, and Ulrich J. Griesser. "Two polymorphs and the diethylammonium salt of the barbiturate eldoral." Acta Crystallographica Section C Crystal Structure Communications 68, no. 2 (2012): o65—o70. http://dx.doi.org/10.1107/s0108270111055120.

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Polymorph (Ia) of eldoral [5-ethyl-5-(piperidin-1-yl)barbituric acid or 5-ethyl-5-(piperidin-1-yl)-1,3-diazinane-2,4,6-trione], C11H17N3O3, displays a hydrogen-bonded layer structure parallel to (100). The piperidine N atom and the barbiturate carbonyl group in the 2-position are utilized in N—H...N and N—H...O=C hydrogen bonds, respectively. The structure of polymorph (Ib) contains pseudosymmetry elements. The two independent molecules of (Ib) are connectedviaN—H...O=C(4/6-position) and N—H...N(piperidine) hydrogen bonds to give a chain structure in the [100] direction. The hydrogen-bonded la

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3

Rádl, Stanislav, Wieland Hafner, Petr Hezký, Ivan Krejčí, Jan Proška, and Jan Taimr. "Molecular Modification of Anpirtoline, a Non-Opioid Centrally Acting Analgesic." Collection of Czechoslovak Chemical Communications 64, no. 2 (1999): 363–76. http://dx.doi.org/10.1135/cccc19990363.

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Molecular modification of anpirtoline (2a) is described. Several methods of preparation of 4-[(3-chlorophenyl)sulfanyl]-1-methylpiperidine (3a) and its demethylation led to the deazaanpirtoline (3c). Nucleophilic substitution of piperidine-4-thiole with 2-chloro-4-nitropyridine, 2,4-dichloro-6-methylpyridine, and 3,6-dichloropyridazine led to 2-chloro-4-(piperidin-4-ylsulfanyl)pyridine (6), 4-chloro-6-methyl-2-(piperidin-4-ylsulfanyl)pyridine (7), and 3-chloro-6-(piperidin-4-ylsulfanyl)pyridazine (8), respectively. 2-Chloro-6-(pyridin-4-ylsulfanyl)pyridine (10) and 4-[(2-chloropyridin-6-yl)sul

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Kalinowska-Tłuścik, Justyna, Agata Piaskowska, and Marcin Kołaczkowski. "Multifunctional arylsulfonamide derivatives with 5-HT6/5-HT7 receptor antagonistic activity: a structural study." Acta Crystallographica Section C Structural Chemistry 74, no. 11 (2018): 1477–86. http://dx.doi.org/10.1107/s2053229618013748.

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Nowadays, a search for antagonists co-acting on serotonin receptor subtypes 6 and 7 (5-HT6R and 5-HT7R, respectively) is of great interest due to the increasing number of patients suffering from dementia and related behavioural and psychological symptoms. The X-ray crystal structures of four promising multifunctional ligands in the hydrochloride forms were determined, namely 4-(6-fluoro-1,2-benzoxazol-3-yl)-1-[3-(3-methylbenzenesulfonamido)propyl]piperidin-1-ium chloride, C22H27FN3O3S+·Cl−, (I), 4-(6-fluoro-1,2-benzoxazol-3-yl)-1-[4-(5-fluoro-3-methylbenzo[b]thiophene-2-sulfonamido)butyl]piper

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Shafi, S. Syed, R. Rajesh, and S. Senthilkumar. "Synthesis and Biological Properties of New Piperidine Substituted Benzothiazole Derivatives." Asian Journal of Organic & Medicinal Chemistry 6, no. 3 (2021): 181–85. http://dx.doi.org/10.14233/ajomc.2021.ajomc-p333.

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In present work, ethyl 2-aminobenzo[d]thiazole-6-carboxylate was reacted to piperidine using copper(II) bromide to get ethyl 2-(piperidin-1-yl)benzo[d]thiazole-6-carboxylate. The reaction of ethyl 2-(piperidin- 1-yl)benzo[d]thiazole-6-carboxylate with NaOH produces 2-(piperidin-1-yl)benzo[d]thiazole-6- carboxylic acid. The inter-mediate 2-(piperidin-1-yl)benzo[d]thiazole-6-carboxylic acid have been isolated as stable compounds. The chemical structures of synthesized compounds were established based on the 1H & 13C NMR and IR spectral data. The mass of the novel compounds was established wi

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6

Penjisevic, Jelena, Vladimir Sukalovic, Deana Andric, et al. "Synthesis, biological evaluation and docking analysis of substituted piperidines and (2-methoxyphenyl)piperazines." Journal of the Serbian Chemical Society 81, no. 4 (2016): 347–56. http://dx.doi.org/10.2298/jsc151021097p.

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A series of sixteen novel substituted piperidines and (2-methoxyphenyl)piperazines were synthesized, starting from the key intermediates 1-(2-methoxyphenyl)-4-(piperidin-4-yl)piperazine and 1-(2-methoxyphenyl)-4-(piperidin-4-ylmethyl)piperazine. Biological evaluation of the synthesized compounds was pointed out for seven compounds, of which 1-(2-methoxyphenyl)-4-{[1-(2-nitrobenzyl)piperidin-4-yl]methyl}piperazine had the highest affinity for the dopamine D2 receptor. For all seven selected compounds docking analysis was performed in order to establish their structure-to-activity relationship.

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Chakkaravarthy, Jayaraman, Inbasekaran Muthuvel, and Ganesamoorthy Thirunarayanan. "Spectral investigations of some piperidin-4-one molecular addition compounds." Ovidius University Annals of Chemistry 31, no. 1 (2020): 18–26. http://dx.doi.org/10.2478/auoc-2020-0005.

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AbstractIn the present study, some 2- and 3-substituted piperidin-4-ones (A1-A3) were chosen as proton acceptor and maleic anhydride was chosen as proton donor. Piperidin-4-ones (A1, A2 ---amp--- A3) were mixed with maleic anhydride in ether medium and the corresponding molecular adduct products (B1, B2 ---amp--- B3) thus obtained were collected and purified. The 1H and 13C NMR spectra were recorded for piperidine-4-one and their addition compounds. The 1H and 13C NMR chemical shifts of products (B1, B2 ---amp--- B3) are analyzed and compared with those of the corresponding piperidine-4-ones (

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8

Romero, Nancy, Sylvain Bernès, Luis F. Roa, Joel L. Terán, and Dino Gnecco. "Crystal structures of two chiral piperidine derivatives: 1-[(1R)-2-hydroxy-1-phenylethyl]piperidin-4-one and 8-[(1S)-1-phenylethyl]-1,4-dioxa-8-azaspiro[4.5]decane-7-thione." Acta Crystallographica Section E Crystallographic Communications 71, no. 10 (2015): 1207–11. http://dx.doi.org/10.1107/s2056989015017119.

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The crystal structures of the two title piperidine derivatives show different conformations for the six-membered heterocycle. TheN-substituted 4-piperidinone 1-[(1R)-2-hydroxy-1-phenylethyl]piperidin-4-one, C13H17NO2, (I), has a chair conformation, while the piperidine substituted in position 2 with a thiocarbonyl group, 8-[(1S)-1-phenylethyl]-1,4-dioxa-8-azaspiro[4.5]decane-7-thione, C15H19NO2S, (II), features a half-chair conformation. Comparison of the two structures, and data retrieved from the literature, suggests that the conformational flexibility is mainly related to the hybridization

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9

Varenichenko, S. A., A. V. Kovtun, V. K. Farat, and O. K. Farat. "An efficient synthetic route to substituted xanthene analogues." Voprosy Khimii i Khimicheskoi Tekhnologii, no. 3 (June 2025): 100–106. https://doi.org/10.32434/0321-4095-2025-160-3-100-106.

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The reactions of N-[(9-chloro-1,2-dihydrocyclopenta[b]chromen-3-yl)methylene]-N-methylmethanaminium and N-[(11-chloro-7,8,9,10-tetrahydrocyclohepta[b]chromen-6-yl)methylene]-N-methylmethanaminium perchlorates with (1-phenylethylidene)malononitrile were studied in boiling acetonitrile in the presence of piperidine. These reactions led to the formation of new organic dyes, [(2E)-1-phenyl-3-(9-piperidin-1-yl-1,2-dihydrocyclopenta[b]chromen-3-yl)prop-2-en-1-ylidene]malononitrile and [(2E)-1-phenyl-3-(11-piperidin-1-yl-7,8,9,10-tetrahydrocyclohepta[b]chromen-6-yl)prop-2-en-1-ylidene]malononitrile,

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S, Harishkumar, Satyanarayan Nd, and Santhosha Sm. "ANTIPROLIFERATIVE AND IN SILICO ADMET STUDY OF NEW 4-(PIPERIDIN-1-YLMETHYL)-2- (THIOPHEN-2-YL) QUINOLINE ANALOGUES." Asian Journal of Pharmaceutical and Clinical Research 11, no. 4 (2018): 306. http://dx.doi.org/10.22159/ajpcr.2018.v11i4.24147.

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Objective: Synthesis and antiproliferative study of novel 4-(piperidin-1-ylmethyl)-2-(thiophen-2-yl) quinoline 7(a-j) derivatives.Methods: 4-(piperidin-1-ylmethyl)-2-(thiophen-2-yl) quinolines were synthesized by the addition of 4-(chloromethyl)-2-(thiophen-2-yl) quinoline (0.01 mol), piperidine (0.01 mol) in DMF (10 v) and K2CO3 (0.02 mol). The anticancer activity of the title compounds performed against T-47D, HeLa, HepG2, and MCF-7 human cancer cell lines growth was investigated by MTT assay.Results: The compounds 7b and 7g exhibited 90% of the growth inhibitory effect on T-47D, HeLa, and M

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Dissertations / Theses on the topic "Piperidin"

1

Stapper, Christian. "Ringumlagerungen und Synthese von Piperidin- und Pyrrolidinalkaloiden durch Olefinmetathese." [S.l.] : [s.n.], 2001. http://deposit.ddb.de/cgi-bin/dokserv?idn=962764485.

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NOGUE, DENISE. "Synthese regio et stereoselective d'heterocycles azotes via la reaction d'imino diels alder. Analyse conformationnelle de decahydroquinolein-4-ones et de piperidin-4-ones par correlation rmn #1h, m. M. Et rx." Paris 11, 1993. http://www.theses.fr/1993PA112254.

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Le travail rapporte dans ce memoire concerne d'une part la synthese d'heterocycles azotes tels que les n-aryl-2-aryl decahydroquinolein-4-ones et les n-aryl-2-aryl piperidin-4-ones et, d'autre part, leur analyse conformationnelle. L'etude de la reaction d'imino diels alder du 1-(1-trimethylsilyloxyethenyl)-cyclohexene et d'imines catalysee par des acides de lewis a permis d'obtenir selectivement ou tres majoritairement les enoxysilanes exo ou endo selon la nature des groupes aryles ar et ar lies respectivement au carbone et a l'azote de l'imine. Ainsi, l'utilisation du t-butyldimethylsilyle tr

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3

Lewis, Neil. "Asymmetric piperidine synthesis." Thesis, University of Nottingham, 1995. http://eprints.nottingham.ac.uk/13293/.

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It has been demonstrated that bakers' yeast reduction of 1-tert-butyl-2-methyl 3-oxo-piperidine-1,2-dicarboxylate gives (2R, 3S), 1-tert-butyl-2-methyl 3-hydroxy-piperidine-1,2-dicarboxylate in 80% chemical yield with >99% d.e. and >97% e.e. Also bakers' yeast reduction of 1-tert-butyl-3-ethyl 4-oxo-piperidine-1,3-dicarboxylate gives (3R, 4S), 1-tert-butyl-3-ethyl4-hydroxy-piperidine-1,3-dicarboxylate in 74% chemical yield with >99% d.e. and >93% e.e. The optical purity and absolute configurations of the hydroxy-ester derivatives were determined by conversion into the corresponding chiral bis-

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4

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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5

Rosset, Isac George. "Diazocetonas α,β-insaturadas como reagentes multifuncionais: aplicação na síntese de alcaloides piperidínicos e pirrolidínicos." Universidade de São Paulo, 2015. http://www.teses.usp.br/teses/disponiveis/75/75133/tde-20052015-101409/.

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p>O primeira parte do trabalho descreve a preparação de um novo reagente de olefinação de HWE para o preparo de diazocetonas α, β-insaturadas com geometria Z e aplicação na síntese de núcleos piperidínicos funcionalizados. Através da otimização da reação de HWE empregando o benzaldeído como aldeído padrão foi possível maximizar a obtenção do isômero Z desejado (92%, Z:E 9:1). As reações-chave para a formação dos núcleos piperidínicos foram a de olefinação de HWE utilizando amino-aldeídos, obtendo-se bons rendimentos e boa seletividade, seguida de uma reação de inserção N-H catalisad

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Ries, Stefan. "Versuche zur Totalsynthese von Pseudodistomin C und E - Ein neuer Syntheseweg." kostenfrei, 2009. http://www.opus-bayern.de/uni-wuerzburg/volltexte/2009/3993/.

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Geant, Pierre-Yves. "Synthèse d'aminoalcools assistée par un sulfoxyde chiral." Thesis, Montpellier 2, 2011. http://www.theses.fr/2011MON20169/document.

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Les travaux présentés dans ce mémoire décrivent une nouvelle voie de synthèse d'aminoalcools 1,2 à partir de γ-bromo-β-cétosulfoxydes, dans lesquels seul le centre stéréogène du soufre est défini. Cette synthèse s'appuie sur deux processus hautement stéréocontrôlés dirigés par le groupement sulfoxyde : le dédoublement cinétique dynamique lors de la substitution nucléophile du brome par la dibenzylamine et la réduction diastéréosélective du carbonyle. Les syn-γ-N,N-dibenzylamino-β-hydroxysulfoxydes correspondants ont été obtenus avec des excès diastéréoisomériques supérieurs à 95%. Les syn-γ-N,

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8

Taylor, Sarah Alison. "Sulfur-mediated pyrrolidine and piperidine synthesis." Thesis, University of Cambridge, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.613286.

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Turner, Ian. "Piperidines from tetrahydroimidazoles." Thesis, University of Nottingham, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.334848.

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10

Girling, Paul Ricardo. "Novel approaches to piperidine and hydropyridine derivatives." Thesis, Durham University, 2012. http://etheses.dur.ac.uk/6354/.

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Three new modes of reactivity are reported between the reaction of an imine, but-3-en-2-ones and a Lewis acid. These are formal [2+2+2]-, [1+2+1+2]- and [4+2]- cycloadditions, deriving 1,1'-(1,2-dihydropyridine-3,5-diyl)diethanones, 1,1'-(1,4-dihydropyridine-3,5-diyl)diethanones and piperidin-4-ones and respectively. The [2+2+2]- and [1+2+1+2]-cycloadditions proceed when R3 = LG (leaving group), with the [1+2+1+2]-pathway dominating when the imine is easily hydrolysed within the reaction conditions. When R3 ≠ LG, the cycloaddition proceeds through different [4+2]-mechanistic pathways, dependen

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Books on the topic "Piperidin"

1

Oetting, Jörg. Optisch aktive [beta]-Hydroxy-carbonsäuren [Beta-Hydroxy-carbonsäuren] als Bausteine für neue Amino-hydroxy-carbonsäuren und Piperidin-Alkaloide: Stereoselektive Totalsynthese von (-)-Cassin. [s.n.], 1995.

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Rubiralta, Mario. Piperidine: Structure, preparation, reactivity, and synthetic applications of piperidine and its derivatives. Elsevier, 1991.

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3

Williams, Jodi Thomas. Stereoselective piperidine synthesis via ene and carbonyl ene cyclisations. University of Birmingham, 2003.

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Hutchinson, Ian. The synthesis of 3-substituted-2-(nitromethylene)-piperidines. typescript, 1994.

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C, Heading R., and Wood Jack D, eds. Gastrointestinal dysmotility: Focus on cisapride. Raven Health Care Communications, 1992.

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6

Die Konstitutionserforschung der Alkaloide: Die Pyridin-Piperidin-Gruppe. In Kommission, Deutscher Apotheker Verlag, 1985.

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Stamenitis, Stamatios. Asymmetrische Synthesen [alpha]-quartärer Piperidin-2-carbonsäurederivate mit 1,4-Oxazin-2,5-dionen. 1994.

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8

Rubiralta, Mario. Piperidine. Elsevier, 1991.

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9

Meier, Galina. Histamin-H₃-Rezeptorliganden vom Nicht-Imidazoltyp: Synthese und pharmakologische Charakterisierung neuer Verbindungen abgeleitet von N-[3-(3-Phenylpropoxy)propyl]piperidin (FUB 637). 2004.

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Vardanyan, Ruben. Piperidine-Based Drug Discovery. Elsevier, 2017.

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Book chapters on the topic "Piperidin"

1

Hoffmann, G. F., C. D. Langhans, and A. Schulze. "Δ1-Piperidin-6-carbonsäure." In Lexikon der Medizinischen Laboratoriumsdiagnostik. Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-49054-9_2451-1.

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Hoffmann, G. F., C. D. Langhans, and A. Schulze. "Δ1-Piperidin-6-carbonsäure." In Springer Reference Medizin. Springer Berlin Heidelberg, 2019. http://dx.doi.org/10.1007/978-3-662-48986-4_2451.

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Wohlfarth, Ch. "Viscosity of the mixture (1) water; (2) 2-piperidin-2-ylethanol." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_510.

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Gooch, Jan W. "Piperidine." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_8770.

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Lide, David R. "Piperidine." In Handbook of Organic Solvents. CRC Press, 2024. http://dx.doi.org/10.1201/9781003575191-397.

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Howard, Philip H., Gloria W. Sage, William F. Jarvis, and D. Anthony Gray. "Piperidine." In Handbook of Environmental Fate and Exposure Data For Organic Chemicals, Volume II. CRC Press, 2023. http://dx.doi.org/10.1201/9781003418863-58.

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Khalid, Hira, Aziz-ur-Rehman, M. Athar Abbasi, et al. "Synthesis, Spectral Analysis and Biological Evaluation of 5-Substituted 1,3,4-Oxadiazole-2-yl-4-(Piperidin-1-ylsulfonyl)Benzyl Sulfide." In Emerging Trends in Chemical Sciences. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-60408-4_14.

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Schomburg, Dietmar, and Dörte Stephan. "Piperidine N-piperoyltransferase." In Enzyme Handbook 11. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-61030-1_275.

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Wohlfarth, Ch. "Viscosity of piperidine." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_159.

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Demaison, J. "573 C5H11N Piperidine." In Asymmetric Top Molecules. Part 2. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-10400-8_321.

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Conference papers on the topic "Piperidin"

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Raman, Aravamudhan. "Green Inhibitors for Coatings and Linings – Traditional vs. Green." In CORROSION 2004. NACE International, 2004. https://doi.org/10.5006/c2004-04410.

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Abstract Pigment additives containing chromates, red lead and excessive zinc, commonly used in olden times in paint systems, are toxic and barred from widespread usage. Use of Cr(III) salts instead of Cr(VI) in conversion coatings has been advocated. Methods have been tried to cover the toxic ingredients by non-toxic topcoats and to make them slow leaching by incorporating them in organometallic pigment form strongly bonded to the polymer base of the coating. Zinc phosphate and other zinc salts are being used instead of chromate salts and these are of the green type and offer excellent inhibit

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2

Symma, N., M. Bütergerds, J. Sendker, et al. "Neue Piperidin- und 3,4-dihydro-2H-pyrrol-Alkaloide aus Lindenblüten (Tiliae flos)." In Jubiläumskongress Phytotherapie 2021 Leib und Magen – Arzneipflanzen in der Gastroenterologie 50 Jahre Gesellschaft für Phytotherapie. Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/s-0041-1731511.

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Wang, Caolin, Yuanbiao Tu, Jiaqian Han, and Yuping Guo. "Synthesis of 1-(2-(piperidin-1-yl)ethyl)-1H-pyrrole-2-carbaldehyde." In 2016 7th International Conference on Education, Management, Computer and Medicine (EMCM 2016). Atlantis Press, 2017. http://dx.doi.org/10.2991/emcm-16.2017.114.

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Renk, D., M. Holschbach, D. Bier, and B. Neumaier. "Synthese von Aminobenzothiazolderivaten mit unterschiedlichen fluorhaltigen Piperidin- und Piperazin-Substituenten für die PET-Bildgebung des Adenosin-A 2A -Rezeptors." In NuklearMedizin 2020. © Georg Thieme Verlag KG, 2020. http://dx.doi.org/10.1055/s-0040-1708273.

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Craig, Norman, Alberto Lesarri, Emilio Cocinero, Patricia Ecija, Heinz Rudolph, and Jean Demaison. "EQUILIBRIUM STRUCTURE OF PIPERIDINE." In 69th International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2014. http://dx.doi.org/10.15278/isms.2014.wj12.

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Kovačková, Soňa, Martin Dračínský, and Dominik Rejman. "Piperidine nucleoside phosphonic acid derivatives." In XVth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2011. http://dx.doi.org/10.1135/css201112372.

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Malmakova, A., N. Kystaubayeva, T. Zharkinbek, M. Myrzakhanov, M. Balabekova та V. Yu. "Piperidine-containing phosphonates as immunоcorrectors". У 6TH INTERNATIONAL CONFERENCE ON ENVIRONMENT (ICENV2018): Empowering Environment and Sustainable Engineering Nexus Through Green Technology. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5117135.

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8

Okeke, Micheal, and Dong-Sheng Yang. "VIBRONIC SPECTRA OF GROUP 13 METAL-PIPERIDINE COMPLEXES." In 2021 International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2021. http://dx.doi.org/10.15278/isms.2021.tl10.

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9

Muliadi and Muhammad Nurdin. "Terbium piperidine dithiocarbamate with 2.2’ dimethyl-1.10 phenanthroline co-ligand." In 5TH INTERNATIONAL CONFERENCE ON ELECTRICAL, ELECTRONIC, COMMUNICATION AND CONTROL ENGINEERING (ICEECC 2021). AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0137981.

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Pereira, M. L. A., L. B. Sousa, T. R. Tomich, F. S. Machado, L. B. Sousa, and L. G. R. Pereira. "Methane mitigation potential of diets supplemented with mesquite piperidine alkaloids for sheep." In 6th EAAP International Symposium on Energy and Protein Metabolism and Nutrition. Wageningen Academic Publishers, 2019. http://dx.doi.org/10.3920/978-90-8686-891-9_22.

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Reports on the topic "Piperidin"

1

Banks, Harold D. Piperidine Synthesis. Defense Technical Information Center, 1992. http://dx.doi.org/10.21236/ada258925.

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2

Miranda, P. Mechanism of hydrodenitrogenation adsorption of piperidine on reduced molybdenum catalysts. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/7275171.

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3

Miranda, P. Mechanism of hydrodenitrogenation adsorption of piperidine on reduced molybdenum catalysts. Tenth quarterly report, January 1--March 31, 1992. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/10167178.

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