Relevant bibliographies by topics / Pyrido[1

Contents

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

Academic literature on the topic 'Pyrido[1'

Author: Grafiati
Published: 4 June 2021
Last updated: 26 July 2025

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Journal articles on the topic "Pyrido[1"

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Cablewski, Teresa, Erin J. Carter, Craig L. Francis, Andris J. Liepa, and Michael V. Perkins. "N,N-Dialkyl-N′-Chlorosulfonyl Chloroformamidines in Heterocyclic Synthesis. III. Pyrido- and Pyridazo-Fused [1,2,4,6]Thiatriazine Dioxides." Australian Journal of Chemistry 60, no. 2 (2007): 105. http://dx.doi.org/10.1071/ch06367.

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N,N-Dialkyl-N′-chlorosulfonylchloroformamidines 1 reacted with 2-aminopyridines 2 to give novel pyrido[1,2-b][1,2,4,6]thiatriazine dioxides 3 and pyrido[2,1-c][1,2,4,6]thiatriazine dioxides 4. Reaction of 1 with 3-aminopyridazines 5 afforded pyridazo[3,2-c][1,2,4,6]thiatriazine dioxides 6 and a pyridazo[2,3-b][1,2,4,6]thiatriazine dioxide 7. The compounds 6 and 7 are derivatives of new ring systems.
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Refat, Hala M., and Khaled S. Mohamed. "Efficient and convenient synthesis of pyrido [2,1-b]benzothiazole, pyrimidopyrido[2,1-b]benzothiazole and benzothiazolo[3,2-a][1,8]naphthyridine derivatives." Heterocyclic Communications 21, no. 4 (2015): 219–24. http://dx.doi.org/10.1515/hc-2015-0018.

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AbstractNew 3-aryl-pyrido[2,1-b][1,3]benzothiazole derivatives 2a–e were synthesized in excellent yields via the reaction of benzothiazoleacetonitrile (1) with different aromatic aldehydes. The treatment of 2-(benzo[d]thiazol-2-yl)-3-(pyridin-4-yl)acrylonitrile (6) with malononitrile afforded 1-amino-3-(pyridin-4-yl)-3H-pyrido[2,1-b][1,3]benzothiazole-2,4-dicarbonitrile (7), which was allowed to react with a variety of reagents to provide pyrimido[5′,4′:5,6]pyrido[2,1-b][1,3]benzothiazole 8, 9 and [1,3]benzothiazolo[3,2-a][1,8]naphthyridine 10, 15 derivatives. All synthesized products were con
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Khan, Muhammad Naeem, Misbahul Ain Khan, Noreen Aslam, Pir Bakhsh Khan, and Ehsan ul Haq. "Tetracyclic Heteroaromatic Systems-Synthesis of Ethoxycarbonylphenylpyrido[3',2':5,6] Thiopyranoquinolines." Pakistan Journal of Scientific & Industrial Research Series A: Physical Sciences 64, no. 3 (2021): 191–94. http://dx.doi.org/10.52763/pjsir.phys.sci.64.3.2021.191.194.

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7-benzylideneamino-5H-thiochromeno[2,3-b]pyridin-5-ones and 9-benzylideneamino-5H-thio- chromeno[2,3-b]pyridin-5-ones, on reaction with ethyl pyruvate to afford 1-ethoxycarbonyl-3-phenyl-12H- pyrido[3',2':5,6]thiopyrano[3,2-f]quinoline-12-ones and 4-ethoxycarbonyl-2-phenyl-7H- pyrido[3',2':5,6]thiopyrano[3,2-h]quinoline-7-ones respectively by the two different methods. These products were precipitated by addition of ethanol, water (1:1), were purified by recrystalizing from appropriate solvents and were characterized from their IR, 1H-NMR, mass spectra and elemental analysis data.
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Yegorova, Tatyana, Bogdan Barnych, and Zoia Voitenko. "Reaction of pyrido[2,1-a]isoindole with 1,4-naphtoquinone and study of the product by spectroscopic methods." French-Ukrainian Journal of Chemistry 4, no. 2 (2016): 33–39. http://dx.doi.org/10.17721/fujcv4i2p33-39.

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Key role of the electronic structure of condensed isoindols in the way of the rearrangement was shown. Influence of the dienophile manifests in the requirement of the cyclic form of the dienophile itself. In the reaction of pyrido[2,1-a]isoindole with naphtoquinone rearrangement product of the first type was obtained and its structure was proven by spectral methods. Spectral criteria for the rearranged adducts of the first type for the pyrido[2,1-a]isoindole in the 13C NMR spectra were established. Products of reactions with naphthoquinone, 4-fluoro-, 2,5-difluorophenylmaleimides were isolated
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Tomashenko, Olesya A., Alexander F. Khlebnikov, Ivan P. Mosiagin, et al. "A new heterocyclic skeleton with highly tunable absorption/emission wavelength via H-bonding." RSC Advances 5, no. 115 (2015): 94551–61. http://dx.doi.org/10.1039/c5ra17755c.

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A new heterocyclic system, pyrido[2,1-a]pyrrolo[3,2-c]isoquinoline, showing stimuli responsive fluorescence, was synthesized via Pd-catalyzed intramolecular cyclization of 1-[1-benzyl-2-(2-bromophenyl)-1H-pyrrol-3-yl]pyridin-1-ium bromides.
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Abhishek, S. Saxena, Goel Atul, and Ji Ram Vishnu. "A convenient and expwitious synthesis of annulated N, S-heterocycles." Journal of Indian Chemical Society Vol. 80, Apr 2003 (2003): 311–18. https://doi.org/10.5281/zenodo.5839578.

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Medicinal Chemistry Division, Central Drug Research ln$titute, Lucknow-226 001, India E-mail : vjiram@yahoo.com_ Fax: 91-522-223405 <em>Manuscript received 19 September 2002</em> A convenient synthesis of titiett[2,3-<em>b</em>]pyridines (3), thieno[3,2-<em>c</em>]pxridines (4), pyrazolo[3,4-<em>b</em>]ipyridines (6), thieno[2,3- <em>d</em>]pyrimidines (9), pyridoll,2-althienol2,3-dlpyrimidines (11), pyrido[1,2-<em>a</em>]pyrimido141,51 : 4,5[thien:o[2,3-<em>d</em>]pyrimidines (12), pyrido[1,2-<em>a</em>]pyrimido[4,5-<em>d</em>]pyiimidines (13) and pyrazolor[3,4-<em>d</em>]pyrimido[1,2-a]pyrim
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Li, Ting, Zhen Wang, Mingliang Zhang, Hui-Jun Zhang та Ting-Bin Wen. "Rh/Cu-catalyzed multiple C–H, C–C, and C–N bond cleavage: facile synthesis of pyrido[2,1-a]indoles from 1-(pyridin-2-yl)-1H-indoles and γ-substituted propargyl alcohols". Chemical Communications 51, № 31 (2015): 6777–80. http://dx.doi.org/10.1039/c5cc01412c.

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The Rh/Cu-catalyzed synthesis of pyrido[2,1-a]indoles from 1-(pyridin-2-yl)-1H-indoles and γ-substituted propargyl alcohols involving multiple C–H, C–C, and C–N bond cleavage and construction is presented.
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Ma, Xingling, Lei Liu, Na Cao, Qiaogen Zou, Kaihe Xiong, and Pingkai Ouyang. "Isolation and Structural Elucidation of Palbociclib’s Eight Process-Related Impurities: Two Identified as New Compounds." Journal of AOAC INTERNATIONAL 99, no. 3 (2016): 638–48. http://dx.doi.org/10.5740/jaoacint.15-0251.

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Abstract Palbociclib is the first U.S. Food and Drug Administration-approved cyclin-dependent kinase inhibitor indicated in combination with letrozole for the treatment of breast cancer. Development of a selective method for the determination of any impurities contained in this drug is significantly important to ensure the quality and safety of palbociclib. In this study, a reliable reversed-phase HPLC method for the separation and determination of eight potential impurities was developed and validated. The structures of two new compounds and six other process-related impurities were character
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Tank, Manishkumar Jinabhai, Navinkumar A. Kucha, Chirag G. Naik, Tina R. Barot, and G. M. Malik. "Adamantane-pyrido[2,3-d]pyrimidine Derivatives; Synthesis, Characterization and Investigation of Antimicrobial Study." Oriental Journal Of Chemistry 39, no. 2 (2023): 393–402. http://dx.doi.org/10.13005/ojc/390219.

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Target molecules based on Adamantane-pyrido[2,3-d]pyrimidine derivatives were prepared. Adamantane-pyrido[2,3-d]pyrimidine series using N-(hydroxyadamantan-1-yl)-5-(2,4-substitutedphenyl)-2-Methyl-4-Oxo-7-(2-oxo-2H-Chromen-3-yl)pyrido[2,3-d]Pyrimidine-3(4H)carboxamide (6a-j) was synthesized by reaction between 3-(2-chloroacetyl)-5-(2,4-substitutedphenyl)-2-Methyl-7-(2-Oxo-2H-Chromen-3-yl) pyrido[2,3-d]pyrimidin-4(3H)-one (5a-j) and 3-aminoadamantan-1-ol. These derivatives of Adamantane-pyrido[2,3-d]Pyrimidine were investigated in vitro for their biological characteristics against the strains w
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Mohareb, R. M., and S. M. Fahmy. "Cyanothioacetamide in Heterocyclic Synthesis: A New Approach for the Synthesis of 2-Pyridothione and 2-Pyridazinothione Derivatives." Zeitschrift für Naturforschung B 41, no. 1 (1986): 105–9. http://dx.doi.org/10.1515/znb-1986-0122.

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Abstract Cyanothioacetamide (1) undergoes self condensation to give 4,6-diamino-3-cyano-2-pyrido-thione (2). The latter was utilised in synthesis of pyrido[2,3-c]pyrazole, pyrido[2,3-d]pyrim idine, bis-(pyridothione derivatives) through reaction with hydrazine hydrate, ethoxycarbonyl isothio-cyanate and cinnamonitrile derivatives. Also 1 undergoes self dimerisation to give 13, the latter form the pyridazine derivative on coupling with benzenediazonium chloride.
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Dissertations / Theses on the topic "Pyrido[1"

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Meyer, Holger. "Pyrido[3,2-b]indol-4-yl-amine, [1]Benzofuro[3,2-b]pyridin-4-yl-amine und [1]Benzothieno[3,2-b]pyridin-4-yl-amine : Darstellung von Antimalariamitteln /." [S.l. : s.n.], 2003. http://www.gbv.de/dms/bs/toc/374105367.pdf.

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Lancelot, Jean-Charles. "Synthèse et étude physicochimique des pyrido (3,2-e) pyrrolo (1,2-a) pyrazines, pyrido (2,3-e) pyrrolo (1,2-a) pyrazines, pyrazino (2,3-e) pyrrolo (1,2-a) pyrazines, (pyrrolyl-1)-8 triazolo-1, 2, 4 (4,3-a) pyridines, 6H-pyrido (2,3-c) pyrrolo (1,2-e) triazépines-1,2,5, pyrido (2,3-h) pyrrolo (1,2-a) quinoxalines." Caen, 1989. http://www.theses.fr/1989CAEN4023.

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Wilpert, Carsten. "Pyrido[3,2-e][1,4]diazepine : Synthese und Prüfung auf Anti-HIV-1-Wirkung /." [S.l. : s.n.], 1995. http://www.gbv.de/dms/bs/toc/184661447.pdf.

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Fernandez, Beatriz. "New functionalisation chemistry of 2- and 4-pyridones and related heterocycles." Thesis, Loughborough University, 2016. https://dspace.lboro.ac.uk/2134/21685.

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New methodology for the synthesis of several 4H-pyrido[1,2-a]pyrimidin-4-ones has been developed from commercially available 2-aminopyridines and β-oxo esters catalysed by Montmorillonite under solvent-free conditions in good yields. This methodology was expanded for the synthesis of 4H-pyrimido[1,2-a]pyrimidin-4-one derivatives from 2-aminopyrimidine and different β-keto esters. The new methodology for the synthesis of N-alkylated 6-methyl 2-pyridones and N-alkylated 2-methyl 4-pyridones, from commercially available starting materials was developed. For the synthesis of N-alkylated 6-methyl 2
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Belaroussi, Rabia. "Synthèse et fonctionnalisation de nouveaux dérivés tricycliques [6-5-6] polyhétéroaromatiques à visée thérapeutique potentielle." Thesis, Orléans, 2016. http://www.theses.fr/2016ORLE2002/document.

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La découverte de nouveaux candidats susceptibles de lutter contre différentes pathologies, en l’occurrence le cancer et les maladies neurodégénératives, constitue l’un des principaux objectifs de notre groupe de recherche. Dans ce contexte, les travaux de cette thèse ont pour but principal, la conception de deux nouvelles classes d’hétérocycles de structure planes, jusqu’à ce jour, très rarement étudiées, à savoir les pyrido[2’,1’ :1,5]pyrazolo[3,4-d]pyridazines et les pyrido[2’,1’ :1,5]pyrazolo[3,4-d]pyrimidines. Ce manuscrit est essentiellement dédié à un travail de méthodologie décrivant le
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Modolo, Isabelle. "Studies toward completion of the C1-C28 segment of spongistatin 1. Synthesis and photochemistry of 4bH-pyrido[2,1-a]isoindol-6-one." The Ohio State University, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=osu1236277748.

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Griffon, Du Bellay Amaury. "Synthèse de ligands du récepteu de l'Urotensine II et des récepteurs de la Mélatonine. Composés à noyau pyrido[2,3-d]pyrimidine ou imidazo[1,2-a]pyridine." Phd thesis, Université d'Orléans, 2008. http://tel.archives-ouvertes.fr/tel-00418219.

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L'Urotensine II est un peptide vasoactif que l'on retrouve chez toutes les espèces étudiées. Elle présente une partie N-terminale linéaire variable selon l'espèce et une partie C-terminale hexocyclique constante et responsable de l'activité. Parmi les ligands développés, le Palosuran, un inhibiteur sélectif du récepteur de l'Urotensine II, présente un intérêt dans le traitement de l'insuffisance rénale du patient diabétique voire dans certaines pathologies ischémiques. Dans la première partie de ce travail de thèse, une série de composés à noyau pyrido[2,3-d]pyrimidine a été développée, tout d
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Ejjoummany, Abdelaziz. "Design et fonctionnalisation d’hétérocycles originaux de type bicycliques [5-5] et tricycliques [6-5-6] à visée thérapeutique potentielle." Thesis, Orléans, 2020. http://www.theses.fr/2020ORLE3141.

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L’accès à de nouveaux composés hétérocycliques originaux biologiquement actifs, constitue l’un des principaux objectifs de notre groupe de recherche. Dans ce contexte, les travaux de cette thèse ont pour but principal, la conception de trois nouvelles familles de composés hétérocycliques contenant un motif pyrazolique susceptibles de présenter des activités biologiques, à savoir les pyrido[1',2':1,5]pyrazolo[4,3-d]pyrimidine, les pyrrolo[3,4-c]pyrazoles et les pyrazolo[5,1-b]thiazoles. Ce manuscrit est essentiellement dédié à un travail de méthodologie décrivant les différentes voies d’accès à
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Kaminski, Thomas. "Synthèse de dérivés de la 4-(méthylnitroasamino)-1-(3-pyridyl)-1-butanone (NNK)." Thesis, Metz, 2007. http://www.theses.fr/2007METZ046S/document.

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La synthèse de dérivés de 4-(méthylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) que nous décrivons se divise en deux parties. La première consiste en la synthèse de dérivés de NNK portant une chaîne alkyl oméga-fonctionnalisée sur la fonction nitrosamine. Pour cela, nous avons synthétisé la 3-[2-(3-pyridinyl)-1,3-dioxolan-2-yl]propylamine, intermédiaire clef dans notre synthèse, et qui nous offre de nombreuses possibilités quant à la fonctionnalisation de l'amine terminale. La seconde partie consiste à fonctionnaliser le cycle pyridinique de la NNK. Nous avons imaginé différentes méthodes de sy
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Kaminski, Thomas Kirsch Gilbert. "Synthèse de dérivés de la 4-(méthylnitroasamino)-1-(3-pyridyl)-1-butanone (NNK)." [S.l.] : [s.n.], 2007. ftp://ftp.scd.univ-metz.fr/pub/Theses/2007/Kaminski.Thomas.SMZ0746.pdf.

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Books on the topic "Pyrido[1"

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Hamburg, Universität, ed. Antitumoraktive Pyrido[3,2-d]-1-benzazepine. [s.n.], 1996.

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Friesenegger, Susanne. Metabolismus von 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanon (NNK) in Gewebeschnitten von Syrischen Goldhamstern. [s.n.], 1999.

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Braunschweig, Technische Universität, ed. Pyrido<3,2-b>indole, <1>Benzofuro<3,2-b>pyridine und <1>Benzothieno<3,2-b>pyridine. 1991.

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Malone, Almut. First-Pass-Metabolismus von 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanon, NNK, am Dünndarm der Ratte. 1991.

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Diel, Jens Michael. Untersuchungen zur Wirkung von Bis(1-(4-methylpiperidino)-4-(2-pyridyl)- 2,3-diazapenta-1,3-dien-1-thiolato-N',N3,S) nitrato-bismuth(III)), KP 1194 auf das klonogene Wachstum explantierter Tumorzellen in vitro. 1998.

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Decker-Burgard, Sabine. Antimutagene Effekte verschiedener Apfeisorten, Orangen- und Grapefruitchargen im Salmonella/Reversions-Test gegenüber den Mutagenen 2-Amino-3-methylimidazo (4, 5-f)chinolin (IQ), 2-Amino-1-methyl-6-phenylimidazo (4, 5-b)pyridin (PhIP), Benzo(a)pyren, 2-Nitrofluoren, 2,4,7-Trinitro-9-fluorenon, Natriumazid, [beta]-Propiolacton und Captafol. 1995.

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Book chapters on the topic "Pyrido[1"

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Negishi, Tomoe, Sakae Arimoto, Chiharu Nishizaki, and Hikoya Hayatsu. "Inhibition of the Genotoxicity of 3-Amino-1-Methyl-5H- Pyrido[4,3-b]Indole (Trp-P-2) in Drosophila by Chlorophyll." In Antimutagenesis and Anticarcinogenesis Mechanisms II. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4615-9561-8_29.

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Negishi, Tomoe, Hiromi Nakano, Sakae Arimoto, Haruki Rai, and Hikoya Hayatsu. "Inhibitory Activity of Natural Chlorophylls on the Mutagenicity of 4-Nitroquinoline 1-Oxide and 3-Amino-1-Methyl-5H-Pyrido[4,3-b]indole in Drosophila." In Food Factors for Cancer Prevention. Springer Japan, 1997. http://dx.doi.org/10.1007/978-4-431-67017-9_115.

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Shiotani, Bunsyo, Hitoshi Ashida, Yuji Nonaka, Takashi Hashimoto, Kazuki Kanazawa, and Gen-ichi Danno. "A Tryptophan Pyrolysis Product, 3-Amino-1,4-dimethyl-5H-pyrido[4,3-b]indole (Trp-P-1) but Not Its Metabolite Induces Apoptosis in Primary Cultured Rat Hepatocytes." In ACS Symposium Series. American Chemical Society, 2003. http://dx.doi.org/10.1021/bk-2003-0851.ch013.

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Morgan, Michael M., MacDonald J. Christie, Thomas Steckler, et al. "(–)-1-Methyl-2-(3-Pyridyl)Pyrrolidine." In Encyclopedia of Psychopharmacology. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_3001.

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Canary, James W., Yihan Wang, Richard Roy, Lawrence Que, and Hiroyuki Miyake. "Tris[(2-Pyridyl)Methyl] Amine (TPA) and (+)-Bis[(2-Pyridyl)methyl]-1-(2-Pyridyl)-Ethylamine (α-Metpa)." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132630.ch11.

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Gangjee, Aleem, Farahnaz Mavandadi, and Sherry F. Queener. "Synthesis and Biological Activity of Tricyclic, Conformationally Restricted Analogs of Lipophilic Pyrido[2,3-d]-Pyrimidine Antifolates." In Advances in Experimental Medicine and Biology. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-2960-6_88.

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Gangjee, Aleem, Anil Vasudevan, and Sherry F. Queener. "Bicyclic Conformationally Restricted Analogs of Nonclassical Pyrido[2,3-d] Pyrevddines as Potential Inhibitors of Dihydrofolate Reductases." In Advances in Experimental Medicine and Biology. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-2960-6_90.

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Makkar, Harinder P. S., P. Siddhuraju, and Klaus Becker. "L-Mimosine (β-(3-Hydroxy-4-Pyridone-1-yl)-L-Alanine)." In Plant Secondary Metabolites. Humana Press, 2007. http://dx.doi.org/10.1007/978-1-59745-425-4_8.

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Fischer, Sophia, Bertold Spiegelhalder, and Rudolf Preussmann. "No Pyrosynthesis of N′-Nitrosonornicotine (NNN) and 4-(Methylnitrosamino)-1-(3-Pyridyl)-1-Butanone (NNK) from Nicotine." In Effects of Nicotine on Biological Systems. Birkhäuser Basel, 1991. http://dx.doi.org/10.1007/978-3-0348-7457-1_14.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) complex of 5-(α-pyridyl)-1-phenylpent-1-yne-3, 5-dione." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_322.

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Conference papers on the topic "Pyrido[1"

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Manabe, S., H. Yanagisawa, S. Ishikawa, et al. "TRYPTOPHAN PYROLYSIS PRODUCTS FOUND IN COOKED FOODS INHIBIT HUMAN PLATELET AGGREGATION BY INHIBITING CYCLOOXYGENASE." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643402.

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Humans are exposed to numerous toxic compounds in foods. During the past decade, several carcinogenic heterocyclic amines have been reported to be present in the cooked foods. Recently, we reported that some of the carcinogenic heterocyclic amines isolated from foods were present in human plasma. In order to know the effects of the carcinogens isolated from foods on the cell function, we investigated the effects of the carcinogenic heterocyclic amines including Trp-P-1(3-amino-l,4-dimethyl-5H-pyrido❘4,3-b❘indole) and Trp-P-2(3-amino-1-methyl-5H-pyrido❘4,3-b❘indole) on human platelet aggregatio
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Abass, Mohamed, and Aisha Mayas. "Substituted Pyridopyrimidinones. 1. Convenient PTC Alkylation and Halogenation of 2-Hydroxy-4H-pyrido[1,2-a]pyrimidin-4-one." In The 9th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2005. http://dx.doi.org/10.3390/ecsoc-9-01462.

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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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Öner, Nazmiye, Ömer Tamer, Davut Avci, and Yusuf Atalay. "A theoretical study on 3-(4-methoxyphenyl)-1-(pyridin-2-Yl) prop-2-en-1-one." In 9TH INTERNATIONAL PHYSICS CONFERENCE OF THE BALKAN PHYSICAL UNION (BPU-9). AIP Publishing LLC, 2016. http://dx.doi.org/10.1063/1.4944226.

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Gowdahalli, Krishnegowda, Arun K. Sharma, Jacek Krzeminski, et al. "Abstract 1700: An improved synthesis and mutagenicity studies ofO2-[4-(3-pyridyl-4-oxobut-1-yl]thymidine, the major adduct formed by tobacco-specific nitrosamine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK)in vivo." In Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-1700.

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Reddy, B. R., P. Venkateswarlu, and M. C. George. "Optical phase-conjugate studies of organic dyes." In OSA Annual Meeting. Optica Publishing Group, 1990. http://dx.doi.org/10.1364/oam.1990.fd4.

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Abstract:
We have investigated several organic dyes in an effort to identify new nonlinear-optical substances because these substances are of current scientific interest owing to their possible applications in several areas. Some of the dyes investigated are 21,71-dichlorofluorescein (DCF), rhodamine 110 (R110) and pyridin 1—all doped in boric acid host. The concentration of the dyes is 10−3-10−4 M and the thickness of the samples is ~100 µm. Degenerate four-wave mixing experiments, using multimode Argon ion laser wavelengths, have been performed on these samples to generate phase-conjugate (PC) signals
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Ashmore, Joseph, Ying Liu, Amity Peterson, Sabrina Fechtner, Gang Chen, and Philip Lazarus. "Abstract 2722: Characterization of human lung enzymes involved in the reduction of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK)." In Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-2722.

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Öner, Nazmiye, Ömer Tamer, Adil Başoğlu, Davut Avcı, and Yusuf Atalay. "Density functional theory calculations on (2e)-3-(3-Bromo-4-methoxyphenyl)-1-(pyridin-2-yl) prop-2-en-1-one." In TURKISH PHYSICAL SOCIETY 32ND INTERNATIONAL PHYSICS CONGRESS (TPS32). Author(s), 2017. http://dx.doi.org/10.1063/1.4976468.

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Yim, S., and S. Que Hee. "293. Mutagenicity of N'-Nitrosonornicotine (NNN), 4-(Methylnitrosamino)-1-(3-Pyridyl)-1-Butanone (NNK), and Anabasine in the Bacterial Bioluminescence Test." In AIHce 1997 - Taking Responsibility...Building Tomorrow's Profession Papers. AIHA, 1999. http://dx.doi.org/10.3320/1.2765427.

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Wang, Linxiao, Jianqiang Wang, Shan Xu, Jielian Wu, Qidong Tang, and Pengwu Zheng. "Synthesis of 3- morpholin-4-yl-1- (4-nitrophenyl) -5,6-dihydro -1H- pyridin-2-one." In 2016 4th International Conference on Machinery, Materials and Computing Technology. Atlantis Press, 2016. http://dx.doi.org/10.2991/icmmct-16.2016.149.

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