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Relevant bibliographies by topics / Pyrido[4

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Academic literature on the topic 'Pyrido[4'

Author: Grafiati

Published: 7 June 2025

Last updated: 2 August 2025

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Journal articles on the topic "Pyrido[4"

1

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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2

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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3

Koch, Pierre, Dieter Schollmeyer, and Stefan Laufer. "2-(4-Fluorophenyl)-3-(4-pyridyl)pyrido[2,3-b]pyrazine." Acta Crystallographica Section E Structure Reports Online 65, no. 10 (2009): o2512. http://dx.doi.org/10.1107/s1600536809037295.

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4

Koch, Pierre, Dieter Schollmeyer, and Stefan Laufer. "3-(4-Fluorophenyl)-2-(4-pyridyl)pyrido[2,3-b]pyrazine." Acta Crystallographica Section E Structure Reports Online 65, no. 10 (2009): o2546. http://dx.doi.org/10.1107/s1600536809037970.

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5

Deady, L. W., D. Ganame, N. H. Quazi, and S. D. Zanatta. "On The Synthesis of Pyridinylthiobarbituric Acids." Australian Journal of Chemistry 55, no. 4 (2002): 287. http://dx.doi.org/10.1071/ch02050.

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The reaction of N-(pyridin-3-yl) and -4-yl thiourea derivatives with malonyl dichloride in trifluoroacetic acid is shown to be an efficient synthesis of the corresponding thiobarbituric acids. The pyridin-2-yl analogue cleaved and produced, instead, 2-hydroxy-4H-pyrido[1,2a]pyrimidin-4-one.

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6

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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7

Andersen, Heidi Gade, David Kvaskoff, and Curt Wentrup. "Bisiminopropadienes R-N=C=C=C=N-R from Pyridopyrimidines." Australian Journal of Chemistry 65, no. 6 (2012): 686. http://dx.doi.org/10.1071/ch12039.

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Chlorination of the N,N′-di(2-pyridyl)malonamide 13a affords 2-chloro-8-methyl-4-(2-(4-picolinyl)imino-4H-pyrido[1,2-a]pyrimidine 17a. Flash vacuum thermolysis of 17a causes efficient ring opening to the valence-tautomeric ketenimine 18a/19a, elimination of HCl, and formation of the bis(4-methyl-2-pyridyl)iminopropadiene, R-N=C=C=C=N-R 20a.

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8

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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9

Sun, Yi, Wenfei Huang, Zhiqiang Li, Tao Wang, and Jin Luo. "Design, synthesis, and herbicidal activity of novel 2-(arylamino)-5-methyl-4-methylene-7-(methylthio)-4H-pyrido[4,3-d][1,3]oxazine-8-carbonitrile derivatives." Journal of Chemical Research 43, no. 3-4 (2019): 119–23. http://dx.doi.org/10.1177/1747519819845771.

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A series of 5-methyl-4-methylene-7-methylthio-2-arylmino-4 H-pyrido[4,3- d][1,3]oxazine-8-carbonitrile derivatives were synthesized via tandem aza-Wittig and annulation reactions with { N-[3-acetyl-5-cyano-2-methyl-6-(methylthio)pyridin-4-yl]imino}triphenylphosphorane and aryl isocyanate in dry dichloromethane. Their structures were clearly confirmed by infrared, 1H NMR, 13C NMR, high-resolution mass spectrometry, and X-ray single-crystal diffraction. All newly synthesized compounds were screened for herbicidal activities against monocotyledonous and dicotyledonous plants. The results indicate

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10

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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Dissertations / Theses on the topic "Pyrido[4"

1

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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2

White, David Charles. "Synthesis of 3-Aryl-2-(2-aryl-2-oxoethyl)pyrido[2,3-d]-4(3H)pyrimidones and 3-Aryl-2-(2-arylethenyl)pyrido[2,3-d]-4(3H)pyrimidones as Potential Antiepileptic Drugs." Thesis, Virginia Tech, 1997. http://hdl.handle.net/10919/46506.

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A series of 2-alkyl-3-arylpyrido[2,3-d]pyrimidones were synthesized for testing as potential antiepileptic drugs. The goal was to achieve better neurological activity and/or lower toxicity than displayed by a series of 2-alkyl-3-aryl-4(3H)-quinazolinones prepared previously in our research group. From the pharmacological testing data of these target compounds, we have found that the additional nitrogen at the C-8 position of the quinazolinone framework increased the anticonvulsant activity. However, the neurological toxicity increased as well. The anticonvulsant and neurotoxic activi

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3

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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4

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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5

Gallo, Sandrine. "Synthèse de nouveaux dérivés 4-O-, 4-S-, 4-NH-alkylés de la pyrido[3,2-g]quinoline : Etude de l'activité de réversion de la chloroquino-résistance chez Plasmodium falciparum et de la MDR en cancérologie." Aix-Marseille 2, 2004. http://www.theses.fr/2004AIX22951.

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6

Le, Falher Laetitia. "Préparation et dérivatisation de 4H-pyrido[e][1,3]oxazinones : une contribution à la diversité chimique." Thesis, Paris 6, 2014. http://www.theses.fr/2014PA066344.

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Ce manuscrit porte sur la synthèse et les applications d'une nouvelle série de composés hétéroaromatiques : les 4H-pyrido[e][1,3]oxazin-4-ones. La première partie de ce manuscrit présente la préparation de ces squelettes via une réaction d'O-arylation intramoléculaire. La seconde partie du manuscrit repose sur la réactivité de ces entités chimiques et de leur utilisation en tant qu'intermédiaires de synthèse. La fonctionnalisation des 4H-pyrido[e][1,3]oxazin-4-ones, via des réactions de couplage pallado-catalysées, a permis d'obtenir des systèmes polyfonctionnalisés plus complexes. Les pyrido-

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7

Landelle, Henriette. "Synthèse et étude physicochimique des pyridazino [4,5-b] carbazoles, benzofuro [3,2-f] phtalazines, pyrido [3', 4' : 4,5] furo [3,2-b] indoles, benzothiéno [2,3-g] cinnolines." Caen, 1988. http://www.theses.fr/1988CAEN4072.

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8

Hou, Geneviève. "Synthèse de pyrido et de thiénopyrimidin-4(3H)-ones et de leurs produits de réduction : intérêt potentiel de ces composés dans le traitement de la thrombose." Bordeaux 2, 1997. http://www.theses.fr/1997BOR2E001.

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9

Berzosa, Rodríguez Xavier. "Diseño y síntesis de una quimioteca de sistemas 5,6-dihidropirido[2,3-d]pirimidin-7(8H)-ona no sustituidos en C4 como inhibidores potenciales de tirosina quinasas." Doctoral thesis, Universitat Ramon Llull, 2010. http://hdl.handle.net/10803/9299.

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Les Tirosina Cinases (TKs) són un grup de Proteïna Cinases claus en la senyalització cel·lular. Aquestes Cinases estan implicades, entre d'altres, en processos de creixement tumoral, fet que fa que la recerca d'inhibidors de TKs sigui una àrea d'investigació molt important en química mèdica.<br/>En aquest context es desenvolupa el present treball en el qual es pretenen sintetitzar inhibidors potencials de Tirosina Cinases amb estructura 4-hidrogenpirido[2,3-d]pirimidínica. Molècules amb aquesta estructura han presentat elevada activitat com inhibidors de TKs pel que en primer lloc s'aborda la

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10

Angello, Nicholas. "Development of a One Pot [4+2]/r[4+2] 2-Pyridone Synthesis and the Fluorescence of 2-Pyridone Azafluorenones." W&M ScholarWorks, 2018. https://scholarworks.wm.edu/etd/1550153876.

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We report the concise synthesis of several tricyclic 2-pyridones via a one pot sequence involving an aldol condensation, alkene isomerization, intramolecular Diels-Alder cycloaddition, and selective retro-Diels-Alder cycloreversion. The starting materials are synthesized in one step from cheap and commercially available precursors. The intermediate [2.2.2]diazabicycloalkene cycloadducts can be isolated. The retro-Diels-Alder occurs at easily accessible temperatures due to base acceleration. Simple derivatization of the tricyclic products afforded azafluorenones with unprecedented fluorescent a

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Books on the topic "Pyrido[4"

1

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

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2

Erfanian-Abdoust, Houshang. [4 + 2]-Cycloadditionen von Carbo- und Hetero-Dienophilen an Pyrano- und Pyrido[3,4-b]indol-3-onen: Ein neuer Zugang zu selektiv funktionalisierten [b]anellierten Indolen und Carbazolen. 1991.

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3

Kumpf, Joachim. Versuche zur Darstellung von Pyridin-3,4-chinonen und Synthesen von 3-Hydroxy-4-pyridonen. 1999.

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4

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

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5

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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6

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[4"

1

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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2

Vittimberga, Bruno M., John Cosgrove, and Howard R. Heyman. "Photoinitiated Radical Reactions of l-(4′-Pyridyl)-4-Pyridone and its N-Protio and N-Methyl Derivatives. Dimerization and Polymerization Reactions." In Free Radicals in Synthesis and Biology. Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-0897-0_7.

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3

Butcher, Howard J., Everly B. Fleischer, E. L. Muetterties, E. J. Muetterties, and M. C. Muetterties. "α,β,γ,δ-Tetra(4-pyridyl)porphinezinc." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132432.ch45.

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4

Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron(II) complex with 2-(pyridin-2-ylamino)-4-(pyridin-2-yl)thiazole." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_35.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand copper(II) complex with pyridin-2,6-dicarboxylic acid-N-oxide and 1,2-bis(4-pyridyl)ethene." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_340.

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6

Pardasani, R. T., and P. Pardasani. "Magnetic properties of adipato-1,2-bis(4-pyridyl)ethanemanganese(II)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 1. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62478-4_198.

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7

Pardasani, R. T., and P. Pardasani. "Magnetic properties of chloro-4-(2-pyridyl)-1-(2, 4-dihydroxy- benzaldehyde)- 3-thiosemicarbazonatomanganese(II)." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_631.

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8

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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9

Pardasani, R. T., and P. Pardasani. "Magnetic properties of adipato-[1,2-bis(4-pyridyl)ethane]cobalt(II)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 2. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62466-1_203.

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10

Pardasani, R. T., and P. Pardasani. "Magnetic properties of palladium(II) complex with 4-(pyridin-4-yloxy)-2,2,6,6-tetramethyl-1-piperidinoxyl ligand." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_467.

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Conference papers on the topic "Pyrido[4"

1

Kanwal, Priyanka, Ravinder Kour, Hans Raj, Rakesh Sharma, and Pankaj Bandhoria. "Crystallographic structure analysis of 2,7-dimethyl-3-chloro-4H-pyrido[1,2-a] pyrimidin -4-one." In 3RD INTERNATIONAL CONFERENCE ON CONDENSED MATTER AND APPLIED PHYSICS (ICC-2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0002354.

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2

Abass, Mohamed, Aisha Mayas, Wafaa Abdel-Monem, and Mostafa Ismail. "Substituted Pyridopyrimidinones. Part III. Synthesis of Some Novel Ether Derivatives of 4H-Pyrido[1,2-a]pyrimidin-4-one." In The 13th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00178.

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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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4

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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5

Marchand, Pascal, Thierry Besson, Yvonnick Loidreau, Marie-Renée Nourrisson, Corinne Fruit, and Cécile Corbière. "Synthesis of potential bioactive benzo-, pyrido-, or pyrazinothieno[3,2-<em>d</em>]pyrimidin- 4-amine analogs of MPC-6827." In 6th International Electronic Conference on Medicinal Chemistry. MDPI, 2020. http://dx.doi.org/10.3390/ecmc2020-07391.

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Jordis, Ulrich, Klaus Gerdes, C. Kappe, and Jennifer Kremsner. "Development of Multi-Gram Scale Microwave Assisted Organic Synthesis (MAOS): Suzuki Coupling towards 2,4-Dimethyl-8-[2'-(2H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-5,8-dihydro-6H-pyrido[2,3-d]pyrimidin-7-one (Tasosartan)." In The 9th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2005. http://dx.doi.org/10.3390/ecsoc-9-01637.

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7

Kashman, Yoel, Avi Koller, Amira Rudi, and Marta Gravalos. "Synthesis And Electrophilic Substitution of Pyrido[2,3,4-kl]acridines." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01809.

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Menéndez, J., Eva Pascual-Alfonso, and Carmen Avendaño. "Synthesis of the pyrido[2,3,4-kl]acridine ring system common to several cytotoxic marine alkaloids." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01913.

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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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Nauwelaërs, Gwendoline C., Yijin Tang, Dan Gu, Valérie Fessard, Robert J. Turesky, and Sophie A. Langouët. "Abstract 5739: Characterization of the metabolism and DNA adduct formation of 2-amino-9H-pyrido[2,3-b]indole in human hepatocytes." In Proceedings: AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012; Chicago, IL. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.am2012-5739.

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