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Relevant bibliographies by topics / 6-dione

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Academic literature on the topic '6-dione'

Author: Grafiati

Published: 4 June 2021

Last updated: 27 April 2022

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Journal articles on the topic "6-dione"

1

Yanni, Amal S. "Heterocyclic quinones: Synthesis of some new heterocyclic quinones from 6-chloroquinoline-5,8-dione hydrochloride." Collection of Czechoslovak Chemical Communications 56, no. 9 (1991): 1919–25. http://dx.doi.org/10.1135/cccc19911919.

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Interaction of 6-chloroquinoline-5,8-dione hydrochloride with amides and/or thioamides in ethylene glycol afforded oxazolo[5,4-g]quinoline-4,9-dione (III) and thiazolo[5,4-g]quinoline-4,9-dione (V). Using semicarbazide and/or thiosemicarbazide in the above reaction, oxadiazino-, and thiadiazino[6,5-g]quinoline-5,10-diones (VI, VII), respectively, were obtained. Their bactericidal activities have been determined.

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2

Chung, Cheng-Yen, Ching-Chun Tseng, Sin-Min Li, Shuo-En Tsai, Hui-Yi Lin, and Fung Fuh Wong. "Structural Identification between Phthalazine-1,4-Diones and N-Aminophthalimides via Vilsmeier Reaction: Nitrogen Cyclization and Tautomerization Study." Molecules 26, no. 10 (2021): 2907. http://dx.doi.org/10.3390/molecules26102907.

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N-Aminophthalimides and phthalazine 1,4-diones were synthesized from isobenzofuran-1,3-dione, isoindoline-1,3-dione, furo [3,4-b] pyrazine-5,7-dione, or 1H-pyrrolo [3,4-c] pyridine-1,3-dione with monohydrate hydrazine to carry out the 5-exo or 6-endo nitrogen cyclization under the different reaction conditions. Based on the control experimental results, 6-endo thermodynamic hydrohydrazination and kinetical 5-exo cyclization reactions were individually selective formation. Subsequently, Vilsmeier amidination derivatization was successfully developed to probe the structural divergence between N-

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Yanni, Amal S., Zarif H. Khalil, and Ahmed A. Timmawy. "Synthesis of some new sulfonamide derivatives of 7-chloroquinoline-5,8-dione and pyridocarbazolediones." Collection of Czechoslovak Chemical Communications 56, no. 7 (1991): 1489–94. http://dx.doi.org/10.1135/cccc19911489.

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Interaction of 6-chloroquinoline-5,8-dione hydrochloride (I) or 6,7-dichloroquinoline-5,8-dione (II) with sulfa drug in ethanol containing diethylaniline afforded 7-substituted sulfonamide-10H-pyrido[3,2-b]carbazole-5,11-dione (III), and sulfonamide derivatives of 7-chloroquinoline-5,8-diones (IV). Moreover the reaction of II with arylamine in pyridine afforded substituted 6H-pyrido[2,3-b]carbazole-5,11-dione (V). The structure of the compounds was determined by elemental and spectral analysis, and by chemical reaction.

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Farkens, Michael, Ion Neda та Reinhard Schmutzler. "Zur Chemie der 1,3,5-Triaza-2-phosphorinan-4,6-dione. Teil VIII. Weitere 1,3,5-Triaza-2 λ3-und 1,3,5-Triaza-2 λ4-phosphorinan-4,6-dione mit (2-Chlorethyl)amino-und Bis(2-chlorethyl)amino-Substituenten / Chemistry of the 1,3,5-Triaza-2-phosphorinan-4,6-diones. Part VIII. Further 1,3,5-Triaza-2λ3- and 1,3,5-Triaza-2λ4-phosphorinane-4,6-diones with (2-Chloroethyl)amino- and Bis(2-chloroethyl)amino Substituents". Zeitschrift für Naturforschung B 49, № 4 (1994): 445–50. http://dx.doi.org/10.1515/znb-1994-0403.

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In the reaction of 2-chloro-1,5-dimethyl-3-phenyl-1,3,5-triaza-2λ3-phosphorinane-4,6- dione (1) and 2-chloro-1,3,5-triphenyl-1,3,5-triaza-2λ3-phosphorinane-4,6-dione (2) with (2-chloroethyl)amine hydrochloride or bis(2-chloroethyl)amine hydrochloride in the presence of triethylamine the corresponding (2-chloroethyl)amino- and bis(2-chloroethyl)amino-substituted 2λ3-phosphorinane-4,6-diones (3-6) are formed. Oxidation with the hydrogen peroxide- urea-1: 1-adduct gives the corresponding 2-oxo-2λ4-phosphorinane-4,6-diones (7-10), in the same manner as described in the literature for the 1,3,5-tri

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5

Journal, Baghdad Science. "Synthesis & Characterization of Oxazinan and 5-oxa-7-aza-spiro[2,5] octane from reaction of Dibenzylidene with malonic anhydride and 5-oxa-spiro[2,3] hexane-4,6-dione." Baghdad Science Journal 4, no. 2 (2007): 276–84. http://dx.doi.org/10.21123/bsj.4.2.276-284.

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Di Benzylidenes were prepared by condensation of 1,2-diamino benzene with o- hydroxy benzaldehyde. These dibenzylidenes when treated with one equivalent of malonic anhydride or 5-oxo-spiro[2,3]hexane-4,6-dione in dry benzene give 6-membered heterocyclic ring system of 3-{2-[(2-Hydroxy-benzylidene)-amino]-phenyl}-2-(2-hydroxy –phenyl)-[1,3]oxazinane-4,6-diones ( 1-3) or 7-{2-[(2-hydroxy-benzylidene)-amino]-phenyl}-6-(2-hydroxy-phenyl)-5-oxa-7-aza-spiro[2.5]octane-4,8-diones ( 7- 9 ) But when two equivalents of malonic anhydride or 5-oxo-spiro[2,3]hexane-4,6-dione were used and under sam conditi

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6

Slater, Kara A., Brad Andersh, Edward B. Flint, and Gregory M. Ferrence. "6-Phenyloxane-2,4-dione." Acta Crystallographica Section E Structure Reports Online 69, no. 1 (2012): o69. http://dx.doi.org/10.1107/s1600536812049781.

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Marcuccio, SM, and JA Elix. "Pyrazine Chemistry. IV. Oxidation of 3,6-Dibenzylpiperazine-2,5-diones." Australian Journal of Chemistry 38, no. 2 (1985): 343. http://dx.doi.org/10.1071/ch9850343.

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The autoxidation of (�) cis- and trans-3,6-dibenzyl-1,4- dimethylpiperazine-2,5-diones (6) and (8) has been shown to give (�)-6- benzyl-1,4-dimethylpiperazine-2,3,5-trione (12). Oxidation of a (2) cis-trans mixture of 1,4-diacetyl-3,6-dibenzylpiperazine-2,5-diones, (5) and (7), with elemental sulfur was shown to give (�)-(Z)-1-acetyl- 6-benzyl-3-benzylidenepiperazine-2,5-dione (10).

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Aesha F SH Abdassalam, Aesha F. SH Abdassalam, Semih Kurban Semih Kurban, and Nahide Gulsah Deniz and Cigdem Sayil Nahide Gulsah Deniz and Cigdem Sayil. "Synthesis and Characterization of New Naphtho- and Tetracyclic Diazaquinone Derivatives." Journal of the chemical society of pakistan 41, no. 5 (2019): 834. http://dx.doi.org/10.52568/000805/jcsp/41.05.2019.

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In this study, new 1,4-naphtho- and 5-nitro-1,4-naphtho derivatives containing N- and N,N-substituted groups which has not been reported yet, have been synthesized from 2,3-dichloronaphthalene-1,4-diones (1,9). Compounds of 2-choloro-3-((2,4,6-triflorophenyl)amino)naphthalene-1,4-dione (3) and 2-chloro-3-((4-florophenyl)amino)naphtalene-1,4-dione (7) were obtained by reactions of 2,3-dichloronaphthalene-1,4-dione 1 with 4-fluoroaniline (6) and 2,4,6-trifloroaniline (2), respectively involving a Michael addition. We reported the cyclization reactions of compounds 1 to benzo[g]pirido[3,2-b]quino

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Yoneyama, Koichi, Makoto Konnai, Tadao Asami, Nobutaka Takahashi, and Shigeo Yoshida. "Photosystem II Inhibition by 3-Acyl-5-(l-aminoalkylidene)-4-hydroxy- 2H -pyran-2,6(3H)-dione Derivatives." Zeitschrift für Naturforschung C 45, no. 11-12 (1990): 1127–32. http://dx.doi.org/10.1515/znc-1990-11-1208.

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3-Acyl-5-(1-aminoalkylidene)-4-hydroxy-2 H- pyran-2,6(3 H)-dione derivatives carrying lipophilic amino groups were found to be highly potent inhibitors of photosynthetic electron transport, and both the acyl and the aminoalkylidene groups on the pyran ring appeared to be indispensable for high activity. The structural features needed for activity in the 3-acyl-5- (l-am inoalkylidene)-4-hydroxy -2 H-pyran -2 ,6 (3 H)-dione derivatives were very similar to those for 3 -(l-aminoalkylidene)-2H-pyran-2,4(3H)-diones, except for the acyl group in the former compounds. Thermoluminescence measurements

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Vyas, Vijyesh K., and Bhalchandra M. Bhanage. "Asymmetric transfer hydrogenation of seven membered tricyclic ketones: N-substituted dibenzo[b,e]azepine-6,11-dione driven by nonclassical CH/O interactions." Organic Chemistry Frontiers 3, no. 5 (2016): 614–19. http://dx.doi.org/10.1039/c6qo00036c.

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Enantioselective transfer hydrogenation of dibenzo-fused-azepine-diones: N-substituted dibenzo[b,e]azepin-6-11-dione was achieved by ruthenium catalysis in the presence of formic acid/triethylamine as a mild hydrogen source.

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Dissertations / Theses on the topic "6-dione"

1

Botella, Jacqueline. "Interactions de l'acétate de nomegestrol 17 alpha-acétoxy-6 alpha-méthyl-19-norpregna-4,6-diene-3,20-dione avec les récepteurs des hormones stéroïdes chez le rat in vitro, ex vivo." Grenoble 2 : ANRT, 1988. http://catalogue.bnf.fr/ark:/12148/cb37612086m.

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Renard, Annabelle. "Synthèse d'analogues spiraniques de nucléosides et leur incorporation dans des oligonucléotides." Université Joseph Fourier (Grenoble), 1999. http://www.theses.fr/1999GRE10031.

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Notre projet consiste a developper un nouveau type d'oligonucleotides modifies constitue d'un enchainement de spironucleosides, potentiellement capable de reconnaitre des sequences d'adn double brin en formant une triple helice. Nous avons choisi comme premieres unites a incorporer, les desoxyhydantocidines dh# et dh# et les nucleosides spirobarbituriques sb et cb. Ces spironucleosides presentent egalement un interet potentiel en tant que nouveaux analogues de nucleosides biologiquement actifs. Nous avons developpe une voie de synthese efficace des deux epimeres de desoxyhydantocidine dh# et d

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Gomez, Catherine. "Elaboration de nouveaux inhibiteurs mixtes ECA/ECE pour le traitement de l'hypertension." Phd thesis, Université d'Orléans, 2008. http://tel.archives-ouvertes.fr/tel-00465126.

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Les inhibiteurs mixtes de l'ECE et de l'ECA constituent une classe thérapeutique originale qui intervient dans la régulation de l'hémodynamique, en bloquant en amont la production de puissants vasoconstricteurs tels que l'angiotensine II et l'endothéline-1. Ces deux peptides sont générés, respectivement, grâce à l'enzyme de conversion de l'angiotensine II et de l'endothéline-1. En inhibant leur action, les agents thérapeutiques mixtes récents (1970) prennent ainsi une part importante dans le traitement de l'hypertension. Le premier type d'inhibiteurs porte un groupement phosphoré qui se lie au

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4

Oliveira, José Flávio Tenório de. "Determinação das Estruturas Cristalinas e Moleculares dos Compostos: 4-hidroxi 6 propenil 5,6 diidro-piran-2-ona; 4 metoxi 6 fenil 5,6-diidro piran 2 ona; 6,6-difenil diidro piran 2,4 diona e 5,6 difenil diidro piran 2,4 diona, Utilizando Técnicas de Difração de Raios X." Universidade Federal de Alagoas, 2006. http://repositorio.ufal.br/handle/riufal/1087.

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This work presents a study developed on four composites dihydro pyranc , (4 hydroxy 6 propenyl 5,6 dihydro pyran 2-one ; 4-metoxy 6 phenyl 5,6 dihydro pyran 2-one; 6,6 diphenyl-dihydro pyran 2,4-dione; 5,6 diphenyl dihydro pyran 2,4-dione), respectively called in this work (unofficial) forms f1, f2, f3 e f4. These compounsds were synthesized by Msc Laura Cristiane de Souza on the LaSO laboratory of Universidade Federal de Alagoas (UFAL), which is supervised by Prof. Dr. Dennis de Oliveira Imbrosi. The collected intensities had been measured using radiation monochromatot by a graphite crystal

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Mongin, Olivier. "Synthèse de molécules naturelles par métallation de diméthoxypyridines." Rouen, 1994. http://www.theses.fr/1994ROUES062.

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Ce travail décrit la préparation et la métallation des 2,3- et 3,4-diméthoxypyridines, ainsi que de la 3,4-diméthoxypyridine-N-oxyde. Ces résultats ont été utilisés pour la synthèse de molécules douées d'une activité biologique: à partir des 3,4-diméthoxypyridines, nous avons préparé une nouvelle azaxanthone, ainsi que l'orelline et un composé analogue de cet alcaloïde naturel, par association des réactions de métallation et d'homocouplage. A partir de 2,3-diméthoxypyridine, outre la préparation de la partie pyridinique des Piéricidines, nous décrivons la première synthèse de deux autres moléc

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Cimatti, Helen Mariana Baldan [UNESP]. "Farmacocinética pré-clínica e avaliação toxicológica do novo composto α2-adrenérgico 3-(2-cloro-6-fluorobenzil)-imidazolidina-2,4-diona - PT-31 GIRSUPAN". Universidade Estadual Paulista (UNESP), 2013. http://hdl.handle.net/11449/132772.

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Made available in DSpace on 2016-01-13T13:27:56Z (GMT). No. of bitstreams: 0 Previous issue date: 2013-09-19. Added 1 bitstream(s) on 2016-01-13T13:33:28Z : No. of bitstreams: 1 000856429.pdf: 1307975 bytes, checksum: 34294ec81a6d27dee7b8b875a152935a (MD5)<br>Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)<br>Instituto Nacional de Ciência e Tecnologia para inovação farmacêutica (INCT-if )<br>O composto 3-(2-cloro-6-fluorobenzil)-imidazolidina-2-4-diona - PT-31 GIRSUPAN, planejado pelo grupo de pesquisa da Universidade Federal de Pernambuco, apresenta perfil analgésico re

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Cimatti, Helen Mariana Baldan. "Farmacocinética pré-clínica e avaliação toxicológica do novo composto α2-adrenérgico 3-(2-cloro-6-fluorobenzil)-imidazolidina-2,4-diona - PT-31 GIRSUPAN /". Araraquara, 2013. http://hdl.handle.net/11449/132772.

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Orientador : Rosângela Gonçalves Peccinini<br>Banca: Roberto Takashi Sudo<br>Banca: Thalita Pedroni Formariz Pilon<br>Banca: Jean Leandro dos Santos<br>Banca: Chung Man Chin<br>Resumo: O composto 3-(2-cloro-6-fluorobenzil)-imidazolidina-2-4-diona - PT-31 GIRSUPAN, planejado pelo grupo de pesquisa da Universidade Federal de Pernambuco, apresenta perfil analgésico resultante da ativação do 2-adrenoceptor no sistema nervoso central. Ainda, quando administrado pela via intraperitoneal (i.p.), em camundongos (15 mg/kg), o produto apresenta efeito sinérgico com a morfina. O objetivo desse estudo fo

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Cheng, Ying-Geh, and 陳瑩潔. "Synthesis and Biological Activity of N-substituted benzyl-6(7 or8)-bromo-2,3,4,9-tetrahydrofuro[2,3-b]quinolin-3,4-dione." Thesis, 2001. http://ndltd.ncl.edu.tw/handle/16930729796111369129.

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碩士<br>中國醫藥學院<br>藥物化學研究所<br>89<br>A series of N-substituted benzyl-6( 7or 8 )-bromo-2, 3, 4, 9-tetra- hydrofuro[2,3-b]quinolin-3,4-diones has been synthesized and assigned by their spectra data. All of these synthetic compounds were evaluated for antiallergic and antiinflammatory activity by inhibition tests of mast cell degranulation, neutrophil degranulation , and neutrophil superoxide formation. Among these 6-substitute compounds, N-p-methylbenzyl-6-bromo- 2,3,4,9- tetrahydrofuro[2,3-b]quinolin-3,4-dione (9)exhibited inhibitory activity on fMLP-induced neutrophil degranulation .

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Chien, Ching-Ming, and 簡啟民. "Cytotoxic mechanisms of Cardiotoxin III (CTX III)、N′-(11H-indolo[3,2-c]quinolin-6-yl)-N,N-dimethylethane-1,2-diamine (IQDMA) and Naphtho[1,2-b]furan-4,5-dione (NFD)." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/85029628380595944153.

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博士<br>高雄醫學大學<br>醫藥暨應用化學研究所<br>98<br>Apoptosis plays an important role in the regulation of cellular activities in eukaryotes. Three predominant apoptotic pathways are the mitochondria-mediated intrinsic pathway, the death receptor-induced extrinsic pathway and apoptotic signalling evoked by endoplasmic reticulum (ER) stress. Three type of compounds (CTX III, IQDMA and NFD)-induced apoptotic cell death accompanied by regulation of Bcl-2 family, loss of mitochondrial membrane potential, release of cytochrome c and caspase-9, -3 activation. In addition, CTX III induced ER stress, release of Ca2+

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Hsin-Yi, Wei, and 魏欣怡. "Study on Nylon 6 Synthesis via Anionic Polymerization Using Azetidine-2,4-diones as the Activators." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/77557112602501694593.

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碩士<br>國立中興大學<br>化學工程學系<br>93<br>This research focused on the study of anionic ring-opening polymerization of caprolactum to synthesize Nylon 6 using structurally varied azetidine-2, 4-diones as the activators. The polymerizations were carried out by a one-step melt-process to find out the effects of activator’s concentration, types (aromatic or aliphatic), functionalities ( n=1 and 2), substituents (on azetidine-2,4-dione ring) as well as those of reaction temperature on polymerization rates. The aim is to find the best activator and optimal condition for possible application in reaction injec

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Books on the topic "6-dione"

1

Krapinger, Gernot. Dion Chrysostomos oratio 6: Text, Übersetzung, Einleitung und Kommentar. Verlag für die Technische Universität Graz, 1996.

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United States. Congress. Senate. Committee on Armed Services. Nominations before the Senate Armed Services Committee, second session, 108th Congress: Hearings before the Committee on Armed Services, United States Senate, One Hundred Eighth Congress, second session, on nominations of Francis J. Harvey; Lawrence T. Di Rita; William A. Chatfield; Tina Westby Jonas; Dionel M. Aviles; Jerald S. Paul; Mark Falcoff; GEN George W. Casey, Jr., USA; ADM Vernon E. Clark, USN; Lt. Gen. James E. Cartwright, USMC; VADM Timothy J. Keating, USN; LTG Bantz J. Craddock, USA; Peter Cyril Wyche Flory; Valerie Lynn Baldwin; Dr. Francis J. Harvy; Richard Greco, Jr.; Gen. Gregory S. Martin, USAF; Joseph F. Bader; R. Bruce Matthews; Otis W. Brawley; and Vinicio E. Madrigal, January 28, February 4, April 27, May 11, June 24, July 8, 21, October 6, November 17, 2004. U.S. G.P.O., 2005.

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Anthony, Bells. Notebook Journal Lined: DIONNE Quote Personalized Name Funny Birthday Gift Idea 6 X 9 Lined Composition Notebook Gift for Teachers Lined Notebook for Neos, Officers, ... Diary. Independently Published, 2020.

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Book chapters on the topic "6-dione"

1

Inoue, M., C. Cruz-Vázquez, M. B. Inoue, K. W. Nebesny, and Q. Fernando. "Preparation of Electroconducting Materials Containing Copper Compounds: A Copper Oxide with 1,3,4, 6-Tetrathiapentalene-2,5-dione." In Springer Proceedings in Physics. Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-75424-1_12.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of diaqua-bis(1, 3, 6, 7-tetramethylpteridine-2, 4-(1H, 3H)-dione)nickel(II) perchlorate." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_558.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of diaqua-bis(1, 3, 6, 7-tetramethylpteridine-2, 4-(1H, 3H)-dione)cobalt(II) perchlorate." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_299.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of diaqua-bis{1, 3, 6, 7-tetramethylpteridine-2, 4-(1H, 3H)-dione}copper(II) nitrate dihydrate." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_60.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of diaqua-bis{1, 3, 6, 7-tetramethylpteridine-2, 4-(1H, 3H)-dione}nickel(II) nitrate dihydrate." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_561.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of diaqua-bis{1, 3, 6, 7-tetramethylpteridine-2, 4-(1H, 3H)-dione}cobalt(II) nitrate dihydrate." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_306.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of diaqua-bis(1, 3, 6, 7-tetramethylpteridine-2, 4-(1H, 3H)-dione-O4, N5)manganese(II) perchlorate." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_574.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of diaqua-bis(1, 3, 6, 7-tetramethylpteridine-2, 4-(1H, 3H)-dione-O4, N5)copper(II) perchlorate dihydrate." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_52.

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Schomburg, Dietmar, and Ida Schomburg. "cyclohexane-1,2-dione hydrolase 3.7.1.11." In Class 3.4–6 Hydrolases, Lyases, Isomerases, Ligases. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-36260-6_26.

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Wohlfarth, Ch. "Dielectric constant of the mixture (1) pentane-2,4-dione; (2) bromobenzene." In Supplement to IV/6. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75506-7_848.

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Conference papers on the topic "6-dione"

1

Hoffmann, Guenter G. "Fourier transform infrared and FT-Raman spectra of (+)-5, 6, 7, 8-tetrahydro-8-methylindan-1,5-dione." In Fourier Transform Spectroscopy: Ninth International Conference, edited by John E. Bertie and Hal Wieser. SPIE, 1994. http://dx.doi.org/10.1117/12.166737.

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Park, Eun-Jung, Andrew Morrell, Martin Conda-Sheridan, Mark Cushman, and John M. Pezzuto. "Abstract 1934: Characterization of the anti-proliferative effect of 6-(3-aminopropyl)-9-methoxy-3-nitro-5H-indeno[1,2-c]isoquinoline-5,11(6H)-dione in cultured PC-3 cells." 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.am2012-1934.

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Zarins, Elmars, Julija Pervenecka, Elina Misina, et al. "Glassy 2-(1-benzyl-2-styryl-6-methylpyridin-4(1H)-ylidene) fragment containing 1H-indene-1,3(2H)-dione and pyrimidine-2,4,6(1H,3H,5H)-trione derivatives with light-emitting and amplified spontaneous emission properties." In Fiber Lasers and Glass Photonics: Materials through Applications II, edited by Stefano Taccheo, Maurizio Ferrari, and Jacob I. Mackenzie. SPIE, 2020. http://dx.doi.org/10.1117/12.2553687.

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Mishra, Jibanananda, and Berrin Serdar. "Abstract 1789: Effects of benzo(a)pyrene-7,8-dione and cadmium on early response to DNA damage in primary human bronchoepithelial cells." In Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-1789.

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