Relevant bibliographies by topics / Nitroarene

Academic literature on the topic 'Nitroarene'

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Published: 10 March 2023

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Journal articles on the topic "Nitroarene"

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Xu, DaPeng, Meilu Xiong, and Milad Kazemnejadi. "Efficient reduction of nitro compounds and domino preparation of 1-substituted-1H-1,2,3,4-tetrazoles by Pd(ii)-polysalophen coated magnetite NPs as a robust versatile nanocomposite." RSC Advances 11, no. 21 (2021): 12484–99. http://dx.doi.org/10.1039/d1ra01164b.

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Facile nitroarene reduction as well as domino/reduction MCR preparation of 1-substituted-1H-1,2,3,4-tetrazoles from nitroarenes was performed by Pd(ii)-polysalophen coated magnetite NPs as a highly selective, recyclable and efficient nanocomposite.
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Loska, Rafał, and Mieczysław Mąkosza. "Introduction of Carbon Substituents into Nitroarenes via Nucleophilic Substitution of Hydrogen: New Developments." Synthesis 52, no. 21 (June 18, 2020): 3095–110. http://dx.doi.org/10.1055/s-0040-1707149.

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Nucleophilic substitution of hydrogen in nitroarenes has become a powerful synthetic tool for functionalization of these important organic substrates, complementary to other modern methods. In this review we present new developments in the area of introduction of alkyl and functionalized alkyl substituents into nitroarene rings via nucleo­philic substitution of hydrogen, followed by application of these processes in the construction of carbo- and heterocyclic rings. Finally, new developments in the investigation of the mechanism of SNArH are summarized.1 Introduction2 Alkylation and Haloalkylation3 Functionalized Carbon Substituents4 Formation of Carbo- and Heterocyclic Rings5 Mechanistic Aspects of SNArH6 Conclusion
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Lim, Taeho, and Min Su Han. "Preparation of Metal Oxides Containing ppm Levels of Pd as Catalysts for the Reduction of Nitroarene and Evaluation of Their Catalytic Activity by the Fluorescence-Based High-Throughput Screening Method." Catalysts 10, no. 5 (May 13, 2020): 542. http://dx.doi.org/10.3390/catal10050542.

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Herein, an easily accessible and efficient green method for the reduction of nitroarene compounds was developed using metal oxide catalysts. Heterogeneous metal oxides with or without Pd were prepared by a simple and scalable co-precipitation method and used for the reduction of nitroarenes. A fluorescence-based high-throughput screening (HTS) method was also developed for the rapid analysis of the reaction conditions. The catalytic activity of the metal oxides and reaction conditions were rapidly screened by the fluorescence-based HTS method, and Pd/CuO showed the highest catalytic activity under mild reaction conditions. After identifying the optimal reaction conditions, various nitroarenes were reduced to the corresponding aniline derivatives by Pd/CuO (0.005 mol% of Pd) under these conditions. Furthermore, the Pd/CuO catalyst was used for the one-pot Suzuki–Miyaura cross-coupling/reduction reaction. A gram-scale reaction (20 mmol) was successfully performed using the present method, and Pd/CuO showed high reusability without a loss of catalytic activity for five cycles.
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Lin, Yangming, Shuchang Wu, Wen Shi, Bingsen Zhang, Jia Wang, Yoong Ahm Kim, Morinobu Endo, and Dang Sheng Su. "Efficient and highly selective boron-doped carbon materials-catalyzed reduction of nitroarenes." Chemical Communications 51, no. 66 (2015): 13086–89. http://dx.doi.org/10.1039/c5cc01963j.

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Uberman, Paula M., Carolina S. García, Julieta R. Rodríguez, and Sandra E. Martín. "PVP-Pd nanoparticles as efficient catalyst for nitroarene reduction under mild conditions in aqueous media." Green Chemistry 19, no. 3 (2017): 739–48. http://dx.doi.org/10.1039/c6gc02710e.

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Jia, Wei-Guo, Tai Zhang, Dong Xie, Qiu-Tong Xu, Shuo Ling, and Qing Zhang. "Half-sandwich cycloruthenated complexes from aryloxazolines: synthesis, structures, and catalytic activities." Dalton Transactions 45, no. 36 (2016): 14230–37. http://dx.doi.org/10.1039/c6dt02734b.

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Marakatti, Vijaykumar S., and Sebastian C. Peter. "Nickel–antimony nanoparticles confined in SBA-15 as highly efficient catalysts for the hydrogenation of nitroarenes." New Journal of Chemistry 40, no. 6 (2016): 5448–57. http://dx.doi.org/10.1039/c5nj03479e.

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Moshapo, Paseka T., and Sandile B. Simelane. "Advances in nitroarene reductive amidations." Arkivoc 2020, no. 5 (February 10, 2021): 190–215. http://dx.doi.org/10.24820/ark.5550190.p011.417.

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Mondal, Manoj, Saitanya K. Bharadwaj, and Utpal Bora. "O-Arylation with nitroarenes: metal-catalyzed and metal-free methodologies." New Journal of Chemistry 39, no. 1 (2015): 31–37. http://dx.doi.org/10.1039/c4nj01293c.

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Laolob, Thanet, Nuntavan Bunyapraphatsara, Neti Waranuch, Sutatip Pongcharoen, Wikorn Punyain, Sirirat Chancharunee, Krisada Sakchaisri, et al. "Enhancement of Lipolysis in 3T3-L1 Adipocytes by Nitroarene Capsaicinoid Analogs." Natural Product Communications 16, no. 1 (January 2021): 1934578X2098794. http://dx.doi.org/10.1177/1934578x20987949.

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Transient receptor potential vanilloid 1 (TRPV1) activation by capsaicin binding increased intracellular calcium influx and stimulated adipocyte-to-adipocyte communication, leading to lipolysis. Generally, enhancement of π-stacking capabilities improves certain binding interactions. Notably, nitroarenes exhibit strong binding interactions with aromatic amino acid side chains in proteins. New capsaicinoid analogs were designed by substitution of the OCH3 group with a nitrogen dioxide (NO2) group on the vanillyl ring to investigate how π-stacking interactions in capsaicinoid analogs contribute to lipolysis. Capsaicinoid analogs, nitro capsaicin (5), and nitro dihydrocapsaicin (6) were prepared in moderate yields via coupling of a nitroaromatic amine salt and fatty acids. Oil Red O staining and triglyceride assays with 10 µM loading of capsaicin (CAP), dihydrocapsaicin (DHC), 5, and 6 were performed to investigate their effect on lipolysis in 3T3-L1 adipocytes. Both assay results indicated that 5 and 6 decreased lipid accumulation by 13.6% and 14.7%, respectively, and significantly reduced triglyceride content by 26.9% and 28.4%, respectively, in comparison with the control experiment. Furthermore, the decrease in triglyceride content observed in response to nitroarene capsaicinoid analogs was approximately 2-folds higher than that of CAP and DHC. These results arose from the NO2 group augmented π-π stacking with Tyr511 and the attractive charge interaction with Glu570 affecting binding interactions with TRPV1 receptors.
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Dissertations / Theses on the topic "Nitroarene"

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Udumula, Venkata Reddy. "Synthesis, RNA Binding and Antibacterial Studies of 2-DOS Mimetics AND Development of Polymer Supported Nanoparticle Catalysts for Nitroarene and Azide Reduction." BYU ScholarsArchive, 2015. https://scholarsarchive.byu.edu/etd/6031.

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Project I 2-Deoxystreptamine (2-DOS), the most conserved central scaffold of aminoglycosides, is known to specifically recognize the 5'-GU-'3 sequence step through highly conserved hydrogen bonds and electrostatic interactions within and without the context of aminoglycosides (Figure 1a). We proposed that a novel monomeric unnatural amino acid building block using 2-DOS as a template would allow us to develop RNA binding molecules with higher affinity and selectivity than those currently available. Conjugating two or more of the monomeric building blocks by an amide bond would introduce extra hydrogen bonding donors and acceptors that are absent in natural aminoglycosides and increase specificity of binding to a target RNA through a network of hydrogen bonds. In addition, the amide conjugation between the monomeric building blocks places two GU-base recognizing amines at 5 Å… distance, which is equal to the distance of neighboring base stacks in dsRNAs We hypothesized that targeting dsRNAs containing multiple consecutive 5'-GU-'3 sequence steps would become possible by connecting two or more of the monomeric building blocks by amide bonds. According to the proposed hypothesis, we designed three dimeric 2-DOS compounds connected by an amide bond. These three targets include the dimeric 2-DOS substrate connected by an amide bond, the dimeric 2-DOS containing the sugar moiety from Neamine, and a dimeric 2-DOS connected by a urea linker. These compounds were then tested for sequence specific binding against 8 different RNA strands, and for antibacterial activity against E. coli, actinobacter baumannii and klebsiella. Project II A dual optimization approach was used for to enhance the catalytic activity and chemoselectivity for nitro reduction. In this approach the composition of the nanoparticles and electronics effects of the polymer were studied towards nitro reduction. Bimetallic Ruthenium-Cobalt nanoparticles showed exceptional catalytic activity and chemoselectivity compared to monometallic Ruthenium nanoparticles. The electronic effects of the polymer also had a significant effect on the catalytic activity of the bimetallic nanoparticles. The electron-deficient poly(4-trifluoromethylstyrene) supported bimetallic nanoparticles undergo nitro reduction in 20 minutes at room temperature, whereas electron-rich poly(4-methylstyrene) and poly(4-methoxystyrene) supported bimetallic nanoparticles to longer reaction times to go to completion. Electronics of the polymers also effects the change in mechanism of nitroreduction. Polystyrene bimetallic Ruthenium-Cobalt nanoparticles showed excellent yields and chemoselectivity towards nitro functional group in the presence of easily reducible functional groups like alkenes, alkynes, allyl ethers, propargyl ethers. Monometallic ruthenium nanoparticles also showed excellent reactivity and chemoselectivity towards azide reduction in the presence of easily reducible functional groups. Interestingly monometallic ruthenium nanoparticles showed regioselective reduction of primary azides in the presence of secondary and benzylic azides, also aromatic azides can be selectively reduced in the presence of secondary azides. These polystyrene supported nanoparticles are heterogeneous and are easily separated from the reaction mixture and reused multiple times without significant of catalytic activity.
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Zhang, Yu-Feng. "Selective Electrocatalytic reduction mediated by Sm(II) : Application to nitroarenes, sulfoxides and phthalimides." Thesis, Université Paris-Saclay (ComUE), 2017. http://www.theses.fr/2017SACLS596/document.

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Le SmI₂ en tant que réactif de transfert monoélectronique a été largement utilisé en chimie organique depuis les premiers travaux de Kagan. Cependant, la quantité stœchiométrique ou en excès de SmI₂ et d'additifs toxique tels que HMPA sont utilisés normalement pour améliorer la réactivité. De plus, à cause de sa sensibilité à l'oxygène, le stockage de la solution de SmI₂ dans le THF est difficile. Récemment, nous avons développé une nouvelle méthode électrocatalytique basée sur la régénération électrochimique de Sm²⁺. Par rapport à la réactivité du SmI₂ classique, notre approche utilise une quantité catalytique de Sm. Premièrement, pour la réduction de nitroarènes, la réaction a sélectivement fourni les composés aromatiques azoïques et les anilines en fonction du solvant choisi. Notamment, c'est la première fois que la réaction Sm²⁺ se produit dans le méthanol dans le cas des anilines. Deuxièmement, dans le cas de la réduction des sulfoxydes par SmI₂, en général, l'HMPA était nécessaire comme additif. Dans notre procédé électrocatalytique, les sulfoxydes ont été transformés en sulfures avec une chimiosélectivité élevée et des excellents rendements toujours à température ambiante sans besoin ni de HMPA ni d’atmosphère protectrice. Enfin, les dérivés d'isoindolinone sont des séries de produits importants en chimie organique, la réduction des phtalimides est l'approche la plus pratique pour les obtenir. Avec les alcools, l'alcoxylation réductrice de phtalimides a eu lieu pour la première fois avec le Sm²⁺ électrocatalytique dans nos conditions. Et si on ajoute d'autres sources de protons, ce procédé a fourni les ω-hydroxylactames et isoindolinones correspondants avec des rendements élevés
The SmI₂ as a single electron transfer reagent has been widely used in organic chemistry since the pioneering works by Kagan. However, the stoichiometric or excess amount of SmI₂ and harmful additives such as HMPA are used normally to enhance the reactivity, moreover, due to the oxygen sensitive, the storage of SmI₂ solution is difficult.Recently, we have developed a new electrocatalytic method based on the electrochemical regeneration of Sm²⁺. Compared to the classic SmI₂ reaction, our process occurred with a catalytic amount of Sm. In the reduction of nitroarenes, it selectively afforded the azo aromatic compounds and anilines depending on different solvents system. Notably, it’s the first time that the Sm²⁺ reaction occurred in the methanol. Normally, the HMPA was the additive in the reduction of sulfoxides by SmI₂. Under our electrocatalytic process, the sulfoxides were converted into sulfides in high chemoselectivity and yield at room temperature without HMPA and protecting atmosphere.The isoindolinone derivatives are series of important products in organic chemistry, the reduction of phthalimides is the most convenient approach to provide them. With alcohols, the unprecedented Sm²⁺ electrocatalyzed reductive alkoxylation of phthalimides was established. Moreover, adding other proton sources, this process afforded the corresponding ω-hydroxylactams and isoindolinones
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Jones, Christopher Richard. "Biomonitoring of nitroarenes in Chinese workers." Thesis, University of Newcastle Upon Tyne, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.391964.

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Clarke, Ian Philip. "Old and new synthetic methodology with commercial applications." Thesis, University of Sunderland, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.311881.

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Davey, Claire Louise. "Reductions of aromatic carboxylic acids and nitroarenes using whole cell biotransformations." Thesis, University of Exeter, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.361337.

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RAMADAN, DOAA REDA MOHAMED. "PALLADIUM CATALYZED REACTIONS: REDUCTIVE CYCLIZATION OF NITROARENES, AND OXIDATIVE CARBONYLATION OF ANILINE." Doctoral thesis, Università degli Studi di Milano, 2021. http://hdl.handle.net/2434/819652.

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Palladium Catalyzed Reactions: Reductive Cyclization of Nitroarenes, and Oxidative Carbonylation of Aniline Abstract: The thesis is divided into two main chapters: reductive cyclization of nitroarenes, and oxidative carbonylation of aniline. The first chapter involves developing a catalytic system for carbazoles synthesis through reductive cyclization of 2-nitrobiphenyls employing phenyl formate as an in-situ source of CO. Thus, the synthetic chemist can avoid handling pressurized CO lines and perform the reaction in a pressure tube, a cheap and readily available tool for any laboratory. Moreover, the developed protocol can tolerate both air and moisture and can be performed using undried and undistilled commercial DMF. Several carbazoles bearing a wide range of substituents were synthesized in good to excellent yields including some with valuable pharmaceutical or thermo/electrical applications. The reaction could be performed on the grams scale affording carbazole in a very good yield (85%) without the need for chromatographic purification, making our synthetic strategy even more attractive and economically advantageous. The second chapter deals with the palladium/iodide couple which is the most investigated catalytic system for the oxidative carbonylation of amines to give ureas or carbamates. In reinvestigating it, we found that the most prominent role of iodide is to etch the stainless steel of the autoclave employed in most of previous works, releasing in solution small amounts of iron salts. The latter are much better promoters than iodide itself. Iron and iodide have a complex interplay and, depending on relative ratios, can even deactivate each other. The presence of a halide is beneficial, but chloride is better than iodide in this respect. The ideal Fe/Pd ratio is around 10, but even an equimolar amount of iron with respect to palladium (0.02 mol% with respect to aniline, corresponding to 12 ppm Fe with respect to the whole solution) is sufficient to boost the activity of the catalytic system. Such small amount may also come from Fe(CO)5 impurities present in the CO gas when stored in steel tanks. The role of the solvent has also been investigated. It was found that the reason for the better selectivity in some cases is at least in part due to a hydrolysis of the solvent itself, which removes the coproduced water.
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Akazome, Motohiro. "Studies on Transition-Metal Complex-Catalyzed Novel Transformation of Nitroarenes and Oximes by Deoxygenation Using Carbon Monoxide." Kyoto University, 1993. http://hdl.handle.net/2433/74623.

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Berson, Alain. "Mecanismes moleculaires de la toxicite hepatique des nitroarenes. Exemples du nilutamide et du flutamide, deux antiandrogenes non streroidiens." Paris 6, 1993. http://www.theses.fr/1993PA066702.

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La nadph-cytochrome p-450 reductase (ncpr) catalyse, dans les microsomes hepatiques, la reduction monoelectronique du nilutamide en un radical anion nitro. L'oxydation de ce radical par l'oxygene genere un cycle d'oxydoreduction formant des especes reactives de l'oxygene. Celles-ci entrainent un stress oxydatif responsable de la toxicite du nilutamide sur les hepatocytes isoles. Le nilutamide inhibe d'autre part le transfert des electrons au niveau du complexe un de la chaine respiratoire mitochondriale. Cet effet provoque une diminution de la formation d'atp responsable de la toxicite accrue du nilutamide sur les hepatocytes isoles incubes sans glucose. La ncpr ne catalyse pas la reduction monoelectronique du flutamide en un radical anion nitro. En revanche, les cytochromes p-450 appartenant aux familles 1a et 3a catalysent l'activation metabolique du flutamide en metabolite(s) reactif(s) qui consomment le glutathion et se fixent sur les proteines hepatiques. Le flutamide inhibe d'autre part le transfert des electrons au niveau des complexes un et deux de la chaine respiratoire mitochondriale. La formation de metabolites reactifs et l'inhibition de la respiration mitochondriale sont responsables de la toxicite du flutamide sur les hepatocytes isoles. La production d'intermediaires reactifs et la toxicite mitochondriale pourraient contribuer a expliquer la toxicite hepatique de ces deux nitroarenes utilises en clinique humaine dans le traitement des cancers metastases de la prostate
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Chapellas, Fabien. "Etude de cycloadditions tandem cascade [4+2] / [3+2] désaromatisante à partir de nitroarènes." Rouen, 2011. http://www.theses.fr/2011ROUES026.

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Les composés hétérocycliques aminés représentent une des plus importantes classes de structures d’intérêt pour la recherche pharmaceutique. Plus de 90% des composés dans ce domaine de recherche comportent au moins une de ces structures privilégiées. Parmi les méthodes les plus connues permettant l’accès aux composés aminés, la chimie des dérivés nitrés joue un rôle particulièrement important. Nous avons donc développé une réaction multicomposante activée par les hautes pressions au cours de laquelle un dérivé nitroaromatique réagit tout d’abord en tant qu’hétérodiène avec un diénophile enrichi électroniquement, dans une cycloaddition [4+2] à demande électronique inverse, pour générer un nitronate intermédiaire, qui lui-même réagit en tant que dipole dans une cycloaddition [3+2] subséquente menant au composé nitrosoacétalique. Ces composés sont d’intéressants motifs synthétiques, permettant un accès rapide aux composés hétérocycliques azotés après la rupture des liaisons N-O. Nous avons montré que la réaction pouvait être appliquée à un large panel de substrats nitroaromatiques. La cycloaddition [4+2]/[3+2] domino a ainsi été appliquée à plusieurs types de nitroaromatiques, tel que les indoles, thiophènes, benzofurannes, furannes, imidazoles, naphtalènes, et même au benzène. Les composés hétérocycliques aminés que nous pouvons générer par cette méthodologie comportent tous un carbone tétrasubsitué adjacent à l’atome d’azote. De tels motifs structuraux, sont difficiles d’accès par d’autres méthodes de synthèse. Notre méthode comporte l’avantage d’impliquer des réactifs de départ simples d’accès et de mener, en deux ou trois étapes seulement, aux composés désaromatisés polycycliques
Aminated heterocycles represent one of the most important structural classes of interest for the pharmaceutical research. More than 90% of the compounds in the field bear at least one of these “privileged-structures”. Among the oldest methods to get access to aminated molecules, those relying on the chemistry of nitro derivatives play a particularly important role. We thus have developed a multicomponent methodology in which, under hyperbaric activation, a nitroarene derivative first reacts as an inverse electron demand heterodiene with an electroenriched dienophile, to generate an intermediate nitronate that undergoes a subsequent [3+2] cycloaddition, leading to a nitrosoketal derivative. Such compounds are useful synthetic scaffolds, giving an easy access to nitrogenated motifs, after cleavage of the N-O bonds, for instance. We have shown that this domino [4+2]/[3+2] cycloaddition process can be applied to a wide panel of nitroaromatic substrates including indoles, thiophenes, benzofurans, furans, imidazoles, naphtalenes, and even benzene, for instance. The aminated compounds generated by this methodology all bear a tetrasubstituted center adjacent to the nitrogen atom. Such structural motifs are of difficult access by other synthetic methods. Our method thus bears the advantage of involving simple starting materials to lead, in two or three synthetic steps only, to dearomatized aminated polycycles
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Ceccarelli, Jacopo. "Nitrogen heterocycles: selective synthetic methods and applications." Doctoral thesis, 2020. http://hdl.handle.net/2158/1202776.

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On the basis the multifacet reactivity of the azaheterocycles, this thesis work is focused on the study of heterocyclic systems such as 1-(2-quinolyl)-2-propen-1-ol , phenyl(2-quinolyl)methanol, (2-quinolyl)(4-tolyl)methanol, and 3-methyl-4-nitro-5-(trichloromethyl)isoxazole in different domains.
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Books on the topic "Nitroarene"

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Howard, Paul C., Stephen S. Hecht, and Frederick A. Beland, eds. Nitroarenes. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4615-3800-4.

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International Conference on N-Substituted Aryl Compounds: Occurrence, Metabolism, and Biological Impact of Nitroarenes (4th 1989 Cleveland, Ohio). Nitroarenes: Occurrence, metabolism, and biological impact. New York: Plenum Press, 1990.

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IARC Working Group on the Evaluation of Carcinogenic Risks to Humans. Diesel and gasoline engine exhausts and some nitroarenes. Lyon, France: World Health Organization, International Agency for Research on Cancer ; [Geneva, Switzerland] : Distributed for the International Agency for Research on Cancer by the Secretariat of the World Health Organization, 1989.

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International Conference on Carcinogenic and Mutagenic N-Substituted Aryl Compounds (3rd 1987 Dearborn, Mich.). Carcinogenic and mutagenic responses to aromatic amines and nitroarenes: Proceedings of the Third International Conference on Carcinogenic and Mutagenic N-Substituted Aryl Compounds, held April 25-28, 1987, in Dearborn Michigan. Edited by King Charles M. 1932-, Romano Louis James 1950-, and Schuetzle Dennis 1942-. New York: Elsevier, 1988.

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Howard, Paul C., Stephen S. Hecht, and Frederick A. Beland. Nitroarenes: Occurrence, Metabolism, and Biological Impact. Springer London, Limited, 2012.

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Howard, Paul C., Stephen S. Hecht, and Frederick A. Beland. Nitroarenes: Occurrence, Metabolism, and Biological Impact. Springer, 2012.

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Nitroarenes: Occurrence, Metabolism, and Biological Impact. Springer, 2011.

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(Editor), Paul C. Howard, Stephen S. Hecht (Editor), and Frederick A. Beland (Editor), eds. Nitroarenes: Occurence, Metabolism, Biological Impact (Environmental Science Research). Springer, 1991.

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(Editor), C. M. King, L. J. Romano (Editor), and D. Schuetzle (Editor), eds. Carcinogenic and Mutagenic Responses to Aromatic Amines and Nitroarenes. Elsevier, 1987.

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(Producer), WHO, ed. Vol 46 IARC Monographs: Diesel and Gasoline Engine Exhausts and Some Nitroarenes (Iarc Monographs). World Health Organisation, 1989.

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Book chapters on the topic "Nitroarene"

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Mauderly, Joe L., William C. Griffith, Rogene F. Henderson, Robert K. Jones, and Roger O. McClellan. "Evidence from Animal Studies for the Carcinogenicity of Inhaled Diesel Exhaust." In Nitroarenes, 1–13. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4615-3800-4_1.

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Broyde, S., B. E. Hingerty, R. Shapiro, and D. Norman. "Unusual Hydrogen Bonding Patterns in 2-Aminofluorene (AF) and 2-Acetylaminofluorene (AAF) Modified DNA." In Nitroarenes, 113–23. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4615-3800-4_10.

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Poirier, Miriam C., Nancy F. Fullerton, Henrik S. Huitfeldt, Beverly A. Smith, Henry C. Pitot, John M. Hunt, and Frederick A. Beland. "DNA Adduct Formation During Chronic Administration of an Aromatic Amine." In Nitroarenes, 125–33. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4615-3800-4_11.

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Shibutani, Shinya, Robert Gentles, and Francis Johnson. "Aerial Oxidation of Acetylaminofluorene-Derived DNA Adducts." In Nitroarenes, 135–47. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4615-3800-4_12.

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Maher, Veronica M., M. Chia-Miao Mah, Jia-Ling Yang, Nitai P. Bhattacharyya, and J. Justin McCormick. "Mutations and Homologous Recombination Induced by N-Substituted Aryl Compounds in Mammalian Cells." In Nitroarenes, 149–56. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4615-3800-4_13.

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Martin, Carl N., and Gary S. Jennings. "Comparison of the Mutagenic Potency of DNA Adducts Formed by Reactive Derivatives of Aflatoxin, Benzidine and 1-Nitropyrene in a Plasmid System." In Nitroarenes, 157–66. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4615-3800-4_14.

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Lambert, I. B., A. J. E. Gordon, T. A. Chin, D. W. Bryant, B. W. Glickman, and D. R. McCalla. "Mutations Induced in the lacI Gene of E. coli by 1-Nitroso-8-Nitropyrene and Furylfuramide: The Influence of Plasmid pKM101 and Excision Repair on the Mutational Spectrum." In Nitroarenes, 167–80. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4615-3800-4_15.

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Smith, Beverly A., Robert H. Heflich, Yoshinari Ohnishi, Akinobu Ohuchida, Takemi Kinouchi, Janice R. Thorton-Manning, and Frederick A. Beland. "DNA Adduct Formation by 1-Nitropyrene 4,5- and 9,10-Oxide." In Nitroarenes, 181–87. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4615-3800-4_16.

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Bond, James A., Charles E. Mitchell, Joe L. Mauderly, and Ronald K. Wolff. "Nitropolycyclic Aromatic Hydrocarbons and Diesel Exhaust: Potential Role of DNA Binding in Carcinogenicity." In Nitroarenes, 189–99. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4615-3800-4_17.

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Gallagher, J. E., M. J. Kohan, M. H. George, M. A. Jackson, and J. Lewtas. "Validation/Application of 32P-Postlabeling Analysis for the Detection of DNA Adducts Resulting from Complex Air Pollution Sources Containing PAHs and Nitrated PAHs." In Nitroarenes, 201–9. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4615-3800-4_18.

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Conference papers on the topic "Nitroarene"

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Davis, Lloyd L., and Kay R. Brower. "Shock-initiation chemistry of nitroarenes." In The tenth American Physical Society topical conference on shock compression of condensed matter. AIP, 1998. http://dx.doi.org/10.1063/1.55668.

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Kunichkina, Anna, Irina Proskurina, Aleksandr Kotov, and Аnton Shetnev. "METHODS FOR SYNTHESIS OF 2,1-BENZISOXAZOLES FROM NITROARENES." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m769.aks-2019/271-274.

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Reports on the topic "Nitroarene"

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Gibson, David T. Molecular Mechanisms of Nitroarene Degradation. Fort Belvoir, VA: Defense Technical Information Center, September 2002. http://dx.doi.org/10.21236/ada429262.

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