Relevant bibliographies by topics / NITROSO DERIVATIVES

Contents

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

Academic literature on the topic 'NITROSO DERIVATIVES'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "NITROSO DERIVATIVES"

1

R., Jeyaraman, C. Thenmozhiyal J., Murugadoss R., and Muthukumar M. "Stereodynamics of diheteroarylpiperidines and their derivatives." Journal of Indian Chemical Society Vol. 76, Nov-Dec 1999 (1999): 527–36. https://doi.org/10.5281/zenodo.5861764.

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Department of Chemistry, Bharathidasan University, Tiruchirappalli-620 024, India <em>Manuscript received 10 August 1999</em> The stereodynamics of a number of <em>N</em>-nitroso-<em>cis</em>-<em>r</em>-2,<em>c</em>-6-di(2-hctcroaryl)- and <em>N</em>-nitroso-<em>cis</em>-<em>r</em>-2,<em>c</em>-6-diarylpiperidines (12-17) have been studied. The conformational preferences have been correlated with those of <em>N</em>-nitroso-<em>cis</em>-<em>r</em>-2,<em>c</em>-6-dimethylpiperidine (1) and <em>N</em>-nitroso-<em>cis</em>-<em>r</em>-2,<em>c</em>-6-diphenylpiperidines (2a-f, 3a-e). Competition be
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Wu, Yinuo, Ling-Jun Feng, Xiao Lu, Fuk Yee Kwong, and Hai-Bin Luo. "Palladium-catalyzed oxidative C–H bond acylation of N-nitrosoanilines with toluene derivatives: a traceless approach to synthesize N-alkyl-2-aminobenzophenones." Chem. Commun. 50, no. 97 (2014): 15352–54. http://dx.doi.org/10.1039/c4cc07440h.

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A palladium-catalyzed cross-coupling of N-nitroso-anilines and toluene derivatives for the direct synthesis of N-alkyl-2-aminobenzophenones is described. N-nitroso could act as the traceless directing groups.
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Abdelhamid, Abdou Osman, and A. S. Shawali. "Synthesis of Some New 2-Imino-2,3-dihydro-1,3,4-thiadiazole and Selenadiazole Derivatives." Zeitschrift für Naturforschung B 42, no. 5 (1987): 613–16. http://dx.doi.org/10.1515/znb-1987-0516.

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(2)Diazotized 3(5)amino-5(3)-phenylpyrazole reacts with phenacylthiocyanate (1) and phenacylselenocyanate (10) to give the corresponding 1,3,4-thiadiazoline derivative (5) and 1,3,4- selenadiazoline derivative (12), respectively. A mechanism is proposed and it is substantiated by an alternate synthesis of 5 and 12 from the corresponding hydrazidoyl bromide (6) with potassium thiocyanate and potassium selenocyanate, respectively. The thiadiazoline (5) and selenadiazoline (12) give the respective N-acyl derivatives (7a) and (12) with acetic anhydride. Nitrosation of 5 and 12 gives the correspond
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Попов, В. О., В. Н. Комов, Е. М. Попенко, and А. В. Сергиенко. "NON-ISOTHERMAL KINETICS OF SOLID-PHASE DECOMPOSITION OF MIXTURES OF OCTOGEN WITH NITRO-NITROZOAMINES." Южно-Сибирский научный вестник, no. 6(40) (December 20, 2021): 193–98. http://dx.doi.org/10.25699/sssb.2021.40.6.022.

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Определены формально-кинетические характеристики термораспада нитро-нитрозоаминов и их смесей с октогеном. Реакция разложения нитрозоаналогов октогена и нитро-нитрозопроизводных тетраазадекалина характеризуется меньшей энергией активации по сравнению с октогеном, и протекает с большей скоростью. Проведен анализ активационных параметров термораспада смесей, установлено активирующее влияние нитрозопроизводных тетраазадекалина на разложение октогена. The formal-kinetic characteristics of the thermal decomposition of nitro-nitrosoamines and their mixtures with HMX have been determined. The decompo
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Quesada, Antonio, Antonio Marchal, Manuel Melguizo, et al. "Amino-substituted O6-benzyl-5-nitrosopyrimidines: interplay of molecular, molecular-electronic and supramolecular structures." Acta Crystallographica Section B Structural Science 58, no. 2 (2002): 300–315. http://dx.doi.org/10.1107/s0108768101021607.

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The structures of eight 2,4,6-trisubstituted-5-nitrosopyrimidines (one of which crystallizes in two polymorphs) have been determined, including seven O6-benzyl derivatives which are potential, or proven, in vitro inhibitors of the human DNA-repair protein O6-alkylguanine-DNA-transferase. In the derivatives having an amino substituent at the 4-position, an intramolecular N—H...O hydrogen bond with the nitroso O as an acceptor leads to an overall molecular shape similar to that of substituted purines. There is a marked propensity for these nitroso compounds to crystallize with Z′ = 2. The struct
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Pinter, A., G. B. Spiegelhalder, G. Török, et al. "Genotoxicity of N-nitroso-piperazine derivatives." Toxicology Letters 95 (July 1998): 44–45. http://dx.doi.org/10.1016/s0378-4274(98)80175-6.

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Sonnenschein, Kristina, Herbert de Groot, and Michael Kirsch. "Formation ofS-Nitrosothiols from Regiospecific Reaction of Thiols withN-Nitrosotryptophan Derivatives." Journal of Biological Chemistry 279, no. 44 (2004): 45433–40. http://dx.doi.org/10.1074/jbc.m405987200.

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S-nitrosothiols transport nitric oxidein vivo, and so-called transnitrosation reactions (i.e.the transfer of the nitroso function from nitrosothiol to thiolate) are believed to be involved in this process. In the present study we examined theN-nitrosotryptophan derivative-dependent nitrosation of thiols, a hitherto ignored possibility for the formation ofS-nitrosothiols. The corresponding products were identified by15N-NMR spectrometry. The fact that the reaction proceeded under hypoxic conditions as well as in non-aqueous solution strongly indicated the occurrence of a transnitrosation reacti
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Abele, Edgars, and Ramona Abele. "Oximes of Nucleosides and Related Compounds: Synthesis, Reactions and Biological Activity." Current Organic Synthesis 15, no. 5 (2018): 650–65. http://dx.doi.org/10.2174/1570179415666180524112811.

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Background: Literature data on the synthesis and structure of oximes of nucleosides and related nitrogenous bases from pyrimidine and purine were reviewed. Synthesis of novel heterocyclic systems from nucleoside oximes related pyrimidine oximes was described. The biological activity of derivatives of nucleoside and nitrogenous base oximes was also reviewed. &lt;p&gt; Objective: The review focuses on the recent progress in the area of nucleoside oxime synthesis, reactions and biological activity. Conclusion: In summary, literature data on the synthesis and structure of oximes of nucleosides and
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Monbaliu, Jean-Christophe M., Lucas K. Beagle, Judit Kovacs, Matthias Zeller, Christian V. Stevens та Alan R. Katritzky. "En route towards α-benzotriazoyl nitroso derivatives". RSC Advances 2, № 24 (2012): 8941. http://dx.doi.org/10.1039/c2ra21311g.

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El-Kashef, Hussein, Talaat El-Emary, Pierre Verhaeghe, Patrice Vanelle, and Maha Samy. "Anticancer and Anti-Inflammatory Activities of Some New Pyrazolo[3,4-b]pyrazines." Molecules 23, no. 10 (2018): 2657. http://dx.doi.org/10.3390/molecules23102657.

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New derivatives of pyrazolo[3,4-b]pyrazines and related heterocycles were synthesized using 5-amino-3-methyl-4-nitroso-1-phenyl-pyrazole (1) as a starting material. The 5-acetyl derivative 15 was shown to be a useful key intermediate for the synthesis of several derivatives of pyrazolopyrazines. Some of the prepared compounds were evaluated for their anti-inflammatory and anti-breast cancer MCF-7 cell line activities. SAR study showed that compounds 15 and 29 exhibited remarkable anti-inflammatory activity, where 15 showed the same activity as that of the reference drug indomethacin. On the ot
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Dissertations / Theses on the topic "NITROSO DERIVATIVES"

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Chalton, Michael Allen. "Nitroso derivatives of l,3-dithiol-2-ylidenes, and related systems." Thesis, Durham University, 1996. http://etheses.dur.ac.uk/5295/.

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A range of substituted l,3-dithiol-2-ylidene systems have been prepared. These species have, subsequently, been converted to nitroso derivatives. The role of the 4-, 5- and ylidene subtituents in stabilising the nitroso-alkene moiety thus obtained has been investigated. X-ray molecular crystal data which show that these species are stabilised by intramolecular interactions are presented. Conversion of the nitroso derivatives to their thionitroso analogues has been attempted, but was unsuccessful. A selection of l-(l,3-dithiol-2-ylidene)-prop-2-ene systems have been prepared. These systems have
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Kerim, Mansour Dolé. "Des réactions multicomposants aux réactions de Tsuji-Trost des dérivés nitrés et phosphorylés." Thesis, Université Paris-Saclay (ComUE), 2018. http://www.theses.fr/2018SACLX115/document.

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Les travaux de cette thèse ont porté sur le développement de nouvelles méthodes de synthèse autour de la chimie des réactions multicomposants et des réactions de Tsuji-Trost des dérivés nitrés et phosphorylés. Dans le chapitre I, nous avons développé une nouvelle voie d’accès aux indoles propargyliques impliquant des adduits A3 et une réaction d’élimination d’amine en présence du 1,2-dibromoethane. Dans le chapitre II, nous avons démontré la possibilité d’exploiter des réactions de Tsuji-Trost par la formation de produits O-allylés issus des α-hydroxyphosphonates. La méthatèse cyclisante appli
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Jia, Shuanglong. "Multicomponent Reactions toward Heterocycles and Tsuji-Trost Reaction of Allylic Nitro Derivatives." Thesis, Université Paris-Saclay (ComUE), 2018. http://www.theses.fr/2018SACLY012/document.

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Les réactions multicomposantes jouent un rôle important en chimie organique. Ce sont des réactions qui mettent en jeu au moins trois réactifs de départ et qui permettent d’obtenir des produits considérés comme des éléments intéressants pour la synthèse de molécules complexes ou de composés bioactifs. Grâce à leur versatilité, ces réactions sont considérées comme des outils précieux pour la préparation de bibliothèques de composés organiques dans le domaine de la recherche pharmaceutique et de la synthèse de produits naturels.La réaction de Passerini, combinée à une addition de Michael et à une
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Jia, Shuanglong. "Multicomponent Reactions toward Heterocycles and Tsuji-Trost Reaction of Allylic Nitro Derivatives." Electronic Thesis or Diss., Université Paris-Saclay (ComUE), 2018. http://www.theses.fr/2018SACLY012.

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Les réactions multicomposantes jouent un rôle important en chimie organique. Ce sont des réactions qui mettent en jeu au moins trois réactifs de départ et qui permettent d’obtenir des produits considérés comme des éléments intéressants pour la synthèse de molécules complexes ou de composés bioactifs. Grâce à leur versatilité, ces réactions sont considérées comme des outils précieux pour la préparation de bibliothèques de composés organiques dans le domaine de la recherche pharmaceutique et de la synthèse de produits naturels.La réaction de Passerini, combinée à une addition de Michael et à une
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Sancibrao, Pierre. "Cycloadditions de nitroso Diels-Alder asymétriques et régiosélectives : une nouvelle voie synthétique d'hétérospirocycles." Thesis, Paris 11, 2012. http://www.theses.fr/2012PA112417.

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Au cours de ce projet de recherche, nous nous sommes intéressés à la synthèse de motifs hétérospiraniques énantioenrichis. De ce fait, notre équipe a pu élaborer une nouvelle voie synthétique pouvant conduire à la synthèse de molécules possédant des structures bicycliques spiraniques diverses. Cette voie de synthèse inédite est articulée sur une réaction de nitroso Diels-Alder. Le contrôle de la stéréosélectivité ainsi que le contrôle de la régiosélectivité, peu décrit dans la littérature, ont été spécifiquement étudiés lors de ces travaux. Nos différentes études ont permis de mieux appréhende
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Adam, David. "The synthesis and characterisation of halogen and nitro phenyl azide derivatives as highly energetic materials." Diss., lmu, 2001. http://nbn-resolving.de/urn:nbn:de:bvb:19-1842.

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Viswanathan, Subha. "Nitro- and oxazoline-derivatized antennas structural and photophysical characterization of their lanthanide complexes /." Related electronic resource:, 2007. http://proquest.umi.com/pqdweb?did=1362530571&sid=2&Fmt=2&clientId=3739&RQT=309&VName=PQD.

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Mishra, S. K. "Detection and analysis of spin trapped radical adducts by using alpha-phenyl-tert-butyl nitrone (PBN) derivatives and GC/MS." Thesis, University of Salford, 2016. http://usir.salford.ac.uk/39302/.

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Murray, Paul Ross. "Electrochemical and spectroelectrochemical studies on nitro-substituted poly-pyridine derivatives and their transition metal co-ordination complexes." Thesis, University of Edinburgh, 2005. http://hdl.handle.net/1842/11208.

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El, Berjawi Rayane. "Construction and characterizations of new perylenediimide based molecular assemblies derived from nitro or amino bay-substituted derivatives." Thesis, Angers, 2019. http://www.theses.fr/2019ANGE0062.

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Les dérivés de pérylènediimide (PDI) font partie des accepteurs d’électrons les plus performants. Leur squelette rigide liéà un système π aromatique étendu, des propriétés optiques et électroniques remarquables et une bonne stabilité chimique et thermique en font de bons candidats comme matériaux de type-n avec de nombreuses applications, en particulier dans le domaine du photovoltaïque organique. Ce travail étudie la réactivité de dérivés pérylènediimides en position «bay» pour la synthèse et la caractérisation de nouveaux systèmes accepteurs originaux dont certains seront utilisés comme maté
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Books on the topic "NITROSO DERIVATIVES"

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Boyer, Joseph H. Nitroazoles: The C-nitro derivatives of five-membered N- and N,O- heterocycles. VCH Publishers, 1986.

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Dimashki, Marwan. Characterisation, concentrations and phase distribution of polycyclic aromatic hydrocarbons (PAH) and their nitrated derivatives (Nitro-PAH) in the urban atmosphere. University of Birmingham, 1998.

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Patai, Saul. Chemistry of Amino Nitroso and Nitro Compounds and Their Derivatives: Supplement F, Part 1. Wiley & Sons, Limited, John, 2010.

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Stylianou, Akis Damianou. Studies of nitroso derivatives of amino acids. 1986.

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Patai, Saul. Chemistry of Amino Nitroso and Nitro Compounds and Their Derivatives: Supplement F, Part 2. Wiley & Sons, Limited, John, 2010.

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Nitro Compounds and Their Derivatives in Organic Synthesis. MDPI, 2020. http://dx.doi.org/10.3390/books978-3-03943-149-6.

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Boyer, Jospeh H. Nitroazoles: The C-Nitro Derivatives of Five-Membered N- And N, O-Heterocycles. Vch Pub, 1987.

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Book chapters on the topic "NITROSO DERIVATIVES"

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Atwood, Jim D., and Jerome B. Keister. "In Nitrosyl Derivatives." In Inorganic Reactions and Methods. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145296.ch31.

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Gouzerh, P., Y. Jeannin, A. Proust, F. Robert, and S. G. Roh. "Functionalization of Polyoxomolybdates: the Example of Nitrosyl Derivatives." In Topics in Molecular Organization and Engineering. Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0920-8_9.

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Fiedler, Heidelore, and Wolfgang Mücke. "Nitro Derivatives of Polycyclic Aromatic Hydrocarbons (NO2-PAH)." In The Handbook of Environmental Chemistry. Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-540-46757-1_2.

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De Sarlo, Francesco, and Fabrizio Machetti. "Condensation of Primary Nitro Compounds to Isoxazole Derivatives: Stoichiometric To Catalytic." In Methods and Applications of Cycloaddition Reactions in Organic Syntheses. John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118778173.ch08.

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Wortham, H. M., P. A. Masclet, and G. Mouvier. "Identification of Polycyclic Aromatic Nitro Derivatives during a Winter Photochemical Episode in Paris." In Physico-Chemical Behaviour of Atmospheric Pollutants. Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0567-2_91.

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Page, E. M., and D. A. Rice. "Synthesis of Metal Carbonyl Haiides and Nitrosyl Halides from the Metal Carbonyls and Their Derivatives." In Inorganic Reactions and Methods. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145180.ch159.

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Mizrahi, Jacques, Robert J. Bache, Eberhard Bassenge, et al. "Coronary Haemodynamic Profile of the New Nitro-Ester Derivative ITF 296 in the Conscious Dog." In Biochemical, Pharmacological, and Clinical Aspects of Nitric Oxide. Springer US, 1995. http://dx.doi.org/10.1007/978-1-4615-1903-4_10.

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Porta, Francesca, and Stefano Tollari. "Iron(III) and Manganese(III) Tetra-Arylporphyrins Catalyze the Oxidation of Primary Aromatic Amines to the Corresponding Nitro Derivatives." In The Activation of Dioxygen and Homogeneous Catalytic Oxidation. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-3000-8_66.

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Aitken, R. A., and K. M. Aitken. "With Benzotriazole Derivatives." In Nitro, Nitroso, Azo, Azoxy, and Diazonium Compounds, Azides, Triazenes, and Tetrazenes. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-041-00236.

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Cordero, F. M., and S. Cicchi. "Reactions with Nitroso Compounds." In Three Carbon-Heteroatom Bonds: Amides and Derivatives; Peptides; Lactams. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-022-00401.

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Conference papers on the topic "NITROSO DERIVATIVES"

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"N-Nitroso-BODIPY derivatives as effective light activated NO donors." In Bioinformatics of Genome Regulation and Structure/Systems Biology (BGRS/SB-2022) :. Institute of Cytology and Genetics, the Siberian Branch of the Russian Academy of Sciences, 2022. http://dx.doi.org/10.18699/sbb-2022-458.

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Agafonova, N. A., E. V. Shchegolkov, Ya V. Burgart, V. I. Saloutin, and M. V. Ulitko. "Synthesis of biological active compounds based on trifluoromethylcontaining 4-nitrosopyrazoles." In VIII Information school of a young scientist. Central Scientific Library of the Urals Branch of the Russian Academy of Sciences, 2020. http://dx.doi.org/10.32460/ishmu-2020-8-0009.

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e-pot nitrosation of 1,3-diketones or their lithium salts followed by treatment of hydrazines. Reduction of the nitroso-derivatives made it possible to obtain the 4-amino-3-trifluoromethylpyrazoles chlorides. Cytotoxic activity of the compounds wase evaluated in vitro
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Hawthorne, Steven B., Arnaud J. M. Lagadec, David J. Miller, and Peter J. Hammond. "Non-Oxidative Destruction of TNT, RDX, and HMX on Contaminated Soil Using Subcritical (Hot/Liquid) Water." In ASME 2003 9th International Conference on Radioactive Waste Management and Environmental Remediation. ASMEDC, 2003. http://dx.doi.org/10.1115/icem2003-4792.

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Subcritical (hot/liquid) water was used in a simple static (non-flowing) vessel to treat three soils from former defense sites which were contaminated with the explosives TNT (12 wt.%), or RDX (0.62 wt.%) and HMX (0.16 wt. %). Significant degradation of RDX began at 100 C, and at 125 C for TNT and HMX, with the bulk of the undergraded explosives remaining in the soil rather than in the water phase. Based on HPLC/UV analysis, intermediate degradation products formed, but quickly degraded at &lt; 250 C. Remediations performed using a generator-powered mobile pilot-scale unit (4 to 6 kg soil) wit
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Gribov, P., and A. Sheremetev. "N-CHLOROMETHYL NITRAMINE DERIVATIVES." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m761.aks-2019/235-236.

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Ustinov, Ilya, Nikolaj Khlytin, Yurij Atroshchenko, and Irina Shahkeldyan. "NEW THIAZOL DERIVATIVES CONTAINING NITRO QUINOLINE FRAGMENT." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m797.aks-2019/383-384.

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Kruglyakova, Lyudmila, Rudolf Stepanov, Konstantin Pekhotin, and Oksana Golubtsova. "THERMAL DECOMPOSITION OF SOME DINITROMETHANE DERIVATIVES." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m768.aks-2019/265-270.

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Astachov, Alexander, Denis Antishin, Svetlana Kapaeva, and Ekaterina Murashkina. "SYNTHESIS BENZYLNITROIMINO DERIVATIVES FROM S,S'-DIMETHYL-NNITROIMIDODIOCARBONATE." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m755.aks-2019/215-217.

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Gudkova, Inessa, and David Lempert. "SOME HYPOTETICAL TETRAZOLE DERIVATIVES AS COMPONENTS OF SOLID COMPOSITE PROPELLANTS." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m763.aks-2019/241-245.

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Ferry, Michael J., Ryan M. O’Donnell, Neal K. Bambha, Trenton R. Ensley, and William M. Shensky. "Analytical Characterization of Nitro-Derivatized Cyclometalating Ligands." In Frontiers in Optics. OSA, 2019. http://dx.doi.org/10.1364/fio.2019.jtu3a.26.

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Kepeňová, Martina, Michaela Benediková, Mária Vilková, Miroslava Litecká, and Ivan Potočňák. "Ionic palladium(II) complexes with nitro and halogen derivatives of 8-hydroxyquinoline." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.443k.

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Four commercially unavailable derivatives of 8-hydroxyquinoline with different functional groups (nitro and halogen) in positions 5 and 7 were prepared: 5-nitro-7-iodo-8-hydroxyquinoline (HNIQ), 5-nitro-7-bromo-8-hydroxyquinoline (HNBrQ), 5-iodo-7-bromo-8-hydroxyquinoline (HIBrQ) and 5-chloro-7-bromo-8-hydroxyquinoline (HClBrQ). Their characterization was performed by IR and NMR spectroscopy, elemental analysis and in the case of HIBrQ and HClBrQ by single crystal X-ray structure analysis. Prepared compounds were used for the synthesis of new palladium(II) complexes NH2(CH3)2[PdCl2(XQ)], where
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Reports on the topic "NITROSO DERIVATIVES"

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Lu, Q., and J. H. Boyer. Luminescent Nitro Derivatives of Benzotriazolo(2,1-a)Benzotriazole. Defense Technical Information Center, 1992. http://dx.doi.org/10.21236/ada251183.

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