Relevant bibliographies by topics / Nitroso groups

Contents

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

Academic literature on the topic 'Nitroso groups'

Author: Grafiati
Published: 5 June 2025
Last updated: 15 July 2025

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Journal articles on the topic "Nitroso groups"

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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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Cikotiene, Inga, Mantas Jonusis, and Virginija Jakubkiene. "The first example of the Fischer–Hepp type rearrangement in pyrimidines." Beilstein Journal of Organic Chemistry 9 (September 6, 2013): 1819–25. http://dx.doi.org/10.3762/bjoc.9.212.

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A N-nitroso moiety can be used for the activation of chloropyrimidines toward a nucleophilic substitution reaction with amines. The subsequent treatment of the obtained products with aq H2SO4 can lead to either N-denitrosation to obtain 4,6-pyrimidinediamines or to a Fischer–Hepp type rearrangement to obtain 5-nitroso-4,6-pyrimidinediamines. It was found that the outcome of the reaction strongly depends on the structure of the pyrimidines. Activation of the pyrimidine ring by three groups with a positive mesomeric effect is crucial for the intramolecular nitroso group migration.
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Wang, Zean, Hao Liu, Kang Zhou, Peifang Fu, Hancai Zeng, and Jianrong Qiu. "Effect of surface oxygen/nitrogen groups on hydrogen chloride removal using modified viscose-based activated carbon fibers." RSC Advances 5, no. 105 (2015): 86006–12. http://dx.doi.org/10.1039/c5ra11705d.

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Evans, Anthony S., Andrew D. Cohen, Zachary A. Gurard-Levin, et al. "Photogeneration and reactivity of acyl nitroso compounds." Canadian Journal of Chemistry 89, no. 2 (2011): 130–38. http://dx.doi.org/10.1139/v10-101.

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Acyl nitroso compounds have been generated by photolysis of several different classes of precursors including 9,10-dimethylanthracene adducts, nitrodiazo compounds, and 1,2,4-oxadiazole-4-oxides. Consideration of the nitronate-like resonance structure of nitrodiazo compounds led to an examination of the photochemistry of nitronates with α-leaving groups. Photolysis of such nitronates has been shown to generate an acyl nitroso species along with a carbene intermediate. Nanosecond time-resolved infrared (TRIR) spectroscopy has been used to detect photogenerated acyl nitroso compounds directly and to examine their reaction kinetics with amines and thiols. The mechanism of acyl nitroso aminolysis by primary amines involves general base catalysis, while the mechanism of aminolysis by secondary amines is strictly bimolecular. Thiols do not seem to be reactive with acyl nitroso compounds on the microsecond time scale, but thiolates are quite reactive. The reaction between benzoyl nitroside and an organic-soluble thiolate, tetrabutylammonium dodecanethiolate, proceeds via a proposed tetrahedral intermediate, which is observable by TRIR spectroscopy.
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Cameron, Mailer, Brian G. Gowenlock, Giuseppe Vasapollo, et al. "Solid State Spectroscopic Studies of Molybdenum Oxo Species with Coordinated ONR Groups." Journal of Chemical Research 23, no. 6 (1999): 354–55. http://dx.doi.org/10.1177/174751989902300605.

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A re-investigation of some complexes of molybdenum claimed to contain coordinated C-nitroso compounds has demonstrated that these solids are complex and that π-coordination of RNO cannot be the sole structural component.
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Didukh, S. L., V. N. Losev, A. N. Mukhina, N. G. Maksimov, and A. K. Trofimchuk. "Adsorption-photometric determination of iron using silica with nitroso-R salt and nitroso-N salt functional groups." Journal of Analytical Chemistry 72, no. 1 (2017): 47–53. http://dx.doi.org/10.1134/s1061934817010051.

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Trofimchuk, A. K., S. L. Didukh, A. N. Mukhina, and V. N. Losev. "Preconcentration And Determination Of Nickel Ions Using Silica With Functional Groups Of Sulfonic Derivatives Of Nitroso Naphthols." Methods and Objects of Chemical Analysis Vol. 14, No.1 (2019): 30–36. http://dx.doi.org/10.17721/moca.2019.30-36.

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Silica based adsorbents modified with polyhexamethylene guanidine and sulfonic derivatives of nitroso naphthols - nitroso-N salt (NNS) and nitroso-R salt (NRS), have been proposed for preconcentration and solid-phase photometric determination of Ni(II) in industrial solutions. Adsorbents with the surface concentration of the reagents of 1.5 and 3 μmol/g have been studied. Adsorbents with NNS functional groups quantitatively extract Ni(II) at pH 5.5-7.5, while with NRS functional groups – at pH 5.5-7.0, giving complex compounds with the composition Ni(II) : Reagent = 1 : 3. After Ni(II) adsorption the adsorbents became orange (λ = 510 нм) or brown (λ = 490 нм) for NNS and NRS respectively. The pH range of maximum color intensity coincides with the pH range of the quantitative extraction of Ni(II). The procedure of solid-phase photometric determination of Ni(II) in form of diffuse reflectance spectroscopy has been developed. The analytical range of the procedure is 0.1 – 3.0 μg of Ni(II) per 0.1 g of the adsorbent with the surface concentration of the reagent of 1.5 μmol/g and 0.15 – 6 μg of Ni(II) per 0.1g of the adsorbent with the surface concentration of the reagent of 3 μmol/g. The procedure was used for determination of Ni(II) in the rinsing and waste waters of galvanic manufactory. The results accuracy was confirmed by ICP-OES analysis.
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Shim, Jae Ho, Ji Yeon Lee, Hyeon Soo Kim, and Deok-Chan Ha. "Protonated Chiral 1,2-Diamine Organocatalysts for N-Selective Nitroso Aldol Reaction." Catalysts 12, no. 4 (2022): 435. http://dx.doi.org/10.3390/catal12040435.

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The introduction of nitrogen to carbonyl groups is considered both challenging and highly desirable by those who work in the field of organic synthesis. In this study, a diphenylethylenediamine-derived catalyst demonstrating N-selectivity was designed using a quantum calculation for the nitroso aldol reaction. The reductive monoalkylation of (R,R)-(+)-1,2-diphenylethylenediamine afforded an organic chiral diamine catalyst in high yield. The expected reaction mechanism for the nitroso aldol reaction was determined, and the product and solvent conditions were optimized through quantum calculations. The calculation results revealed that the enantioselectivity is determined by the hydrogen bond between the alkyl substituent of the chiral diamine and the oxygen of the aromatic aldehyde on the ammonium moiety. The reaction was found to proceed optimally in the presence of 5 mol % catalyst at −10 °C in brine. Using these conditions, an eco-friendly nitroso aldol reaction was performed in which the organic catalyst and cyclohexanone formed enamine. Nitrosobenzene, activated by hydrogen bonding with an ammonium catalyst, was used to minimize the steric hindrance between the catalyst and the reactant, resulting in high enantioselectivity. A nitroso aldol product with high N-selectivity and enantioselectivity (98% ee) was obtained in 95% yield. The catalyst developed in this study provides a less expensive and more environmentally friendly alternative for the nitroso aldol reaction.
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Buca, Beatrice Rozalina, Liliana Mititelu-Tartau, Cristiana Filip, et al. "The Influence of Nitric Oxid Donors Nebivolol and S-Nitrosoglutathion of the Oxidatives Stress and Liver Function in Rats." Revista de Chimie 70, no. 4 (2019): 1360–63. http://dx.doi.org/10.37358/rc.19.4.7127.

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We aimed to investigate the influence of two nitric oxide donors on the oxidative stress and the liver function in rats with experimental-induced acute paw inflammation.The experiment was carried out on white male Wistar rats (200-250 g), randomly assigned into 4 groups of 5 animals each, which received the substances intraperitoneal, as follows: group 1 (Control) saline solution 0.1 ml/100 g body weight; group 2 (IND) indomethacin 150 mg/kg body weight (kbw); groups 3 (NEB) and 4 (GSNO) nebivolol 1 mg/kbw, respectively S-nitroso-glutathione 1 mg/kbw. Carrageenan-induced rat�s paw edema test was used for the generation of acute inflammation. The activity of liver enzymes and of some antioxidant parameters was evaluated before the carrageenan injection, after 24 hours and 3 days. The experimental protocol was approved by the University�s Ethic Committee on Research and Ethical Issues.The administration of indomethacin, nebivolol and S-nitroso-glutathione appears to decrease the oxidative stress after 24 h in rats with experimental-induced acute paw inflammation. The nitric oxide donors nebivolol and S-nitroso-glutathione produced moderate functional and structural liver disturbances in rats with acute inflammation.
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Rai, Kartik, Vincent Wu, Priya Gupta, David A. Laviska, and Benny C. Chan. "N-Methyl-N-nitroso-p-toluenesulfonamide." Acta Crystallographica Section E Structure Reports Online 70, no. 7 (2014): o782. http://dx.doi.org/10.1107/s1600536814013518.

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The crystal structure of the title compound, C8H10N2O3S, displays predominant C—H...O hydrogen-bonding and π–π stacking interactions. The hydrogen bonds are between the O atoms of the sulfonyl group and H atoms on methyl groups. The π–π stacking interactions occur between adjacent aromatic rings, with a centroid–centroid distance of 3.868 (11) Å. These interactions lead to the formation of chains parallel to (101).
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Dissertations / Theses on the topic "Nitroso groups"

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Richter-Addo, George Bannerman. "Synthetic utilization of the redox properties of some group 6 organometallic nitrosyl complexes." Thesis, University of British Columbia, 1988. http://hdl.handle.net/2429/29174.

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The redox behavior of a series of organometallic complexes containing Cp'M(NO) groups (Cp' = ƞ⁵-C₅H₅(Cp) or ƞ⁵-C₅Me₅(Cp*) ; M = Mo or W) has been investigated both by cyclic voltammetry and by chemical means. The neutral 16-electron Cp'Mo(N0)X₂ compounds (X = CL, Br or I) undergo a single, essentially reversible, one-electron reduction in CH₂CL₂/O.1M [n-Bu₄N]PF₆ at relatively low potentials (<-0.1 V vs SCE). The electrochemically observed reductions can be effected on a preparative scale by employing CP₂C0 as the chemical reductant. The isolable 17-electron [Cp'Mo (NO)X₂]•⁻ radical anions are cleanly reconverted to their 16-electron neutral precursors by treatment with [Cp₂Fe]BF₄. In contrast, the Cp'W(NO)I₂ compounds undergo rapid decomposition to their [Cp'W(NO)I]₂ monohalo dimers upon electrochemical reduction. Electrophiles NE⁺ (E = O or ϱ-O₂NC₆H₄N) undergo unprecedented insertions into the Cr-C ϭ-bonds of CpCr(NO)₂R complexes (R = Me, CH₂SiMe₃ or Ph) to afford [CpCr(N0)₂{N(E)R}]⁺ cationic complexes. Present evidence is consistent with these insertions occurring via charge-controlled, intermolecular attacks by NE⁺ at the Cr-R groups in classical SE2 processes. The newly-formed N(E)R ligands function as Lewis bases through nitrogen atoms toward the formally 16-electron [CpCr(NO)₂]⁺ cations and may be displaced from the chromium's coordination sphere by the more strongly coordinating CL⁻ anion. The resulting CpCr(NO)₂CL can be reconverted to CpCr(NO)₂R. thereby completing a cycle by regenerating the initial organometallic reactant. The entire sequence of stoichiometric reactions forming the cycle thus constitutes a selective method for the formation of new carbon-nitrogen bonds, the net organic conversions mediated by the CpCr(NO)₂ group being NE⁺ + R⁻ → N(E)R. The electrophilic [Cp'M(NO)₂]⁺ cations (Cp'=Cp or Cp* ; M = Cr, Mo or W) condense with methyl propiolate and 2,3-dimethyl-2-butene to afford cationic organometallic lactone complexes. These complexes undergo facile ⍜-dealkylation to yield the neutral Cp'M(NO)₂(ƞ¹-lactone) derivatives. Furthermore, the neutral Cp'W(NO)₂(ƞ¹-lactone) compounds decompose in air to their Cp'W(O)₂(ƞ¹-lactone) dioxo products.<br>Science, Faculty of<br>Chemistry, Department of<br>Graduate
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Sharp, William Brett. "Synthesis and ligand reactivity of group 6 organometallic nitrosyl complexes." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/NQ61173.pdf.

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Zhou, Yang. "DEVELOPMENT OF PHOTOACTIVATABLE NITROXYL (HNO) DONOR MOLECULES USING PHOTOLABILE PROTECTING GROUPS." Kent State University / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=kent1501350106636151.

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Scheibel, Markus. "Metal-Nitrogen Multiple Bonds with Square-Planar Group 9 Transition Metal PNP Pincer Complexes." Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2014. http://hdl.handle.net/11858/00-1735-0000-0023-9944-4.

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Formenti, D. "REDUCTIVE TRANSFORMATIONS OF THE NITRO GROUP: FROM HOMOGENEOUS TO HETEROGENEOUS CATALYSIS." Doctoral thesis, Università degli Studi di Milano, 2017. http://hdl.handle.net/2434/479447.

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This thesis focuses its attention into two different aspects of catalysis. In the first part, transition-metal complexes were used as homogeneous catalysts for the preparation nitrogen-containing heterocycles (especially indoles) using liquid sources of carbon monoxide. In the second part, in collaboration with Prof. Matthias Beller (Leibniz Institute for Catalysis-LIKAT, Rostock), doped-carbon heterogeneous non-noble metal catalysts were employed as catalytic materials in the hydrogenation of nitroaromatics. In both cases, nitro compounds were used as valuable starting materials corroborating their central role in organic chemistry. Equally, mechanistic aspects (especially kinetics) were taken into account showing how they can play a pivotal role in understanding not only the specific reaction mechanism but also how a catalytic system can be further improved.
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Peerless, B. "Synthesis, characterisation and reactivity of low-valent and hypercoordinate azido, triazenido and nitrato complexes of Group 14 and Group 15 elements." Thesis, University of Sheffield, 2017. http://etheses.whiterose.ac.uk/19019/.

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Kidwell, Andy R. "Factors influencing the metathesis of group VI transition metal complexes containing Nitrido and Alkylidyne Ligands." The Ohio State University, 2002. http://rave.ohiolink.edu/etdc/view?acc_num=osu1413370830.

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Hartdegen, Vera [Verfasser], and Thomas M. [Akademischer Betreuer] Klapötke. "Energetic polymers and plasticizers based on organic azides, nitro groups and tetrazoles : synthesis and characterization / Vera Hartdegen. Betreuer: Thomas M. Klapötke." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2016. http://d-nb.info/1105374033/34.

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Dursun, Hayrettin. "Determination Of The Postexplosion Residues Of Nitro Group Containing Explosives In Soil With Gc-ms And Gc-tea." Master's thesis, METU, 2007. http://etd.lib.metu.edu.tr/upload/2/12609014/index.pdf.

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There is an increase in bombing assaults in recent years in our country. Determining the explosive material used in these cases by the quick and correct analysis of the evidence obtained after the explosions, is an important starting point for the investigations which are done to reach the perpetrators. The forensic chemistry investigations have to be correct, exact and rapid in order to reach the right criminal. In this study, the Gas Chromatography-Mass Spectrometry (GC-MS) and Gas Chromatography-Thermal Energy Analyser (GC-TEA) methods which are being used for the determination of the explosive materials&rsquo<br>residues used in bombing attacks are optimized with the standard solutions of 2,4,6-Trinitrotoluene (TNT) and 1,3,5-trinitro-1,3,5-triazocyclohexane (RDX) and standard mixture solution. The two methods were compared by analysing the postexplosion soil samples. Also an efficient and applicable sample preparation procedure was developed. The results showed that both methods are efficient and sensitive for the postexplosion investigations. It is seen that GC-TEA has lower detection limit and simple chromatograms due to its selectivity against only nitro group containing explosives. However it is concluded that there is a need for a reliable and sensitive method like GC-MS which provides identification and library search, for the determination of the organic components which can not be identified with GC-TEA
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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 matériaux dans des cellules solaires organiques.Dans la première partie de cette thèse, une procédure alternative à la réaction de couplage type Suzuki-Miyaura a été développée pour la synthèse de dérivés PDI à partir du composépossédant un groupement nitro en position «bay». Une dyade associant le PDI au fullerène C60a ensuite été étudiée. Dans une seconde partie, l’étude s’est portée sur la synthèse et la caractérisation de nouveaux dimères de PDI et leurs utilisations comme matériaux dans des cellules solaires organiques. Dans le dernier chapitre, des recherches ont été menées sur la réactivité d’un PDI possédant un groupement amino en position «bay», d’abord via la chimie des sels de diazonium, puis dans la synthèse d’azacoronènes pour former de nouvelles dyades à base de PDI. Ces nouveaux composés ont fait l’objet d’études préliminaires comme nouveaux matériaux accepteurs pour des applications en photovoltaïque<br>Among the powerful organic electron acceptors are those based on perylenediimide derivatives. Their rigid planar backbone and extended π-conjugation with outstanding optical and electronic properties, chemical and thermal stabilities allowed them to be potentially useful as n-type materials in applications such as organic photovoltaic cells (OPVs).This dissertation describes the study of perylenediimide reactivity at the bay region for the synthesis and characterizations of new original acceptor systems. Some of them were applied in organic solar cells. In the first part of this thesis, an alternative procedure to conventional Suzuki-Miyaura coupling method was developed for the synthesis of PDI derivatives starting from mono-nitro PDI. From this was targeted the construction of PDI-C60dyad.In the second part, synthesis and characterizations of PDI dimer and its application in organic solar cells are discussed. In the last part, investigations on the reactivity of mono-amino PDI are described via the chemistry of the diazonium salt or through the synthesis of PDI-based azacoronene dyads. Preliminary studies of some of these acceptors in organic solar cells are also presented
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Books on the topic "Nitroso groups"

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Patai, Saul, ed. The Chemistry of Amino, Nitroso, Nitro and Related Groups. John Wiley & Sons, Ltd, 1996. http://dx.doi.org/10.1002/047085720x.

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Saul, Patai, ed. The chemistry of amino, nitroso, nitro, and related groups. Wiley, 1996.

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Great Britain. Working Party on Nitrate and Related Compounds in Food. and Great Britain. Ministry of Agriculture, Fisheries and Food., eds. Nitrate, nitrite and N-nitroso compounds in food: The twentieth report of the Steering Group on Food Surveillance, the Working Party on Nitrate and Related Compounds in Food. H.M.S.O., 1987.

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Steering Group on Chemical Aspects of Food Surveillance. Working Party on Nitrate and Related Compounds in Food. Nitrate, nitrite and n-nitroso compounds in food: Second report : the thirty-second report of the Steering Group on Chemical Aspects of Food Surveillance. H.M.S.O., 1992.

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Food, Steering Group on Food Surveillance Working Party on Nitrate and Related Compounds in. Nitrate, nitrite and n-nitroso compounds in food: The twentieth report of the Steering Group on Food Surveillance, the Working Party on Nitrate and Related Compounds in Food. H.M.S.O., 1987.

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Patai, Saul. Chemistry of Amino, Nitroso, Nitro and Related Groups: Supplement F2. Wiley & Sons, Incorporated, John, 1996.

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Patai, Saul. Chemistry of Amino, Nitroso, Nitro and Related Groups, Supplement F2. Wiley & Sons, Incorporated, John, 2000.

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Patai, Saul. Chemistry of Amino, Nitroso, Nitro and Related Groups, Supplement F2. Wiley & Sons, Limited, John, 2009.

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Rappoport, Zvi, and Saul E. Patai. Chemistry of Amino, Nitroso, Nitro and Related Groups, Supplement F2. Wiley & Sons Australia, Limited, John, 2003.

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Patai, Saul. Part 2, The Chemistry of Amino, Nitroso, Nitro and Related Groups, Supplement F2. Wiley, 1996.

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Book chapters on the topic "Nitroso groups"

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Eisenbrand, G., and C. Janzowski. "Potential Mechanism of Action of Nitrosamines with Hydroxy, Oxo, or Carboxy Groups." In Nitrosamines and RelatedN-Nitroso Compounds. American Chemical Society, 1994. http://dx.doi.org/10.1021/bk-1994-0553.ch015.

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Yokoshima, Satoshi. "Construction of Quinoline N-Oxides and Synthesis of Aurachins A and B: Discovery, Application, and Mechanistic Insight." In Modern Natural Product Synthesis. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-97-1619-7_17.

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AbstractA method to synthesize 3-hydroxyquinoline N-oxides from ketones having a 2-nitrophenyl group at the α-position relative to the carbonyl group was developed. The substrates were easily prepared via a SNAr reaction or a Sonogashira coupling, and treatment with sodium tert-butoxide in dimethyl sulfoxide produced the corresponding quinoline N-oxides. The method was successfully applied to the total synthesis of aurachins A and B. On the basis of the quinoline N-oxide synthesis, related reactions of α-(2-nitrophenyl)ketones, including nitrone formation and photoinduced rearrangement, were also investigated. These investigations provided clues about the reaction mechanism, and the following mechanism for the quinoline N-oxide synthesis is proposed: Deprotonation of the α-position of α-(2-nitrophenyl)ketone with tert-butoxide generates an enolate, which reacts with a nitro group via single-electron transfer to form an α-hydroxyketone having a nitroso group. An intramolecular alkoxide-mediated hydride shift reduces the nitroso group, and condensation of the resultant hydroxylamine and diketone moieties produces a 3-hydroxyquinoline N-oxide.
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Rowlands, C. C., and R. D. Farley. "15.4 Anion radicals from nitro compounds." In Landolt-Börnstein - Group II Molecules and Radicals. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-45824-1_45.

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Serra, Vanda I. Vaz, Sónia M. G. Pires, Cristina M. A. Alonso, Maria G. P. M. S. Neves, Augusto C. Tomé, and José A. S. Cavaleiro. "Meso-Tetraarylporphyrins Bearing Nitro or Amino Groups: Synthetic Strategies and Reactivity Profiles." In Topics in Heterocyclic Chemistry. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/7081_2013_101.

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von Angerer, S. "Reduction of Nitro and Nitroso Groups." In Science of Synthesis Knowledge Updates KU 2011/1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-116-00426.

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Grimmett, M. R. "Reactions of Nitroso Groups." In Five-Membered Hetarenes with Two Nitrogen or Phosphorus Atoms. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-012-00635.

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Grimshaw, James. "REDUCTION OF NITRO, NITROSO, AZO AND AZOXY GROUPS." In Electrochemical Reactions and Mechanisms in Organic Chemistry. Elsevier, 2000. http://dx.doi.org/10.1016/b978-044472007-8/50011-2.

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Reissig, H. U., B. Dugovicč, and R. Zimmer. "Substitution of Other Functional Groups." 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-041-00357.

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Bräse, S., B. Lesch, and V. Zimmermann. "Reactions with All-Carbon Functional Groups." 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-041-00561.

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Jahn, U. "Cleavage of Alkyl Groups in ,-Dialkyl--nitroamines." 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-041-00406.

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Conference papers on the topic "Nitroso groups"

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Castillo, J. J., Greg J. Tamargo, and Marc Huet. "Nitro." In SIGGRAPH '19: Special Interest Group on Computer Graphics and Interactive Techniques Conference. ACM, 2019. http://dx.doi.org/10.1145/3306449.3328830.

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Cyganiak, Olga. "Nitro nation." In SIGGRAPH '15: Special Interest Group on Computer Graphics and Interactive Techniques Conference. ACM, 2015. http://dx.doi.org/10.1145/2745234.2746997.

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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 XQ = NIQ (1), NBrQ (2), IBrQ (3) and ClBrQ (4). IR and NMR spectroscopy, elemental and X-ray structure analysis were used for their characterization. Bidentate chelate coordination of one molecule of XQ through nitrogen and oxygen atoms in square planar complexes was found. These complexes represent a group of compounds in which biological activities were found and will be used for the following biological study.
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Tolstikov, Svyatoslav, Irina Obsharova, G. Romanenko, Artem Bogomyakov, and Victor Ovcharenko. "t-Bu –GROUP SUBSTITUTION for NO2–GROUP IN NITROXIDE UNDER SOFT CONDITIONS." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m775.aks-2019/296-297.

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Núñez-Quintero, Doris, and Samuel P. Hernández-Rivera. "Spectroscopic modeling of nitro group in explosives." In Defense and Security Symposium, edited by Harold H. Szu. SPIE, 2006. http://dx.doi.org/10.1117/12.666546.

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Valery, Sinditskii, Valery Serushkin, Sergey Filatov, Irina Vatsadze, Igor Dalinger, and Aleksei Sheremetevb. "AZASIDNON EXPLOSIFOR GROUP - BEHAVIOR AT THERMOLYSIS AND COMBUSTION." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2020. http://dx.doi.org/10.29003/m719.aks-2019/42-44.

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Perry, McKynzie, Aaron Hunt, and Spencer Christian. "Ground Test Development of 800lbf Nitrous Oxide-Ethane Bipropellant Engine." In AIAA Propulsion and Energy 2020 Forum. American Institute of Aeronautics and Astronautics, 2020. http://dx.doi.org/10.2514/6.2020-3789.

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Gerunov, Taras, Marina Gonokhova, Tatyana Boyko, and Vladimir Gerunov. "Pathomorphological Changes in the Organs and Tissues of Animals During Acute Intoxication with Neonicotinoids Containing Nitroso or Cyano Group." In Proceedings of the International Scientific Conference The Fifth Technological Order: Prospects for the Development and Modernization of the Russian Agro-Industrial Sector (TFTS 2019). Atlantis Press, 2020. http://dx.doi.org/10.2991/assehr.k.200113.174.

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Patterson, Joshua D., Teresa J. Bixby, Philip J. Reid, P. M. Champion, and L. D. Ziegler. "Excited- and Ground-State Reaction Dynamics of Nitrosyl Chloride in Solution." In XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482474.

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Shusterman, Jacob, Erica Lotspeich-Britt, Hugo López Peña, and Katharine Moore Tibbetts. "Ultrafast reaction dynamics of nitro-organic molecular cations." In 23RD BIENNIAL CONFERENCE OF THE APS TOPICAL GROUP ON SHOCK COMPRESSION OF CONDENSED MATTER. AIP Publishing, 2024. https://doi.org/10.1063/12.0028666.

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Reports on the topic "Nitroso groups"

1

Boyer, J. H. Nitrolysis of the CN Single Bond and Related Chemistry of Nitro and Nitroso Groups. Defense Technical Information Center, 1985. http://dx.doi.org/10.21236/ada151753.

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2

Evgeniy, Dryuchkov, Zaporotskova Irina, and Zaporotskov Pavel. Effect of boron doping on sensing properties of CNTS functionalized with nitro group. Peeref, 2023. http://dx.doi.org/10.54985/peeref.2306p8273508.

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Chepeliev, Maksym. Development of the Non-CO2 GHG Emissions Database for the GTAP 10A Data Base. GTAP Research Memoranda, 2020. http://dx.doi.org/10.21642/gtap.rm32.

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The purpose of this note is to document data sources and steps used to develop the non-CO2 greenhouse gas (GHG) emissions database for the GTAP Data Base Version 10A. Emissions are reported for three types of non-CO2 GHGs – CH4 (methane), N2O (nitrous oxide) and the group of fluorinated gases (F-gases), and cover four reference years – 2004, 2007, 2011 and 2014. FAOSTAT dataset is used for sourcing agricultural non-CO2 emissions, EDGAR v5.0 and v4.2 databases are used to source non-agricultural emissions. Each emission flow is associated with one of the four sets of emission drivers: output by industries, endowment by industries, input use by industries and consumption by households.
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