Relevant bibliographies by topics / O-hydroxylamines

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters

Academic literature on the topic 'O-hydroxylamines'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "O-hydroxylamines"

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Khomutov, R. M., and A. R. Khomutov. "Mercurated o-substituted hydroxylamines." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 34, no. 11 (1985): 2454–55. http://dx.doi.org/10.1007/bf00956834.

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Spooren, Anita AMG, and Chris TA Evelo. "Only the glutathione dependent antioxidant enzymes are inhibited by haematotoxic hydroxylamines." Human & Experimental Toxicology 17, no. 10 (1998): 554–59. http://dx.doi.org/10.1177/096032719801701005.

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Hydroxylamine and some of its derivatives are known to cause oxidative effects both in vitro and in vivo.Inthe current study we investigated the effects of hydroxyla-mines on the enzymatic antioxidant defense system in human erythrocytes. The activity of catalase and super-oxide dismutase was not significantly influenced by any of the hydroxylamines tested. However, the activity of glutathione peroxidase (GPX) and glutathione S-transferase (GST) was strongly inhibited by hydroxylamine and its O-derivatives (O-methyl and O-ethyl hydroxylamine). GPX was also inhibited by two N-derivatives of hyd
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Johnson, Alyssa L., Nathan Duncan, and Michael D. Mosher. "O-Benzyl-N-(9-acridinyl)hydroxylamines." Arkivoc 2018, no. 4 (2018): 139–48. http://dx.doi.org/10.24820/ark.5550190.p010.472.

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Clemens, Andrea, Richard P. Kreher, and Johannes Preut. "Untersuchungen zur Chemie von Isoindolen und Isoindoleninen, XXXX. 3-Hydroximino-1-alkyl(aryl)-isoindoline und 3-Hydroxylamino-1-alkyl(aryl)-1Hisoindole - Modellverbindungen für Struktur- und Reaktivitätsuntersuchungen - / Studies on the Chemistry of Isoindoles and Isoindolenines, XXXX. 3-Hydroximino-1-alkyl(aryl)-isoindolines and 3-Hydroxylamino-1-alkyl(aryl)-1Hisoindoles - Model Compounds for Investigations of Structure and Reactivity -." Zeitschrift für Naturforschung B 51, no. 12 (1996): 1791–810. http://dx.doi.org/10.1515/znb-1996-1218.

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3-Hydroximino-isoindolines and 3-hydroxylamino-1 H-isoindoles with substituents at the five membered ring have been prepared by condensation of substituted 3-alkoxy-1 H-isoindoles with hydroxylamine and O-/N -substituted hydroxylamines. Constitution and configuration of semi-cyclic amidoximes were derived from spectroscopic investigations and deduced on the basis of orientating chemical transformations. These results have been established by a crystal structure determination of a representative 3-hydroximino-isoindoline.
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Fioravanti, Stefania, Lucio Pellacani, and Paolo A. Tardella. "O-Arylsulfonyl hydroxylamines via a decarboxylative rearrangement." Tetrahedron 65, no. 29-30 (2009): 5747–51. http://dx.doi.org/10.1016/j.tet.2009.05.016.

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Matassini, Camilla, Andrea Goti, Camilla Parmeggiani, and Francesca Cardona. "On the Oxidation of Hydroxylamines with o-Iodoxybenzoic Acid (IBX)." Synthesis 49, no. 13 (2017): 2890–900. http://dx.doi.org/10.1055/s-0036-1588457.

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o-Iodoxybenzoic acid (IBX) is confirmed as a powerful tool for the oxidation of hydroxylamines. The synthetic route is demonstrated as efficient and user friendly, and is exploited on various carbohydrate-derived N,N-disubstituted hydroxylamines (cyclic, acyclic, and functionalized ones), affording the corresponding nitrones in good yields and regioselectivity. N-Monosubstituted hydroxylamines revealed an interesting divergent behavior depending on the reaction conditions. While IBX oxidation in dimethyl sulfoxide at 45 °C furnished oximes as reported, the oxidation in dichloromethane at room
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Dhanju, Sandeep, and David Crich. "Synthesis of N,N,O-Trisubstituted Hydroxylamines by Stepwise Reduction and Substitution of O-Acyl N,N-Disubstituted Hydroxylamines." Organic Letters 18, no. 8 (2016): 1820–23. http://dx.doi.org/10.1021/acs.orglett.6b00556.

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Aurich, Hans Günter, Christian Gentes та Ulrich Sievers. "Darstellung chiraler heterocyclischer β-Aminosäureester / Preparation of Chiral Heterocyclic Esters of β-Amino Acids". Zeitschrift für Naturforschung B 54, № 4 (1999): 519–31. http://dx.doi.org/10.1515/znb-1999-0416.

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Chiral β-amino alcohols were successively prone to N-benzylation, O-allylation and oxidation of the resulting benzylamino group to give nitrones 3 which on hydrolysis afforded chiral hydroxylamines HO-NH-CH(R)-CH2-O-CH2-CH=CH2 ((S)-4: R = Me, Bn, iPr. (R)-4: R = Et). Swern oxidation of methyl 2,2-dimethyl-3-hydroxypropionate (16) and treatment of the resulting aldehyde 17 with hydroxylamines (S)-4b (R = Bn) or (R)-4d (R = Et) provided nitrones 18 that underwent an intramolecular 1,3-dipolar cycloaddition on heating yielding the bicyclic β-amino-acid esters 19b and ent-19d, respectively.Reducti
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Bates, Roderick W., and Kanicha Sa-Ei. "O-Alkenyl Hydroxylamines: A New Concept for Cyclofunctionalization." Organic Letters 4, no. 24 (2002): 4225–27. http://dx.doi.org/10.1021/ol026701d.

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Defoin, Albert, Sébastien Albrecht, and Céline Tarnus. "Simple Preparation of O-Substituted Hydroxylamines from Alcohols." Synthesis 2006, no. 10 (2006): 1635–38. http://dx.doi.org/10.1055/s-2006-926440.

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Dissertations / Theses on the topic "O-hydroxylamines"

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Milner, Harry. "The use of O-(diphenylphosphinyl)hydroxylamines and nitrogen-selenium ylides in transition-metal-free aminations of sp2 carbon centres." Thesis, Imperial College London, 2015. http://hdl.handle.net/10044/1/25510.

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Due to their abundance in both natural products and synthetic pharmaceuticals, and their diverse and interesting biological properties, nitrogen containing compounds are of great importance to organic chemists. As such, synthetic methodology for the incorporation of nitrogen into organic compounds via the construction of C-N bonds is highly sought after. The research described in this thesis concerns the development of three methodologies for the synthesis of small nitrogen containing compounds via the amination of carbon sp2 centres: 1) Synthesis of N-Boc-aziridines Building upon recent repor
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Wang, Yue-Ting. "Detection of reactive intermediates from quinol esters and O-aryl-N-methanesulfonyl hydroxylamine." Miami University / OhioLINK, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=miami1249001098.

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Labarthe, Émilie. "Nouvelle stratégie d'élaboration de la N-aminopipéridine via l'acide hydroxylamine-O-sulfonique : synthèse, modélisation cinétique, équilibres entre phases, extraction et procédés." Lyon 1, 2008. http://www.theses.fr/2008LYO10319.

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Luke, April M. Swenberg James A. Nakamura Jun. "An O-hydroxylamine-coupled alkaline gel electrophoresis assay demonstrates an accumulation of real single strand breaks and intact AP sites in base excision repair deficient cells." Chapel Hill, N.C. : University of North Carolina at Chapel Hill, 2009. http://dc.lib.unc.edu/u?/etd,2429.

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Thesis (M.S.)--University of North Carolina at Chapel Hill, 2009.<br>Title from electronic title page (viewed Sep. 3, 2009). "... in partial fulfillment of the requirements for the degree of Master of Science in the Curriculum in Toxicology." Discipline: Toxicology; Department/School: Medicine.
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Talan, Rommel S. "Chemical Ligation of Glycopeptides." University of Toledo / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1278958947.

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You, Zun-Hui, and 尤俊輝. "O-(2,3,4,5,6-pentafluorobenzyl) hydroxylamine hydrochloride as a sensitive derivatizing agent for the diffusive sampler of formaldehyde." Thesis, 1994. http://ndltd.ncl.edu.tw/handle/83749098492428769083.

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Books on the topic "O-hydroxylamines"

1

Al-Ubaidi, A. K. W. A study of the reactions of hydroxylamine-o-sulphonic acid. 1985.

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Book chapters on the topic "O-hydroxylamines"

1

Schmidt, C., R. Schmidt, and H. U. Demuth. "Elastases and subtilisins: Inactivation with N-peptidyl-O-aroyl hydroxylamines." In Peptides 1990. Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-3034-9_316.

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Matsuguma, Harold J., Ludwig F. Audrieth, and H. L. Wehrmeister. "Hydroxylamine-O -Sulfonic Acid." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132364.ch32.

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Schomburg, Dietmar, and Dörte Stephan. "Aromatic-hydroxylamine O-acetyltransferase." In Enzyme Handbook 11. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-61030-1_188.

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Luke, April M., and Jun Nakamura. "O-Hydroxylamine-Coupled Alkaline Gel Electrophoresis Assay for the Detection and Measurement of DNA Single-Strand Breaks." In Methods in Molecular Biology. Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-998-3_21.

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Ostrowska, K., and A. Kolasa. "Reactions of Imidoyl Chlorides with Hydroxylamine, O-Substituted, or N-Substituted Hydroxylamines." In Three Carbon-Heteroatom Bonds: Amides and Derivatives; Peptides; Lactams. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-022-00580.

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"Synthesis of O-(6-Deoxy-α- and β-l-Galactopyranosyl) Hydroxylamines (α- and β-l-Fucopyranosyl hydroxylamines)." In Carbohydrate Chemistry. CRC Press, 2016. http://dx.doi.org/10.1201/b11261-48.

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KHOMUTOV, A. R., R. M. KHOMUTOV, T. O. ELORANTA, L. PERSSON, C. W. PORTER, and V. G. DZAVAKHIA. "Chemical Regulation of Polyamine Biosynthesis in Cell Cultures by Polyfunctional O-Substituted Hydroxylamines." In Enzymes Dependent on Pyridoxal Phosphate and Other Carbonyl Compounds As Cofactors. Elsevier, 1991. http://dx.doi.org/10.1016/b978-0-08-040820-0.50117-5.

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Merino, P. "From Hydroxylamines." In Acetals: Hal/X and O/O, S, Se, Te. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-029-00654.

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Sartori, G., and R. Maggi. "Addition of Hydroxylamines to Electron-Deficient Allenes." In X-Ene-X (X=F, Cl, Br, I, O, S, Se, Te, N, P), Ene-Hal, and Ene-O Compounds. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-032-00754.

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"__MPSCONT__2. aus anderen O-(l-Alkenyl)-hydroxylaminen." In En,X- und In,X-Verbindungen, edited by Heinz Kropf and Ernst Schaumann. Georg Thieme Verlag, 1993. http://dx.doi.org/10.1055/b-0035-112099.

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