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Relevant bibliographies by topics / N-substituted hydroxylamines

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Academic literature on the topic 'N-substituted hydroxylamines'

Author: Grafiati

Published: 4 June 2021

Last updated: 10 February 2022

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Journal articles on the topic "N-substituted hydroxylamines"

1

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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2

Svoboda, Jiří, and Jaroslav Paleček. "Synthesis of N-[(3-substituted phenoxy)alkyl]acetohydroxamic acids, potential inhibitors of the enzyme 5-lipoxygenase." Collection of Czechoslovak Chemical Communications 56, no. 6 (1991): 1317–32. http://dx.doi.org/10.1135/cccc19911317.

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The synthesis of the title compounds starts from methyl (3-subst. phenoxy)alkanoates II which are reduced to the corresponding aldehydes and then transformed to oximes V by reaction with hydroxylamine. Reduction with borane-pyridine complex gives the hydroxylamines VI which on diacetylation and partial deacetylation provide the hydroxamic acids VIII.

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3

Beirakhov, A. G., I. M. Orlova, E. G. Il’in, et al. "Molybdenum(VI) complexes with N-substituted hydroxylamines." Russian Journal of Inorganic Chemistry 58, no. 12 (2013): 1446–51. http://dx.doi.org/10.1134/s003602361312005x.

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4

Li, Xiaoqing, Xiangsheng Xu, Kun Chen, et al. "Substrate-Controlled Regioselective Iodooxygenation of Olefins." Synlett 29, no. 12 (2018): 1634–38. http://dx.doi.org/10.1055/s-0037-1609968.

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An unexpected regioselective I2/TBHP-mediated 1,2-iodooxygenation of alkenes with N-hydroxylamines is described. The reaction proceeds through a radical coupling mechanism or a iodonium mechanism, which is controlled by the structures of both N-hydroxylamines and alkenes, to form vicinal iodo-substituted N-alkoxyamines regioselectively. Both the iodo and alkoxyamine group of the resulting products offer rich possibilities of synthetic manipulations.

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5

Varma, Rajender S., and George W. Kabalka. "A CONVENIENT ONE-POT PREPARATION OF N-SUBSTITUTED HYDROXYLAMINES." Organic Preparations and Procedures International 17, no. 4-5 (1985): 254–56. http://dx.doi.org/10.1080/00304948509355515.

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6

Guan, Zhaobing, Manman Ding, Yao Sun, et al. "The synthesis of two long-chain N-hydroxy amino coumarin compounds and their applications in the analysis of aldehydes." RSC Advances 7, no. 32 (2017): 19707–16. http://dx.doi.org/10.1039/c7ra02177a.

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7

Guthrie, Daryl A., Nam Y. Kim, Maxime A. Siegler, Cathy D. Moore, and John P. Toscano. "Development of N-Substituted Hydroxylamines as Efficient Nitroxyl (HNO) Donors." Journal of the American Chemical Society 134, no. 4 (2012): 1962–65. http://dx.doi.org/10.1021/ja2103923.

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8

Bezhan, I. P., K. N. Zelenin, L. A. Sviridova, et al. "Synthesis of isoxazolidine derivatives from N-substituted hydroxylamines and ?,?-unsaturated ketones." Chemistry of Heterocyclic Compounds 25, no. 6 (1989): 684–87. http://dx.doi.org/10.1007/bf00470030.

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9

Nikitin, Kirill V., and Nonna P. Andryukhova. "Cleavage of the N–O bond in substituted hydroxylamines under basic conditions." Mendeleev Communications 10, no. 1 (2000): 32–33. http://dx.doi.org/10.1070/mc2000v010n01abeh001206.

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10

Nagakubo, Hiroshi, Gou Kubota, Kanji Kubo, Tsuyoshi Kaneko, Tadamitsu Sakurai, and Hiroyasu Inoue. "Self-Sensitized Photolysis ofN-(1-Naphthoyl)-N-phenyl-O-(benzoyl-substituted benzoyl)hydroxylamines." Bulletin of the Chemical Society of Japan 69, no. 9 (1996): 2603–11. http://dx.doi.org/10.1246/bcsj.69.2603.

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Book chapters on the topic "N-substituted hydroxylamines"

1

Cordero, F. M., and S. Cicchi. "Condensation of N-Substituted Hydroxylamines with N-Aryl-Substituted Imidates." In Three Carbon-Heteroatom Bonds: Amides and Derivatives; Peptides; Lactams. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-022-00395.

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2

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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3

Cordero, F. M., and S. Cicchi. "Reaction of N-Substituted Hydroxylamines with Alkyl Cyanoformates." In Three Carbon-Heteroatom Bonds: Amides and Derivatives; Peptides; Lactams. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-022-00400.

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