Relevant bibliographies by topics / PHENYLHYDROXYLAMINE

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Academic literature on the topic 'PHENYLHYDROXYLAMINE'

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

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Journal articles on the topic "PHENYLHYDROXYLAMINE"

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Yu, Min, Dachen Ouyang, Liqiang Wang, and You-Nian Liu. "Catalytic Reduction of Aromatic Nitro Compounds to Phenylhydroxylamine and Its Derivatives." Molecules 29, no. 18 (2024): 4353. http://dx.doi.org/10.3390/molecules29184353.

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Phenylhydroxylamine and its derivates (PHAs) are important chemical intermediates. Phenylhydroxylamines are mainly produced via the catalytic reduction of aromatic nitro compounds. However, this catalytic reduction method prefers to generate thermodynamically stable aromatic amine. Thus, designing suitable catalytic systems, especially catalysts to selectively convert aromatic nitro compounds to PHAs, has received increasing attention but remains challenging. In this review, we initially provide a brief overview of the various strategies employed for the synthesis of PHAs, focusing on reducing
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Nichols, J. W., and L. J. Weber. "Lack of myoglobin function in the isolated perfused buffalo sculpin (Enophrys bison) heart." Canadian Journal of Zoology 68, no. 5 (1990): 825–29. http://dx.doi.org/10.1139/z90-118.

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The contribution of myoglobin to cardiac performance and O2 consumption was investigated using an isolated perfused buffalo sculpin (Enophrys bison) heart preparation. Dose–response studies at ambient (150 Torr)(1 Torr = 133.322 Pa) O2 tensions were conducted as a means of selecting an oxidizing agent with high activity toward myoglobin, while minimizing the possibility of toxic side effects. Treatment with 10.0 μM phenylhydroxylamine oxidized greater than 95% of intracellular myoglobin but did not affect pulse pressure, peak dP/dt, or heart rate. The functional importance of myoglobin was inv
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3

Pei, Linjuan, Hao Tan, Meixian Liu, et al. "Hydroxyl-group-modified polymeric carbon nitride with the highly selective hydrogenation of nitrobenzene to N-phenylhydroxylamine under visible light." Green Chemistry 23, no. 10 (2021): 3612–22. http://dx.doi.org/10.1039/d1gc00325a.

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4

Endo, Yasuyuki, Kohshi Manikawa, Toru Terashima, and Koichi Shudo. "Rearrangements of O-Phenylhydroxylamine Derivatives." HETEROCYCLES 24, no. 1 (1986): 229. http://dx.doi.org/10.3987/r-1986-01-0229.

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Mohammed, Jihad Haji, and Nabaz Abdulmajeed Mohammad Salih. "Synthesis and Characterization of Some New Nitrones Derivatives and Screening their Biological Activities." Science Journal of University of Zakho 10, no. 4 (2022): 268–73. http://dx.doi.org/10.25271/sjuoz.2022.10.4.1096.

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Synthetic approached towards the synthesis of some novel nitrones derivatives have been started with reduction of nitrobenzene derivatives as starting material bearing electron withdrawing and electron donating groups to corresponding phenylhydroxylamine in presence of zinc dust as reducing agent in aqueous solution of ammonium chloride (NH4Cl). The prepared phenylhydroxylamine derivatives were reacted with different substituted benzaldehydes to give the target derivatives of nitrone. The structures of the synthesized nitrones were characterized by spectroscopic methods FT-IR, 1H-NMR and 13C N
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Jihad Haji Mohammed and Nabaz Abdulmajeed Mohammad Salih. "SYNTHESIS AND CHARACTERIZATION OF SOME NEW NITRONES DERIVATIVES AND SCREENING THEIR BIOLOGICAL ACTIVITIES." Science Journal of University of Zakho 11, no. 2 (2023): 160–69. http://dx.doi.org/10.25271/sjuoz.2023.11.2.1149.

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Synthetic approached towards the synthesis of some novel nitrones derivatives have been started with reduction of nitrobenzene derivatives as starting material bearing electron withdrawing and electron donating groups to corresponding phenylhydroxylamine in presence of zinc dust as reducing agent in aqueous solution of ammonium chloride (NH4Cl). The prepared phenylhydroxylamine derivatives were reacted with different substituted benzaldehydes to give the target derivatives of nitrone. The structures of the synthesized nitrones were characterized by spectroscopic methods FT-IR, 1H-NMR and 13C N
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7

Kushch, S. D. "Nitrobenzene Hydrogenation to N-phenylhydroxylamine: a New Approach to the Selectivity." Eurasian Chemico-Technological Journal 4, no. 1 (2017): 19. http://dx.doi.org/10.18321/ectj513.

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A new approach to resolve the problem of selectivity with respect to N-phenylhydroxylamine in nitrobenzene hydrogenation is proposed. N-phenylhydroxylamine only is the final product of nitrobenzene electroreduction in aprotic media. In this case nitrobenzene reduction carries out by alternation of electrochemical (electron transfer) and chemical (species formed protonation) stages i.e. by so-called EC mechanism. Such mechanism realization in nitrobenzene hydrogenation is possible if i) a catalyst activates hydrogen as “hydrogen electrode” i.e. serves electrons source; ii) a reaction media cont
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8

Chakar, Fadi S., and Arthur J. Ragauskas. "Biobleaching chemistry of laccase-mediator systems on high-lignin-content kraft pulps." Canadian Journal of Chemistry 82, no. 2 (2004): 344–52. http://dx.doi.org/10.1139/v03-195.

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A high-lignin-content softwood kraft pulp was reacted with laccase in the presence of 1-hydroxybenzotriazole (HBT), N-acetyl-N-phenylhydroxylamine (NHA), and violuric acid (VA). The biodelignification response with violuric acid was superior to both 1-hydroxybenzotriazole and N-acetyl-N-phenylhydroxylamine. NMR analysis of residual lignins isolated before and after the biobleaching treatments revealed that the latter material was highly oxidized and that the magnitude of structural changes was most pronounced with the laccase – violuric acid biobleaching system. An increase in the content of c
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9

Das, Mrinal K., Matilal Nath, and Somnath De. "Synthesis and Ligand Exchange Reaction of Some Organotin(IV) Bis(N-arylsulphonyl-N-arylhydroxylaminates)." Zeitschrift für Naturforschung B 48, no. 2 (1993): 185–88. http://dx.doi.org/10.1515/znb-1993-0209.

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AbstractSeveral diorganotin(IV)-bis(N-arylsulphonyl-N-arylhydroxylaminates) of the general formula R2Sn[ON(R1)SO2R2]2 have been synthesized and characterized by elemental analyses and by IR and 1H NMR spectra. A representative ligand exchange reaction with N-benzoyl- N-phenylhydroxylamine has been carried out.
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10

Karwa, Shrikant L., and Rajeev A. Rajadhyaksha. "Selective catalytic hydrogenation of nitrobenzene to phenylhydroxylamine." Industrial & Engineering Chemistry Research 26, no. 9 (1987): 1746–50. http://dx.doi.org/10.1021/ie00069a005.

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Book chapters on the topic "PHENYLHYDROXYLAMINE"

1

Pernoud, L., J. P. Candy, B. Didillon, R. Jacquot, and J. M. Basset. "Selective hydrogenation of nitrobenzene in phenylhydroxylamine on silica supported platinum catalysts." In Studies in Surface Science and Catalysis. Elsevier, 2000. http://dx.doi.org/10.1016/s0167-2991(00)80771-5.

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