Relevant bibliographies by topics / Aromatic Amine N-oxides

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Academic literature on the topic 'Aromatic Amine N-oxides'

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

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Journal articles on the topic "Aromatic Amine N-oxides"

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R., K. AGARWAL. "Synthesis and Characterisation of Mercury(II) Complexes of some Aromatic Amine N-Oxides." Journal of Indian Chemical Society Vol. 65, Jun 1988 (1988): 448–49. https://doi.org/10.5281/zenodo.6303515.

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Department of Chemistry, Lajpat Rai (Post-Graduate) College, Sahibabad -201 005 <em>Manuscript received </em><em>23 October</em> <em>1986, </em><em>revised 18 March 1988, accepted 6 April 1988</em> Synthesis and Characterisation of Mercury(II) Complexes of some Aromatic Amine <em>N</em>-Oxides. &nbsp;
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2

Lynch, Daniel E., Graham Smith, Karl A. Byriel, and Colin H. L. Kennard. "[4-(N,N-Dimethylamino)phenyl]diphenylphosphine Oxide and its Partial Oxides: An Isomorphous Crystal Series." Australian Journal of Chemistry 56, no. 11 (2003): 1135. http://dx.doi.org/10.1071/ch03089.

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The title compound [4-(N,N-dimethylamino)phenyl]diphenylphosphine oxide (1) has been synthesized and its single-crystal X-ray structure determined. The structures of two ‘partial’ oxides of the parent compound, (2) and (3) (50% and 25% oxidized), isolated from the intermediate phosphine reaction product have also been determined, yielding an unusual isomorphous crystal series. An apparent P–O bond shortening with increasing oxidation is also observed across the series (1)–(3) (1.480(4), 1.351(4), 1.280(4) Å respectively) and is considered an artifact of the structure refinement. The packing in
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3

Chiericato Júnior, Glaico. "Complexes of lead(II) perchlorate and hexafluorophosphate with aromatic amine N-oxides." Eclética Química Journal 14, no. 1 (2018): 49. http://dx.doi.org/10.26850/1678-4618eqj.v14.1.1989.p49-56.

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4

Wolińska, Ewa. "Chiral oxazoline ligands with two different six-membered azaheteroaromatic rings – synthesis and application in the Cu-catalyzed nitroaldol reaction." Heterocyclic Communications 22, no. 2 (2016): 85–94. http://dx.doi.org/10.1515/hc-2016-0001.

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AbstractSynthesis and catalytic activity of chiral ligands 5,6-diphenyl-3-{3-[(4S/R)-4-R/Ar-4,5-dihydro-1,3-oxazol-2-yl]pyridin-2-yl}amino-1,2,4-triazines 2 and their analogs 3 possessing an N-oxide function in the pyridine ring are described. The pivotal step in the synthesis of ligands 2 is the Buchwald-Hartwig Pd-catalyzed cross-coupling reaction between 3-bromo-5,6-diphenyl-1,2,4-triazine (7a) and enantiopure 3-(4,5-dihydro-1,3-oxazol-2-yl)pyridin-2-amines 6a–d. Aromatic nucleophilic substitution of chlorine in 3-chloro-5,6-diphenyl-1,2,4-triazine (7b) with 3-(4,5-dihydro-1,3-oxazol-2-yl)p
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5

Siim, Bronwyn G., Kevin O. Hicks, Susan M. Pullen, Pierre L. van Zijl, William A. Denny, and William R. Wilson. "Comparison of aromatic and tertiary amine N-oxides of acridine DNA intercalators as bioreductive drugs." Biochemical Pharmacology 60, no. 7 (2000): 969–78. http://dx.doi.org/10.1016/s0006-2952(00)00420-2.

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6

Sarma, Rupam, та Jubaraj Bikash Baruah. "B···π-aromatic and C–H···B interactions in co-crystals of aromatic amine N-oxides with p-phenylenediboronic acid". Journal of Molecular Structure 920, № 1-3 (2009): 350–54. http://dx.doi.org/10.1016/j.molstruc.2008.11.028.

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7

Potmischil, Francisc, Helmut Herzog, and Joachim Buddrus. "Hydroacridines. Part 17—Stereospecific influence of the N+—O- group on1JC,C couplings in non-aromatic amine oxides." Magnetic Resonance in Chemistry 36, no. 4 (1998): 240–44. http://dx.doi.org/10.1002/(sici)1097-458x(199804)36:4<240::aid-omr260>3.0.co;2-9.

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8

KISHOR, ARORA. "Thermal Decomposition Kinetics of Thorium(IV) and Dioxouranium(VI) Complexes." Journal of Indian Chemical Society Vol. 74, Aug 1997 (1997): 589–96. https://doi.org/10.5281/zenodo.5890705.

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Department of Chemistry, Government Post-Graduate College, Morena-476 001 Thermal decomposition kinetics studies of thermal reactions are useful in&nbsp;studying parameters like free energy change (&Delta;<em>G</em>*), enthalpy change (&Delta;<em>H*</em>), activation energy (<em>E</em>*) and ultimately the entropy change (&Delta;<em>S</em>*) and pre-exponential factor (<em>A</em>) or frequency factor (<em>Z</em>). This concept was f&quot;u-st proposed somewhere In 1928. Since then so many methods and equations have been put forward for studying thermal decomposition kinetics of the reaction Pr
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9

Sarma, Rupam, та Jubaraj Bikash Baruah. "Corrigendum to “B···π-aromatic and C–H···B interactions in co-crystals of aromatic amine N-oxides with p-phenylenediboronic acid” Journal of Molecular Structure 920 (2009) 350–354". Journal of Molecular Structure 928, № 1-3 (2009): 195. http://dx.doi.org/10.1016/j.molstruc.2009.03.001.

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10

Read, RW, and WP Norris. "The Nucleophilic Substitution Reactions of 5- and 7-Chloro-4,6-dinitrobenzofurazan 1-Oxide by Aromatic Amines." Australian Journal of Chemistry 38, no. 3 (1985): 435. http://dx.doi.org/10.1071/ch9850435.

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7-Chloro-4,6-dinitrobenzofurazan 1-oxide is a powerful electrophile which reacts with a variety of primary and secondary aromatic amines, even those with deactivating substituents , to give arylamino - benzofurazan oxides under mild conditions. Tertiary aromatic amines react through carbon to give aminoarylbenzofurazan oxides. During, or as a consequence of, the substitution reactions, tautomerism occurs to give in all but one example an equilibrium mixture of 5- and 7-substituted 4,6-dinitrobenzofurazan oxides in which the latter predominates. Thus 5-chloro-4,6-dinitrobenzofurazan 1-oxide and
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Book chapters on the topic "Aromatic Amine N-oxides"

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"Reduction." In Biocatalysis in Organic Synthesis: The Retrosynthesis Approach. The Royal Society of Chemistry, 2018. http://dx.doi.org/10.1039/bk9781782625308-00073.

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This chapter covers enzyme classes that catalyse reduction reactions, including ketoreductases, enoate reductases, carboxylic acid reductases, imine reductases, amino acid dehydrogenases, opine dehydrogenases, amine dehydrogenases and nitro reductases. The chapter is divided into separate sections, each detailing the reduction of a specific functional group, including ketones, aldehydes, carboxylic acids, alkenes, imines, nitro aromatics, sulfoxides, azides, n-oxides and azo compounds. Each section begins with a review of chemical methods of carrying out each transformation, followed by a desc
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Conference papers on the topic "Aromatic Amine N-oxides"

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Soriaga, Manuel P., G. M. Berry, C. Bhardwaj, et al. "Chemisorption of Organic Molecules on Metal Electrode Surfaces." In CORROSION 1990. NACE International, 1990. https://doi.org/10.5006/c1990-90300.

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Abstract The chemisorption of various organic functional groups from aqueous solutions onto smooth single-crystal and polycrystalline electrodes, and the resistance of the resulting monolayer intermediates towards electrochemical oxidation have been studied; these investigations were motivated by the need to understand, at the atomic level, metal passivation by monolayer organic coatings. The electrodes employed were Rh, Pd, Ir, Pt, and Au whose anodic dissolution is preceded by surface-oxide formation even in highly acidic media. Resistance towards anodic oxidation can thus be associated with
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2

Ko, Weon Bae, Young Min Lee, and Byoung Eun Park. "Efficient method for the cleavage of fullerene oxides, [C70(O)n](n>=1) with several aromatic amines under ultrasonic irradiation." In International Congress on Ultrasonics. Vienna University of Technology, 2007. http://dx.doi.org/10.3728/icultrasonics.2007.vienna.1795_ko.

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You might also be interested in the extended bibliographies on the topic 'Aromatic Amine N-oxides' for particular source types:
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