Relevant bibliographies by topics / Nitrosobenzene

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

Academic literature on the topic 'Nitrosobenzene'

Author: Grafiati
Published: 4 June 2021
Last updated: 17 February 2022

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Journal articles on the topic "Nitrosobenzene"

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De, Surya K., Mrinal G. Dhara, and Asok K. Mallik. "Synthesis of trans-2,3-dimethoxy-3- (phenylamino)flavanones and related compounds." Canadian Journal of Chemistry 76, no. 2 (1998): 199–204. http://dx.doi.org/10.1139/v97-219.

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trans-2,3-Dimethoxy-3-(phenylamino)flavanones (2), a new type of flavanone derivatives, are synthesized from flavanones or 2'-hydroxychalcones in two steps, the first one being a condensation with nitrosobenzenes (Ehrlich-Sachs reaction) and the second an oxidation with (diacetoxyiodo)benzene in methanol. Nitrone formation, an important side reaction of the Ehrlich-Sachs reaction, has also been exploited to synthesize 2 simply by use of an excess of nitrosobenzene in aqueous methanol. Syntheses of several analogues of 2 are also reported.Key words: trans-2,3-dimethoxy-3-(phenylamino)flavanones
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da Machado, Fernanda. "Nitrosobenzene." Synlett 2008, no. 19 (2008): 3075–76. http://dx.doi.org/10.1055/s-2008-1067280.

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CROSTON, M., J. LANGSTON, G. TAKACS, et al. "CONVERSION OF ANILINE TO AZOBENZENE AT FUNCTIONALIZED CARBON NANOTUBES: A POSSIBLE CASE OF A NANODIMENSIONAL REACTION." International Journal of Nanoscience 01, no. 03n04 (2002): 285–93. http://dx.doi.org/10.1142/s0219581x02000255.

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Aniline is oxidized to nitrosobenzene as the initial product, which undergoes further oxidation to nitrobenzene. The nitrosobenzene formation is catalyzed by functionalized multiwalled carbon nanotubes (CNT) followed by a coupling reaction between nitrosobenzene and aniline to produce azobenzene. This coupling requires close proximity of the reactants. It proceeds rapidly resulting in the UV-VIS absorption spectrum showing maxima at 327 nm and 425 nm. The nitrosobenzene yield in the presence of CNTs is controlled by the amount present in the medium. As the reaction is not catalyzed by unfuncti
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Brook, Adrian G., and Abraha Habtemariam. "Insertion reactions of nitrosobenzene and ketenes into silaaziridines." Canadian Journal of Chemistry 81, no. 11 (2003): 1164–67. http://dx.doi.org/10.1139/v03-001.

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Nitrosobenzene, trimethylsilyl ketene, and diphenylketene insert into the ring of silaaziridines to yield relatively unstable 5-membered heterocyclic ring systems. The new compounds, which have been characterized by 1H, 13C, and 29Si NMR spectroscopy, arise from two different modes of insertion into the ring Si—N bond, leading to compounds with an exocyclic C=N bond (from nitrosobenzene) or two exocyclic C=C bonds (from the ketenes).Key words: silaaziridines, ring insertion, nitrosobenzene, ketenes, heterocyclic rings.
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Bubnov, Yurii N., Dmitrii G. Pershin, Anna L. Karionova, and Mikhail E. Gurskii. "Allylboration of nitrosobenzene." Mendeleev Communications 12, no. 5 (2002): 202–3. http://dx.doi.org/10.1070/mc2002v012n05abeh001640.

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Niles, Stanley, and Charles A. Wight. "Photofragment spectroscopy of nitrosobenzene." Chemical Physics Letters 154, no. 5 (1989): 458–62. http://dx.doi.org/10.1016/0009-2614(89)87131-3.

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Matsuo, Jun-ichi, Yusuke Shima, Emiko Igarashi, and Tomoyuki Yoshimura. "Reactions of Nitrosobenzenes with Cyclobutanones by Activation with a Lewis Acid." Synlett 29, no. 06 (2017): 723–26. http://dx.doi.org/10.1055/s-0036-1588469.

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Formal [4+2] cycloaddition between 3-ethoxy-2-alkylcyclobutanones and nitrosobenzene proceeded by activation with Me3SiOTf to afford 6-alkyl-2-phenyl-2H-1,2-oxazin-5(6H)-one by regioselective cleavage of the more substituted C2–C3 bond of the cyclobutanone ring. On the other hand, reactions of 3-phenylcyclobutanones and 2-benzyloxycyclobutanone with nitrosobenzene gave γ,δ-unsaturated and cyclic hydroxamic acid derivatives, respectively, by cleavage of a cyclobutanone C1–C2 bond.
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Packett, Diane L., William C. Trogler, and Arnold L. Rheingold. "Molecular structure of (.mu.-.eta.1-nitrosobenzene-N)(.mu.-.eta.2-nitrosobenzene-N,O)(.eta.1-nitrosobenzene-N)tris(trimethylphosphine)diplatinum(II), a complex containing three linkage isomers of nitrosobenzene." Inorganic Chemistry 26, no. 26 (1987): 4308–9. http://dx.doi.org/10.1021/ic00273a006.

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He, Jing Hui, Wei Mao, Wei Chen, Kai Wu, Han Song Cheng, and Guo Qin Xu. "Resolving molecular orbitals self-decoupled from semiconductor surfaces." Chem. Sci. 5, no. 11 (2014): 4447–52. http://dx.doi.org/10.1039/c4sc01293c.

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Li, Huanhuan, Can Huang, Yingying Li, Weijun Yang, and Fan Liu. "Electrocatalytic reduction of trace nitrobenzene using a graphene-oxide@polymerized-manganese-porphyrin composite." RSC Advances 9, no. 39 (2019): 22523–30. http://dx.doi.org/10.1039/c9ra02932j.

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Dissertations / Theses on the topic "Nitrosobenzene"

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Kyne, Robert E. "Strategic Applications of Pinacolato Allylboron Reagents: New Reactions in Enantioselective Allyl-Allyl Cross-Coupling and Allylboration to Form New Carbon-Heteroatom Bonds." Thesis, Boston College, 2012. http://hdl.handle.net/2345/3163.

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Thesis advisor: James P. Morken<br>Detailed within this dissertation are three new reactions involving allylboron reagents. Chapter 1 describes the development of Pd-catalyzed allyl-allyl cross-coupling for the preparation of enantioenriched all-carbon quaternary stereogenic centers. This methodology represents a novel approach to a significant challenge for synthetic chemists. Subsequently, an allyl-allyl cross-coupling is described which generates functionally differentiated 1,5-dienes. Such structures allow for several chemoselective manipulations, which add a significant practical note to
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Ferretti, Eleonora. "Reductive Activation of Nitric Oxide and Nitrosobenzene at a Dinickel(II) Dihydride Complex and New Pyrazole-Based Diiron Compounds." Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2018. http://hdl.handle.net/11858/00-1735-0000-002E-E594-D.

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Ferretti, Eleonora [Verfasser], Franc [Akademischer Betreuer] Meyer, Franc [Gutachter] Meyer, and Inke [Gutachter] Siewert. "Reductive Activation of Nitric Oxide and Nitrosobenzene at a Dinickel(II) Dihydride Complex and New Pyrazole-Based Diiron Compounds / Eleonora Ferretti ; Gutachter: Franc Meyer, Inke Siewert ; Betreuer: Franc Meyer." Göttingen : Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2019. http://d-nb.info/1195215851/34.

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Fletcher, Daniel Allen. "Structural studies of aromatic C-Nitroso compounds using NMR techniques." Thesis, University of Exeter, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.307275.

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Lynch, Peter Neil. "An investigation into the reactivity of nitrosobenzenes as carcinogenic metabolites of nitrobenzenes and anilines." Thesis, University of Newcastle Upon Tyne, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.361594.

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GUILBAUD-CRIQUI, ANNE. "Electrosynthese, sur electrodes poreuses, de nitrosobenzenes o-substitues. Etude de leur reactivite dans le milieu d'electrolyse." Rennes 1, 1992. http://www.theses.fr/1992REN10118.

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Des nitrosobenzenes substitues en position ortho par des fonctions carboxylique (a), ester (b), amide (c), acetique (d), hydroxyacetique (e), carbamate (f) et sulfonamide (g) ont ete prepares, a partir des composes nitres correspondants, dans une cellule d'electrolyse redox a circulation equipee de deux electrodes poreuses consecutives de polarites opposees. L'addition d'acides sulfiniques aux derives nitroses fournit des phenylhydroxylamines n-sulfonylees qui, pour les series (a), (b), et (c), se cyclisent en benzisoxazolones n-sulfonylees. Aucune cyclisation n'a ete observee pour les autres
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Lamoureux, Catherine. "Mise au point et controle du fonctionnement de cellules d'electrolyse de type redox : application a la synthese de nitrosobenzenes." Rennes 1, 1986. http://www.theses.fr/1986REN10061.

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Donnees sur les cellules "redox" ou la solution circule a travers une electrode bipolaire poreuse ou 2 electrodes consecutives et de polarites inverses, mises au point pour effectuer, a la suite l'une de l'autre, 2 reactions electrochimiques opposees (reduction puis oxydation ou inversement). Les exemples choisis pour le controle du fonctionnement de telles cellules concernent la preparation de derives nitroses a partir de nitrobenzenes : la phenylhydroxylamine, formee par reduction dans la premiere partie de l'ensemble poreux est ensuite oxydee en nitrobenzene dans la deuxieme partie
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Lamoureux, Catherine. "Mise au point et contrôle du fonctionnement de cellules d'électrolyse de type Redox application à la synthèse de nitrosobenzènes." Grenoble 2 : ANRT, 1986. http://catalogue.bnf.fr/ark:/12148/cb375989234.

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Chen, Jing, and 陳敬. "Reductive Dimerization of Nitrosobenzene Compounds: Synthesis of Dissymmetrical Azoxybenzenes." Thesis, 2016. http://ndltd.ncl.edu.tw/handle/73542478728336740252.

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碩士<br>中原大學<br>化學研究所<br>104<br>An azoxybenzene compounds are synthesized using different notrosobenzene compounds under mild conditions. It further shows the production of symmetrical and dissymmetrical azoxybenzene compounds. The obtained products are successfully identified and characterized using NMR (1H and 13C), IR, MS and Xray.
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Chen, Ching Lin, and 陳敬霖. "Metal-Free Radical Addition to Diketone via Propenone with Alkene and Cycloaddition of Dienylbenzene and Nitrosobenzene to Isoxazole Derivatives." Thesis, 2016. http://ndltd.ncl.edu.tw/handle/8qd63x.

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碩士<br>國立清華大學<br>化學系<br>105<br>PART 1 Here, we described the synthesis of 2-substituted-3-oxo-N-phenylbutanamide through an efficient radical addition reaction. Optimizing the condition for the radical addition of alkenes with (E)-4-(phenylamino)-4-((2,2,6,6-tetramethylpiperidin-1-yl)oxy) prop-3-en-1-substituted-2-one, and we have it best performed at 120 oC in toluene that described with moderate to good yields. The structures of products consist of diketone and N-phenylamide, which could be used for further applications such as providing starting materials for Mannich reaction to synthesize n
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Book chapters on the topic "Nitrosobenzene"

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Mukherjee, S. "α-Hydroxyamination Using Nitrosobenzene." In Lewis Base and Acid Catalysts. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-204-00086.

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Mukherjee, S. "α-Aminoxylation Using Nitrosobenzene." In Lewis Base and Acid Catalysts. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-204-00090.

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MacMillan, D. W. C., and A. J. B. Watson. "α-Oxidation Reactions Using Nitrosobenzene." In Stereoselective Pericyclic Reactions, Cross Coupling, and C—H and C—X Activation. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-203-00440.

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MacMillan, D. W. C., and A. J. B. Watson. "α-Amination Reactions Using Nitrosobenzene." In Stereoselective Pericyclic Reactions, Cross Coupling, and C—H and C—X Activation. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-203-00445.

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Smith, Gerard V., Ruozhi Song, Gasior Marian, and Russell E. Malz. "Hydrogenation of Nitrosobenzene over Palladium Catalysts." In Catalysis of Organic Reactions. CRC Press, 2020. http://dx.doi.org/10.1201/9781003067184-11.

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Gallagher, P. T. "Reaction between Benzyne and a Nitrosobenzene." In Fused Five-Membered Hetarenes with One Heteroatom. Georg Thieme Verlag KG, 2001. http://dx.doi.org/10.1055/sos-sd-010-00872.

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Rossi, L. "Palladium-Catalyzed Reductive Carbonylation of Nitrosobenzene." In Four Carbon-Heteroatom Bonds. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-018-00662.

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Cordero, F. M., and S. Cicchi. "Reaction of Thiazolidin-4-ones with Nitrosobenzene." In Three Carbon-Heteroatom Bonds: Amides and Derivatives; Peptides; Lactams. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-022-00380.

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"Competitive Hydrogenation of Nitrobenzene, Nitrosobenzene and Azobenzene." In Catalysis of Organic Reactions. CRC Press, 2006. http://dx.doi.org/10.1201/9781420007794-29.

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Jackson, S., Elaine Gelder, and C. Martin Lok. "Competitive Hydrogenation of Nitrobenzene, Nitrosobenzene and Azobenzene." In Catalysis of Organic Reactions. CRC Press, 2006. http://dx.doi.org/10.1201/9781420007794.ch20.

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