Relevant bibliographies by topics / Nitrobenzoyl

Contents

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

Academic literature on the topic 'Nitrobenzoyl'

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

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Journal articles on the topic "Nitrobenzoyl"

1

Park, Kyoung-Ho, Chan Joo Rhu, Jin Burm Kyong, and Dennis N. Kevill. "The Effect of the ortho Nitro Group in the Solvolysis of Benzyl and Benzoyl Halides." International Journal of Molecular Sciences 20, no. 16 (2019): 4026. http://dx.doi.org/10.3390/ijms20164026.

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A kinetic study was carried out on the solvolysis of o-nitrobenzyl bromide (o-isomer, 1) and p-nitrobenzyl bromide (p-isomer, 3), and o-nitrobenzoyl chloride (o-isomer, 2) in a wide range of solvents under various temperatures. In all of the solvents without aqueous fluoroalcohol, the reactions of 1 were solvolyzed at a similar rate to those observed for 3, and the reaction rates of 2 were about ten times slower than those of the previously studied p-nitrobenzoyl chloride (p-isomer, 4). For solvolysis in aqueous fluoroalcohol, the reactivity of 2 was kinetically more reactive than 4. The l/m v
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Białońska, Agata, and Zbigniew Ciunik. "Hydrophobic `lock and key' recognition of N-4-nitrobenzoylamino acid by strychnine." Acta Crystallographica Section B Structural Science 62, no. 6 (2006): 1061–70. http://dx.doi.org/10.1107/s0108768106025249.

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During racemic resolution of N-4-nitrobenzoyl-DL-amino acids (alanine, serine and aspartic acid) by a fractional crystallization of strychninium salts, crystals of both diastereomeric salts were grown, and the crystal structures of strychninium N-4-nitrobenzoyl-L-alaninate methanol disolvate (1a), strychninium N-4-nitrobenzoyl-D-alaninate dihydrate (1b), strychninium N-4-nitrobenzoyl-D-serinate dihydrate (2a), strychninium N-4-nitrobenzoyl-L-serinate methanol solvate hydrate (2b), strychninium hydrogen N-4-nitrobenzoyl-L-aspartate 3.75 hydrate (3a) and strychninium hydrogen N-4-nitrobenzoyl-D-
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MANAP, Sevda, Haydar YÜKSEK, Zeynep EKİNCİ, and Elif SEL. "In vitro Antioxidant and Antimicrobial Activities of Some Novel 3-Alkyl-4-[3-methoxy-4-(p-nitrobenzoxy)-benzylideneamino]-4,5-dihydro-1H-1,2,4-triazol-5-ones." Afyon Kocatepe University Journal of Sciences and Engineering 22, no. 2 (2022): 275–81. http://dx.doi.org/10.35414/akufemubid.1008079.

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In this study, nine novel 3-alkyl-4-[3-methoxy-4-(p-nitrobenzoxy)-benzylideneamino]-4,5-dihydro-1H-1,2,4-triazol-5-ones (3) were synthesized from the reactions of 3-alkyl-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones (1) with 3-methoxy-4-(p-nitrobenzoxy)-benzaldehyde (2), which was synthesized by the reaction of 3-methoxy-4-hydroxybenzaldehyde with p-nitrobenzoyl chloride by using triethylamine. The structures of novel compounds were established from IR, 1H NMR and 13C NMR spectral data. In addition, in vitro antibacterial capacities of the new compounds were determined against six bacteria by m
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Lipin, D. V., E. I. Denisova, D. A. Shipilovskikh, R. R. Makhmudov, N. M. Igidov, and S. A. Shipilovskikh. "Decyclization of substituted 3-(4-nitrobenzoyl)hydrasono3<i>H</i>-furan-2-ones under the action of primary alcohols and investigation of analgesic activity and acute toxicity of reaction products." Журнал органической химии 59, no. 4 (2023): 516–24. http://dx.doi.org/10.31857/s0514749223040109.

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The decyclization of substituted 3-(4-nitrobenzoyl)hydrazono-3 H -furan-2-ones under the action of primary alcohols, which proceeds with the formation of the corresponding substituted 2-[2-(4-nitrobenzoyl)hydrazono]-4-oxobutanoates, has been studied. The analgesic activity and acute toxicity of the obtained compounds were studied, it was found that the obtained compounds exhibit a pronounced analgesic effect, and also have low toxicity. According to the drug toxicity classification, the obtained primary substituted 2-[2-(4-nitrobenzoyl)hydrazono]-4-oxobutanoates belong to class V of practicall
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Yang, Sen-Lin, and Zhi-Gang Luo. "N′-(2-Nitrobenzoyl)benzohydrazide." Acta Crystallographica Section E Structure Reports Online 63, no. 7 (2007): o3208. http://dx.doi.org/10.1107/s1600536807028024.

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Suchetan, P. A., Sabine Foro, and B. Thimme Gowda. "N-(3-Nitrobenzoyl)benzenesulfonamide." Acta Crystallographica Section E Structure Reports Online 68, no. 5 (2012): o1507. http://dx.doi.org/10.1107/s1600536812016765.

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Saeed, Aamer, and Michael Bolte. "1-(4-Nitrobenzoyl)-3-phenylthiourea." Acta Crystallographica Section E Structure Reports Online 63, no. 8 (2007): o3553. http://dx.doi.org/10.1107/s1600536807034587.

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Jiang, Xue-Yue, Xiao-Jun Feng, Song Yang, Hua-Jie Xu, and Ling-Yun Hao. "1,2-Bis(4-nitrobenzoyl)hydrazine." Acta Crystallographica Section E Structure Reports Online 65, no. 9 (2009): o2189. http://dx.doi.org/10.1107/s160053680903181x.

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Woelfle, Ingrid, Björn Sauerwein, Tom Autrey, and Gary B. Schuster. "THE PHOTOCHEMISTRY OF 3-NITROBENZOYL AND 4-NITROBENZOYL AZIDES: POSSIBLE REAGENTS FOR PHOTOAFFINITY LABELING." Photochemistry and Photobiology 47, no. 4 (1988): 497–501. http://dx.doi.org/10.1111/j.1751-1097.1988.tb08837.x.

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Fang, Wei, Xiuping Lin, Xuefeng Zhou, et al. "Cytotoxic and antiviral nitrobenzoyl sesquiterpenoids from the marine-derived fungus Aspergillus ochraceus Jcma1F17." Med. Chem. Commun. 5, no. 6 (2014): 701–5. http://dx.doi.org/10.1039/c3md00371j.

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Dissertations / Theses on the topic "Nitrobenzoyl"

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Hossli, Stefan. "Ueber die Chlorodenitrierung von 1,2-Dimethyl-3-Nitrobenzol /." Zürich, 1994. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=10782.

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Globisch, Stefan. "Systematische Untersuchungen zur Photochemie der o-Nitrobenzyl- Schutzgruppe." [S.l. : s.n.], 2002. http://deposit.ddb.de/cgi-bin/dokserv?idn=965859169.

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Since, Marc. "Stratégie TDAE : outils synthétiques et applications pharmacochimique." Thesis, Aix-Marseille 2, 2011. http://www.theses.fr/2011AIX22953.

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Ce travail est consacré au développement de la stratégie TDAE dans le cadre de la synthèse de nouveaux composés à visée thérapeutique. Dans une première partie, la pharmacomodulation d’un composé potentiellement ligand sélectif du récepteur 5-HT7 nous a conduit à développer une méthodologie d’addition et d’estérification séquentielle « one-pot » initiée par le TDAE. Par la suite, nous avons étendu la réactivité initiée par le TDAE aux réactions de substitution nucléophile de type 2 sur des électrophiles &#61537;-halogénoesters et &#61537;-halogénoamides en série nitrobenzylique. Cette méthodol
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Since, Marc. "Stratégie TDAE : outils synthétiques et applications pharmacochimique." Electronic Thesis or Diss., Aix-Marseille 2, 2011. http://www.theses.fr/2011AIX22953.

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Ce travail est consacré au développement de la stratégie TDAE dans le cadre de la synthèse de nouveaux composés à visée thérapeutique. Dans une première partie, la pharmacomodulation d’un composé potentiellement ligand sélectif du récepteur 5-HT7 nous a conduit à développer une méthodologie d’addition et d’estérification séquentielle « one-pot » initiée par le TDAE. Par la suite, nous avons étendu la réactivité initiée par le TDAE aux réactions de substitution nucléophile de type 2 sur des électrophiles &#61537;-halogénoesters et &#61537;-halogénoamides en série nitrobenzylique. Cette méthodol
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Bonacker, Daniela. "Gentoxizität und Zytotoxizität von Substanzen, die das Zytoskelett beeinflussen (Blei, Quecksilber, Nitrobenzol, Benzonitril)." [S.l.] : [s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=972224998.

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Schaal, Janina. "Synthese und Photochemie von photoaktivierbaren Biomolekülen." Phd thesis, Universität Potsdam, 2011. http://opus.kobv.de/ubp/volltexte/2012/5792/.

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Mechanistische und kinetische Untersuchungen von komplexen zellulären Prozessen in situ sind in den vergangenen Jahren durch den Einsatz photoaktivierbarer Biomoleküle, sogenannter caged Verbindungen, möglich geworden. Bei den caged Verbindungen handelt es sich um photolabile inaktive Derivate von biologisch aktiven Molekülen, aus denen durch ultraviolettes Licht mit Hilfe einer photochemischen Reaktion die natürliche, biologisch aktive Substanz schnell freigesetzt werden kann. Im Rahmen der vorliegenden Arbeit wurden caged Verbindungen von den Neurotransmittern Octopamin und Dopamin, dem Octo
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Cheibani, Ismail. "Formation et clivage de gels de nanoparticules lipidiques : systèmes de délivrance de principes actifs." Thesis, Université Grenoble Alpes (ComUE), 2016. http://www.theses.fr/2016GREAV017/document.

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Les nanotechnologies sont devenues depuis plusieurs années un axe majeur de développement dans les domaines du diagnostic, de l’imagerie, de la délivrance de médicament, du suivi thérapeutique et de l’ingénierie tissulaire. L’administration de produits non injectables sous leur forme libre ou bien possédant une toxicité élevée, peut être facilitée par l’utilisation de nanovecteurs, modifiant leur distribution. Ils permettent donc de réduire les doses administrées, limiter les effets secondaires et diriger le contenu du vecteur (agent de contraste, drogue) vers un organe cible ou une tumeur, en
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Kevwitch, Robert M. "Strategies for degradable dendrimers: Fragmenting o-nitrobenzyl ether dendrimers and disassembling oligomers of model dendritic systems." Diss., The University of Arizona, 2004. http://hdl.handle.net/10150/280481.

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Two dendrimer cores that contain o-nitrobenzyl photolabile moieties have been synthesized from piperonal. Methylated core analogs undergo clean photocleavage as indicated by the evolution of isosbestic points in the UV spectra during photolysis and the observation of degradation products by ¹H NMR. These dendrimer cores serve as precursors to dendrimer-based photodegradable materials. Second generation benzyl aryl ether dendrimers have been synthesized and undergo clean photocleavage as indicated by the evolution of isosbestic points in the UV spectra during photolysis and the observation of d
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Guo, Xi. "The development and applications of unsymmetrical diboron compounds." Diss., Virginia Tech, 2014. http://hdl.handle.net/10919/71393.

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Organoboron compounds have shown a wide variety of applications in both organic synthesis and the pharmaceutical field in the past decades. Transition metal-catalyzed boration of unsaturated compounds has been studied extensively as an efficient method to install C-B bonds. Most of the previous examples employed symmetrical diboron reagents such as B₂(pin)₂ (pin = pinacolate) and B₂(cat)₂ (cat = catecholate). There are, however, limited examples of boration using unsymmetrical diboron reagents. This dissertation discloses two transition metal-catalyzed borations of unsaturated compounds with u
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Soliman, Soliman Mehawed Abdellatif. "From photosensitive glycopolymers to smart drug delivery systems." Thesis, Université de Lorraine, 2014. http://www.theses.fr/2014LORR0147/document.

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Des glycopolymères greffés et dibloc, amphiphiles et photosensibles, à base de poly(acrylate d'o-nitrobenzyle) (PNBA) hydrophobe et photoclivable et de dextrane hydrophile ont été préparés avec succès en utilisant notammennt une réaction d'Huisgen (Cycloaddition Azoture-Alcyne catalysée par le Cuivre (I) - CuAAC chimie click). Dans un premier temps, la polymérisation de l'acrylate d'o-nitrobenzyle a été contrôlée avec succès grâce aux développements récents de la polymérisation radicalaire vivante par transfert d'un seul électron (SET-LRP). Nous avons alors obtenu un PNBA fonctionnalisé à son
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Books on the topic "Nitrobenzoyl"

1

Gesellschaft Deutscher Chemiker. Beratergremium für Umweltrelevante Altstoffe., ed. 1,4-Dichlor-2-nitrobenzol. VCH, 1992.

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Gutenberg-Universität, Johannes, ed. Untersuchungen zur Umsetzung von N-Butylamin mit 2-(2-Hydroxy-5-Nitrobenzyl)-4-Methylphenylacetat und geeigneten Modellverbindungen. [s.n.], 1988.

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Osborne, Craig. Measuring the rate constant and secondary a-deuterium kinetic isotope effect for the SN2 reaction between para-nitrobenzyl choride and cyanide ion in 15% aqueous DMSO. Laurentian University, 1996.

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National Toxicology Program (U.S.). NTP technical report on the toxicology and carcinogenesis studies of p-nitrobenzoic acid (CAS no. 62-23-7) in F344/N rats and B6C3F́ mice: Feed studies. U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, 1994.

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L, Davies, WHO Task Group on Environmental Health Criteria for Nitrobenzene., United Nations Environment Programme, et al., eds. Nitrobenzene. World Health Organization, 2003.

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2-Nitrophenol : (2-Hydroxy-nitrobenzol). 4-Nitrophenol: (4-Hydroxy-nitrobenzol). VCH Verlagsgesellschaft mbH, 1992.

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1,4-Dichlor-2-nitrobenzol. VCH Verlagsgesellschaft mbH, 1992.

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Matter, Walter. 1-Nitroanthrachinon aus 1,2-Dimerhyl-3-Nitrobenzol. 1987.

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Hossli, Stefan. Über die Chlorodenitrierung von 1,2-Dimethyl-3-Nitrobenzol. 1994.

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Haase, Rolf. Thermodiffusion Im Kritischen Entmischungsgebiet des Flüssigen Systems Nitrobenzol + N-Hexan. VS Verlag fur Sozialwissenschaften GmbH, 2013.

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Book chapters on the topic "Nitrobenzoyl"

1

Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with 1,4,8,11-tetra(2-nitrobenzoyl)-1,4,8,11-tetraazacyclotetradecane." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 8. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-66460-5_392.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with 1,4,8,11-tetra(4-nitrobenzoyl)-1,4,8,11-tetraazacyclotetradecane." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 8. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-66460-5_391.

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Holze, Rudolf. "Ionic conductance of o-nitrobenzoic acid." In Electrochemistry. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_523.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of dicopper(II) complex with 2-nitrobenzoic acid." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 4. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62474-6_217.

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Pardasani, R. T., and P. Pardasani. "Molar magnetic susceptibility of 1-(4′-nitrobenzyl)pyridinium bis(maleonitriledithiolato)iron(III)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 1. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62478-4_437.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand coper(II) complex with p-nitrobenzoic acid and pyridine-N-oxide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 6. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65056-1_368.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of polymeric mixed ligand manganese(II) complex with p-nitrobenzoic acid and pyridine-N-oxide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 6. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65056-1_70.

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Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of oxovanadium(IV) derivative with bis(hydrazone) derived from 1,1′-diacetylferrocene and 4-nitrobenzoic acid hydrazide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 1. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62478-4_39.

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Wootton, John F., and David R. Trentham. "‘CAGED’ Compounds to Probe the Dynamics of Cellular Processes: Synthesis and Properties of some Novel Photosensitive P-2-Nitrobenzyl Esters of Nucleotides." In Photochemical Probes in Biochemistry. Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-0925-0_21.

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Larsen, R. D. "From (2-Nitrobenzoyl)alkanes or (2-Nitrobenzoyl)alkenes." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-01026.

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Conference papers on the topic "Nitrobenzoyl"

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Quraishi, M. A., and V. Bhardwaj. "Inhibition of Metallic Corrosion by Some 2-Cinnamyl Imidazoline Salts under Vapor Phase Conditions." In CORROSION 2003. NACE International, 2003. https://doi.org/10.5006/c2003-03365.

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Abstract Four organic volatile corrosion inhibitors (VCIs) were synthesized using 2-cinnamyl imidazoline with various acids such as salicylic acid, maleic acid, nitrobenzoic acid and phthalic acid and evaluated as corrosion inhibitors of mild steel, brass and copper by weight loss method. Eschke test method, sodium chloride inoculation test method and sulfur dioxide (SO2) test method were also carried out to investigate the corrosion inhibiting effect of the compounds. All the investigated VCIs exhibited good inhibition efficiency (IE) for all the metals. Phthalate salt showed best result amon
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Quraishi, M. A. "Lauric Hydrazide Derivatives: New Class of Volatile Corrosion Inhibitors." In CORROSION 2002. NACE International, 2002. https://doi.org/10.5006/c2002-02319.

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Abstract The protection of metals against corrosion by means of volatile compounds is the most progressive method of fighting metallic corrosion. These inhibitors are used to protect metallic articles and equipment during storage and transportation. In view of this we have synthesized six organic volatile corrosion inhibitors (VCIs) using Lauric hydrazide with various acids such as cinnamic acid, succinic acid, nitrobenzoic acid, phthalic acid and maleic acid and evaluated their inhibiting action on corrosion of mild steel, copper, brass, zinc and aluminium by weight loss and potentiodynamic p
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Santos, Giovanna C., Jéssica B. Macedo, Marcela S. Lopes, Rodrigo M. de Pádua, and Renata B. Oliveira. "Unexpected dimerization of a nitrobenzyl chloride under basic conditions." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_201381974519.

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Houlihan, F. M., A. Shugard, R. Gooden, and E. Reichmanis. "An Evaluation Of Nitrobenzyl Ester Chemistry For Chemical Amplification Resists." In 1988 Microlithography Conferences, edited by Scott A. MacDonald. SPIE, 1988. http://dx.doi.org/10.1117/12.968303.

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Robinson, Hans D., Brenden A. Magill, Xi Guo, et al. "Two-photon activation ofo-nitrobenzyl ligands bound to gold surfaces." In SPIE NanoScience + Engineering, edited by Allan D. Boardman. SPIE, 2014. http://dx.doi.org/10.1117/12.2062226.

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Aldabergenov, M., M. Dauletbekova, G. Toleutay, S. Kudaibergenov, and A. Klivenko. "Reduction of 4-nitrobenzoic acid by AuNPs/Cryogel and PdNPs/cryogel nanocomposites." In 2017 IEEE 7th International Conference "Nanomaterials: Application & Properties" (NAP). IEEE, 2017. http://dx.doi.org/10.1109/nap.2017.8190273.

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Shibana, C., P. Subavathy, K. SenthilKannan, et al. "Growth, computation-structure-elucidation, anti-diabetic use of 1,4-Bis(2-Nitrobenzyl)piperazine(BNBPP) macro, nano crystals." In THE 8TH ANNUAL INTERNATIONAL SEMINAR ON TRENDS IN SCIENCE AND SCIENCE EDUCATION (AISTSSE) 2021. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0108281.

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Houlihan, Francis M., Evelyn Chin, Omkaram Nalamasu, Janet M. Kometani, Thomas X. Neenan та A. Pangborne. "Synthesis, characterization, and lithography of α-substituted 2-nitrobenzyl arylsulfonate photo-acid generators with improved resistance to post-exposure bake". У SPIE's 1994 Symposium on Microlithography, редактор Omkaram Nalamasu. SPIE, 1994. http://dx.doi.org/10.1117/12.175331.

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Saršūns, Kristaps, and Agris Bērziņš. "Computational prediction and experimental confirmation of Solid Solution formation from different nitrobenzoic acid derivatives and their isomers." In The 2nd International Online Conference on Crystals. MDPI, 2020. http://dx.doi.org/10.3390/iocc_2020-07317.

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Al-Jabiri, Mohamad, and Wolfgang Insausti, Jäger. "ROTATIONAL SPECTROSCOPIC STUDIES OF PARA-NITROBENZOIC ACID, PARA-AMINOBENZOIC ACID, PARA-CHLOROBENZOIC ACID, AND PARA-HYDROXYBENZOIC ACID." In 2023 International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2023. http://dx.doi.org/10.15278/isms.2023.6899.

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