Relevant bibliographies by topics / Nitrobenzyle chloride

Contents

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

Academic literature on the topic 'Nitrobenzyle chloride'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 May 2024

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Nitrobenzyle chloride.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Nitrobenzyle chloride"

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.

Full text
Abstract:
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
APA, Harvard, Vancouver, ISO, and other styles
2

Look, Kai, and Robert K. Norris. "Formation by SRN1 Reactions and 1H N.M.R. Properties of Sterically Encumbered 2,4,6-Trialkylphenyl p-Nitrobenzyl Sulfides." Australian Journal of Chemistry 52, no. 11 (1999): 1077. http://dx.doi.org/10.1071/ch99080.

Full text
Abstract:
Sterically hindered p-nitrobenzylic chlorides (1) and (2) react with the sodium salts of 2,4,6-trialkylbenzenethiols (3a)–(5a) by the SRN1 reaction to give good yields of the corresponding p-nitrobenzylic aryl sulfides (6)–(10). For example, the reaction of sodium 2,4,6-triisopropylbenzenethiolate (4b) with α-t-butyl-a-methyl-p-nitrobenzyl chloride (2) gives the sulfide (10) in over 80% yield after 2 h at room temperature in Me2SO. Only in reactions involving 2,4,6-tri-t-butylbenzenethiol (5a) are low yields or failed reactions encountered. Qualitative examination of the dynamic nuclear magnet
APA, Harvard, Vancouver, ISO, and other styles
3

Matyushkina, Yulia I., and Alexandr A. Shabarin. "EXTRACTION OF ANIONIC CADMIUM COMPLEXES WITH ORGANIC SOLUTIONS OF QUATERNARY AMMONIUM SALTS." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENII KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 63, no. 10 (2020): 30–35. http://dx.doi.org/10.6060/ivkkt.20206310.6224.

Full text
Abstract:
The anion-exchange extraction of thiocyanate, chloride and iodide cadmium complexes by solutions of quaternary ammonium salts chlorides in organic solvents (toluene, carbon tetrachloride, ethyl acetate, isobutyl alcohol, nitrobenzene) was studied. Extraction involves solutions of alkyl dimethylbenzylammonium chlorides (R-N+(CH3)2-CH2C6H5-Cl-) and alkyl dimethylethyl-benzylammonium (R-N+(CH3)2-CH2-CH2C6H5-Cl-), where R is a straight alkyl chain, mainly C12 - C14. The composition of the cadmium anionic complexes was established by the analysis of the calibration curves E = f (pCCd (II)) construc
APA, Harvard, Vancouver, ISO, and other styles
4

Utami, Dwi, Iin Narwanti, and Jumina Jumina. "SINTESIS SENYAWA ANTIMALARIA BARU TURUNAN FENANTROLIN N-(2-NITROBENZIL)-1,10-FENANTROLINIUM IODIDA DAN (1) N-(4-NITROBENZIL)-1,10-FENANTROLINIUM IODIDA." Molekul 9, no. 1 (2014): 84. http://dx.doi.org/10.20884/1.jm.2014.9.1.153.

Full text
Abstract:
Malaria is a global health problem, especially in the tropics. Efforts to decrease the incidence of malaria plagued the plasmodium resistance to existing antimalarial drugs. Benzyl Phenanthrolium Iodide derivates have been proved has antimalarial activity. The aim of this study is synthesis the nitro benzyl phenanthrolium.The research that has been done was the synthesis of (1)-N-(2-nitrobenzyl) phenantrolium iodide and(1)-N-(4-nitrobenzyl)-1,10-phenantrolium iodide. Synthesis of (1)-N-(2-nitrobenzyl)-1,10-phenantrolium iodide through a two-steps reaction SN-2 is the reaction of (1)N-(2- nitro
APA, Harvard, Vancouver, ISO, and other styles
5

Matyushkina, Yulia I., and Alexandr A. Shabarin. "STUDY OF ANION EXCHANGE EXTRACTION OF SOME ANIONIC COMPLEXES OF IRON (III) BY ORGANIC SOLUTIONS OF QUARTERLY AMMONIUM SALTS." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENII KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 62, no. 2 (2019): 25–30. http://dx.doi.org/10.6060/ivkkt.20196202.5782.

Full text
Abstract:
The anion-exchange extraction of salicylate, thiosulphate and thiocyanate iron (III) complexes by solutions of chlorides of quaternary ammonium salts (QAS) in organic solvents (toluene, carbon tetrachloride, ethyl acetate, isobutyl alcohol, nitrobenzene) was studied. The composition of the iron (III) anionic complexes was established by the analysis of the calibration curves E = f(pCFe (III)) constructed from iron (III) solutions against the background of various contents of thiocyanate, thiosulphate and salicylate ions and the steepness of the electrode function. As an indicator electrode the
APA, Harvard, Vancouver, ISO, and other styles
6

Raza, Ali, Zaka Ullah, Adnan Khalil, et al. "Facile fabrication of a graphene-based chemical sensor with ultrasensitivity for nitrobenzene." RSC Advances 14, no. 14 (2024): 9799–804. http://dx.doi.org/10.1039/d3ra08794h.

Full text
Abstract:
A graphene-based chemical sensor is fabricated which offers a notable response for nitrobenzene. The sensor shows the highest sensitivity of 231.1 for nitrobenzene and the fastest response of 6.9 s for benzyl chloride.
APA, Harvard, Vancouver, ISO, and other styles
7

Moreno, S. N., J. Schreiber, and R. P. Mason. "Nitrobenzyl radical metabolites from microsomal reduction of nitrobenzyl chlorides." Journal of Biological Chemistry 261, no. 17 (1986): 7811–15. http://dx.doi.org/10.1016/s0021-9258(19)57473-7.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Boyle, Grant A., Hendrik G. Kruger, Glenn E. M. Maguire, and Jason Paraskevopoulos. "(4-Hydroxy-3-nitrobenzyl)methylammonium chloride." Acta Crystallographica Section E Structure Reports Online 64, no. 3 (2008): o625. http://dx.doi.org/10.1107/s160053680800473x.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Patel, N. Z., J. N. Patel, and R. M. Patel. "Synthesis and Biological Activity of Polyketone Resins-IV. Systems Based on m-Xylene with Nitrobenzene as Solvent." High Performance Polymers 4, no. 3 (1992): 141–49. http://dx.doi.org/10.1088/0954-0083/4/3/002.

Full text
Abstract:
Seven chlorine-terminated polyketones of low molecular weight were prepared from m-xylene, chloroacetyl chloride and ao-dichloroalkanes, i.e. dichloro-methane and 1,2-dichloroethane, by the Friedel-Crafts reaction using nitrobenzene as solvent. The polyketones were characterized by [R spectra and vapour pressure osmome-t'y. The thermal properties were studied by thermogravimetry and differential scanning calorimetry. The kinetic parameters for the decomposition reactions were evaluated by the Broido and Doyle methods. The polyketones were found to be thermally sable up to 220°C but decompose b
APA, Harvard, Vancouver, ISO, and other styles
10

Hoffmann, M. "Synthesis of Phosphonodidepsipeptides through Esterification of [1-(Benzyloxycarbonylamino)alkyl]phosphonic Acids." Australian Journal of Chemistry 41, no. 4 (1988): 605. http://dx.doi.org/10.1071/ch9880605.

Full text
Abstract:
The synthesis is reported of phosphonodidepsipeptides (3) through esterification of [1-( benzyloxycarbonylamino )alkyl] phosphonic acids (1) with α- hydroxy acid p-nitrobenzyl esters (2) in the presence of thionyl chloride in dimethylformamide.
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Nitrobenzyle chloride"

1

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

Full text
Abstract:
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 -halogénoesters et -halogénoamides en série nitrobenzylique. Cette méthodol
APA, Harvard, Vancouver, ISO, and other styles
2

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

Full text
Abstract:
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 -halogénoesters et -halogénoamides en série nitrobenzylique. Cette méthodol
APA, Harvard, Vancouver, ISO, and other styles
3

Roche, Manon. "Pharmacochimie radicalaire à visée antirhinovirale." Thesis, Aix-Marseille, 2013. http://www.theses.fr/2013AIXM5507.

Full text
Abstract:
Ce travail de pharmacochimie est consacré à la synthèse de nouvelles molécules benzéniques en vue d’étudier leurs propriétés pharmacologiques in vitro sur le Rhinovirus humain 14 mais également d’en déduire des relations de structure activité. En effet, le fil conducteur du projet de thèse est un travail de pharmacomodulation en collaboration avec le Rega Institute for Medical Research de Louvain. La méthode principale de synthèse de ces structures est basée sur la méthodologie TDAE ou Tétrakis(DiméthylAmino)Ethylène, appliquée sur des substrats dérivés du chlorure de nitrobenzyle. La synthèse
APA, Harvard, Vancouver, ISO, and other styles
4

Roche, Manon. "Pharmacochimie radicalaire à visée antirhinovirale." Electronic Thesis or Diss., Aix-Marseille, 2013. http://www.theses.fr/2013AIXM5507.

Full text
Abstract:
Ce travail de pharmacochimie est consacré à la synthèse de nouvelles molécules benzéniques en vue d’étudier leurs propriétés pharmacologiques in vitro sur le Rhinovirus humain 14 mais également d’en déduire des relations de structure activité. En effet, le fil conducteur du projet de thèse est un travail de pharmacomodulation en collaboration avec le Rega Institute for Medical Research de Louvain. La méthode principale de synthèse de ces structures est basée sur la méthodologie TDAE ou Tétrakis(DiméthylAmino)Ethylène, appliquée sur des substrats dérivés du chlorure de nitrobenzyle. La synthèse
APA, Harvard, Vancouver, ISO, and other styles
5

Gérard, Hervé. "Mise en évidence d'une réaction de déshalogénation catalysée par l'hémoglobine." Compiègne, 1989. http://www.theses.fr/1989COMPD194.

Full text
Abstract:
L'hémoglobine, hémoprotéine à protoporphyrines IX peut dans des conditions définies catalyser des réactions typiques du cytochrome P 450. L'hémoglobine en présence d'acide ascorbique déshalogéner de nombreux organochlorés. Le chlorure de paranitrobenzyle est déshalogéné en paranitrotoluène par l'hémoglobine humaine. Le DDT et le perchloroéthane sont aussi substrat de cette réaction. L'étude mécanistique de cette réaction montre le caractère réductif oxygène dépendante de cette déshalogénation. Un schéma réactionnel est proposé afin d'expliquer les inhibitions de la réaction par la superoxyde d
APA, Harvard, Vancouver, ISO, and other styles

Book chapters on the topic "Nitrobenzyle chloride"

1

Winkelmann, J. "Diffusion of hydrogen chloride (1); nitrobenzene (2)." In Gases in Gases, Liquids and their Mixtures. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_1525.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Smellie, Iain A., Matt L. Clarke, Leanne Harris, and Andrew J. Miller. "3.1.3. Synthesis and Characterisation of an Ester from 4-Nitrobenzoyl Chloride." In Comprehensive Organic Chemistry Experiments for the Laboratory Classroom. The Royal Society of Chemistry, 2016. http://dx.doi.org/10.1039/9781849739634-00136.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Taber, Douglass F. "Substituted Benzenes: The Alvarez- Manzaneda Synthesis of (–)-Akaol A." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0063.

Full text
Abstract:
Ramin Ghorbani-Vaghei of Bu-Ali Sina University devised (Tetrahedron Lett. 2012, 53, 2325) conditions for the bromination of an electron-deficient arene such as 1. Yonghong Gu of the University of Science and Technology of China found (Tetrahedron Lett. 2011, 52, 4324) that an electron-rich anilide 3 could be oxidized to 4. Sukbok Chang of KAIST (J. Am. Chem. Soc. 2012, 134, 2528) and Kouichi Ohe of Kyoto University (Chem. Commun. 2012, 48, 3127) devised protocols for the oxidative cyanation of 5 to 6. Phenylazocarboxylates and triazenes are stable, but have the reaction chemistry of diazonium salts. The aromatic substitution chemistry of these derivatives has not been much explored. As illustrated by the conversion of 7 to 8, reported (J. Org. Chem. 2012, 77, 1520) by Markus R. Heinrich of the Universität Erlangen-Nürnberg, the benzene ring of the phenylazocarboxylate is reactive with nucleophiles. In contrast, triazene-activated benzene rings should be particularly reactive with electrophiles, as exemplified by the transformation, below, of 20 to 21. Melanie S. Sanford of the University of Michigan observed (Org. Lett. 2012, 14, 1760) good selectivity for 12 in the Pd-catalyzed reaction of 10 with 11. Jérôme Waser of the Ecole Polytechnique Fédérale de Lausanne used (Org. Lett. 2012, 14, 744) 14 to alkynylate 13 to give 15. Sulfonyl chlorides such as 16 are readily prepared from the corresponding arene, and many are commercially available. Jiang Cheng of Wenzhou University found (Chem. Commun. 2012, 48, 449) conditions for the direct cyanation of 16 to 17. Kenneth M. Nicholas of the University of Oklahoma effected (J. Org. Chem. 2012, 77, 5600) selective ortho bromination of the carbamate 18 to give 19. Stefan Bräse of KIT observed (Angew. Chem. Int. Ed. 2012, 51, 3713) ortho trifluoromethylation of the triazene 20 to give 21. Ji-Quan Yu of Scripps/La Jolla designed (Nature 2012, 486, 518) the benzyl ether 22 to activate the arene for C–C bond formation at the meta position to give 23. Guo-Jun Deng of Xiangtan University employed (Org. Lett. 2012, 14, 1692) a borrowed hydrogen strategy to effect aromatization of 24 with nitrobenzene to give the aniline 25.
APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Nitrobenzyle chloride"

1

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Nitrobenzyle chloride' for particular source types:
Journal articles
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography