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Relevant bibliographies by topics / Sulphonyl derivative

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Academic literature on the topic 'Sulphonyl derivative'

Author: Grafiati

Published: 5 June 2025

Last updated: 15 July 2025

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Journal articles on the topic "Sulphonyl derivative"

1

M.A., METWALLY, Y. YOUSIF M., ISMAIEL A.M., and A. AMER F. "Syntheses of Some Arylsulphonyl Pyrazolines and Pyrazolones as Potential Antipyretic Analgesic Agents." Journal of Indian Chemical Society Vol. 62, Jan 1985 (1985): 54–56. https://doi.org/10.5281/zenodo.6302358.

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University of Mansoura, Mansoura, Egypt <em>Manuscript received 21 February 1984, accepted 15 August 1984</em> Treatment of 3-methyl or 3-phenyl-2-pyrazolin-5-ones (1a, b) with <em>p</em>-acetamido or <em>p</em>-methylbenzenesulphonyl chloride afforded the O-sulphonyl derivatives (3a-d). The N-sulphonyl derivative (6) and N-methyl derivative (8) were also prepared. The 3- anilino derivatives (10a-d) and 3,5-dimethylpyrazoline derivative (13) were prepared. The ir spectral data of the synthesised compounds are discussed.

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2

Mistry, Rakesh N., and K. R. Desai. "Studies on Synthesis of Some Novel Heterocyclic Chalcone, Pyrazoline, Pyrimidine - 2 - One, Pyrimidine - 2 - Thione,para-Acetanilide Sulphonyl and Benzoyl Derivatives and their Antimicrobial Activity." E-Journal of Chemistry 2, no. 1 (2005): 30–41. http://dx.doi.org/10.1155/2005/953107.

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1, 2 - Dichloro benzene on chlorosulphonation by chlorosulphonic acid gives 1, 2 - [dichloro] - benzene sulphonyl chloride which on condensation withp–amino acetophenone gives 1-[acetyl] - 1’ , 2’ - [dichloro] - dibenz sulphonamide derivative. This derivative undergo condensation with 2,4- dichloro benzaldehyde gives 1- [3” - (sub. phenyl) - 2” - propene - 1” - one] - 1’ , 2’ - [dichloro] - dibenz sulphonamide derivative which on reaction with 99% hydrazine hydrate and glacial acetic acid gives 1-[acetyl]-3- [1’ , 2’ - (dichloro) - dibenz sulphonamide] -5 - [2” , 4” - dichloro phenyl] - 2 - py

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3

Goyal, Rakesh, Mukesh Sharma, Dharmendra Ahuja, and Anurekha Jain. "Synthesis and Evaluation of Aldehyde Derivatives of Sulfonyl Chloride Quinoxaline." Journal of Drug Delivery and Therapeutics 9, no. 4-A (2019): 921–27. http://dx.doi.org/10.22270/jddt.v9i4-a.3142.

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In pyrazine mesomeric interaction between the protonated & neutral nitrogen atoms probably destabilizes the cation.N, N’-diprotonation is very easier for pyrazine Synthesis of 2, 3-diphenylquinoxaline by phenylene-diamine in 16 ml of rectified spirit was added & combine solution was warm in water bath for 30 min. added water until slight colorless persist & allow to cool recrystallize the product in ethanol. Synthesis of 2, 3-diphenylquinoxaline 7-sulfonylchloride (R) using chlorosulfonic acid under ice-cold condition, then Synthesis of 2-hydroxyphenyl-2,3-diphenylquinoxaline-7-sul

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4

Ameen, Ban, ASMAA Jawad, and Evon Akram. "Synthesis, In Vitro Biological Activity and Anti-Breast Cancer of Diazepine Derivatives." Al-Kufa University Journal for Biology 16, no. 3 (2024): 88–94. https://doi.org/10.36320/ajb/v16.i3.17437.

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Since their discovery, diazepines have been essential derivatives that can be found in nature or synthesized in laboratories. We synthesized a new diazepine (4-6), namely 2-[4-(4-chlorophenyl)-2,5-dihydro-1H-1,5-benzodiazepin-2-yl]phenol (4), 2-(4-{2-[(dioxo-l6-sulfanyl)oxy]phenyl}-2,5-dihydro-1H-1,5-benzodiazepin-2-yl)phenol (5), and 2-[4-(2-hydroxyphenyl)-4,5-dihydro-1H-1,5-benzodiazepin-2-yl]benzene-1,3-diol (6). These derivatives are synthesized from 2-hydroxy acetophenone with aldehyde derivatives, such as 4-chlorobenzaldehyde, 2-sulfobenzaldehyde, and 2,6-dihydroxybenzaldehyde. The chalc

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5

Sirisha, K*. "Estimation of a New Gabapentin Derivative in Capsule Dosage Form by New Validated UV Spectrophotometric Method." International Journal of Pharmacy and Biological Sciences (IJPBS) 13, no. 3 (2023): 26–35. https://doi.org/10.5281/zenodo.10260625.

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AbstractA new simple, sensitive, and economic spectrophotometric method has been developed and validated for the determination of a new gabapentin derivative in pure form and pharmaceutical preparations. The method is based on the reaction between the amino group of gabapentin with benzene sulphonyl chloride to form the gabapentin derivative (sulphonamide) via addition-elimination mechanism. The new gabapentin derivative was prepared by two different methods using sodium carbonate (method 1) and sodium hydroxide (method 2). The colourless product obtained was analysed by TLC. In UV-spectrophot

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6

Yuksel, Fatma, Sinem Tuncel, and Vefa Ahsen. "Synthesis and characterizations of peripheral octa-amino and octa-amidophthalocyanines." Journal of Porphyrins and Phthalocyanines 12, no. 02 (2008): 123–30. http://dx.doi.org/10.1142/s1088424608000169.

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Novel 2,3,9,10,16,17,23,24-octaamino substituted Ni(II) phthalocyanine (2) was synthesized from tosylamido (tosyl: toluene-p-sulphonyl) derivative by the cleavage of tosyl groups in the presence of 90% sulfuric acid. Octa-hexanoylamido Ni(II) phthalocyanine (3a) and octa-lauroylamido Ni(II) phthalocyanine (3b) were obtained by reacting of octa-amino Ni(II) phthalocyanine (2) with hexanoyl chloride and lauroyl chloride, respectively. The new compounds have been characterized by elemental analysis, FT-IR, NMR and UV-vis spectroscopy and mass spectrometry. The aggregation behaviors of new compoun

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7

Green, J., O. M. Ogunjobi, R. Ramage, A. S. J. Stewart, S. McCurdy, and R. Noble. "Application of the NG-(2,2,5,7,8-pentamethylchroman-6-sulphonyl) derivative of FMOC-arginine to peptide synthesis." Tetrahedron Letters 29, no. 34 (1988): 4341–44. http://dx.doi.org/10.1016/s0040-4039(00)80492-x.

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8

Ramage, R., and J. Green. "NG-2,2,5,7,8-pentamethylchroman-6-sulphonyl-L-arginine: A new acid labile derivative for peptide synthesis." Tetrahedron Letters 28, no. 20 (1987): 2287–90. http://dx.doi.org/10.1016/s0040-4039(00)96103-3.

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9

Ramage, Robert, Jeremy Green, and Alexander J. Blake. "An acid labile arginine derivative for peptide synthesis: NG-2,2,5,7,8-pentamethylchroman-6-sulphonyl-L-arginine." Tetrahedron 47, no. 32 (1991): 6353–70. http://dx.doi.org/10.1016/s0040-4020(01)86564-9.

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10

Melford, C. Egbujor, C. Okoro Uchechukwu, and N. Okafor Sunday. "Novel Alanine-based Antimicrobial and Antioxidant Agents: Synthesis and Molecular Docking." Indian Journal of Science and Technology 13, no. 9 (2020): 1003–14. https://doi.org/10.17485/ijst/2020/v013i09/146687.

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Abstract <strong>Objective:</strong> To synthesize new alanine-based phenyl sulphonamide derivatives with significant antimicrobial and antioxidant activities. <strong>Methods:</strong> The reaction of alanine with benzene sulphonyl chloride afforded compound <strong>3a</strong>. The ammonolysis of its N-acylated derivative gave the carboxamide which yielded the aryl/heteroaryl derivatives compounds <strong>3d</strong>, <strong>3e</strong>, and <strong>3f</strong> via Buchwald–Hartwig nickel catalyzed amidation reaction. Structures agreed with the spect

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Dissertations / Theses on the topic "Sulphonyl derivative"

1

Farouk, Sultan. "A study of 1,3-dipolar cycloadditions as a route to novel pesticides." Thesis, University of Hertfordshire, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.338561.

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Al-Jebouri, Hamza Yaseen. "Synthesis of butadiene sulphone derivatives with cyano substituents." Thesis, University of Surrey, 1985. http://epubs.surrey.ac.uk/847181/.

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The vicinal dicyano compounds are good starting materials for the synthesis of macromolecules such as phthalocyanines and tetrazaporphins. The synthesis of cyano compounds and vicinal dicyano compounds, particularly the cyano derivatives of butadiene sulphones have been studied in this work. This thesis is divided into five chapters as follows: The first chapter contains a general introduction about organic cyanides; their preparations, reactions and applications. In the second chapter, the synthesis of butadiene sulphone derivatives leading to mono and dicyano substituents is dealt with. It i

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3

Bassin, Jatinder Paul. "Chlorosulphonic acid in heterocyclic synthesis-cyclic sulphones and ketoarylidene derivatives." Thesis, University of Hertfordshire, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.303497.

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4

Molapo, Kerileng Mildred. "Electrochemiluminescence and organic electronics of derivatised poly(aniline sulphonic acid) light-emitting diodes." University of the Western Cape, 2011. http://hdl.handle.net/11394/5422.

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>Magister Scientiae - MSc<br>Applications of electrochemiluminescent conjugated polymers offer promising solutions in addressing the problem of light emitting devices. However, the challenging problems that hamper their application in light emitting devices are loss of signal due to diffusion of the electrochemiluminescence (ECL) reagent out of the detection zone, limited ability to repeatedly cycle an individual luminophore and high reagent consumption. In this work, the main objective was to produce conducting polymers with enhanced electrochemiluminescence by tuning the properties of the po

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Molapo, Kerileng Mildred. "Electro chemiluminescence and organic electronics of derivatised poly(aniline sulphonic acid) light-emitting diodes." University of the Western Cape, 2011. http://hdl.handle.net/11394/8437.

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>Magister Scientiae - MSc<br>Electrochemiluminescence (EeL) is applied for industrial applications that have considerable potential, such as clinical diagnostic, analytical chemistry, and light-emitting devices, due to selectivity, sensitivity for detection and quantification of molecules through generation of fluorescence light when electric current is applied on the materials. In EeL the electrochemical reaction allows for precise control over the time and position of the light emitting reaction. The control over time allows one to synchronise the luminescence and the biochemical reaction u

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6

Lin, Yi-Feng, and 林義峰. "Part Ⅰ Synthesis and Photochemistry of a series of radical pair precursors contain 1-toluene sulphonyl benzimidazoles and their derivatives Part Ⅱ Synthesis of (4,4´-dicarboxylate-2,2´-bipyridyl) ruthenium complexes applied in the solar cell." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/45209660368849627531.

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碩士<br>國立交通大學<br>應用化學系所<br>93<br>The major part of this thesis is about the syntheses and EPR studies of a series of radical pair precursors (55, 56 and 57) which contain 1-toluene sulphonyl benzimidazoles as the key components. The photolysis (230-325 nm) of 55 at 77 K in a MTHF matrix gave EPR signals characteristic of a randomly oriented triplet radical pair and its zero-field splitting parameters are determined to be |D/hc| = 0.0144 cm-1 and |E/hc| = 0.0020 cm-1, respectively. Furthermore, the photolysis of 55 in the presence of MNP in CDCl3 at room temperature gave not only the Photo-Fries

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Books on the topic "Sulphonyl derivative"

1

Patai, Saul, and Zvi Rappoport, eds. Sulphonic Acids, Esters and their Derivatives (1991). John Wiley & Sons, Ltd, 1991. http://dx.doi.org/10.1002/0470034394.

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2

Saul, Patai, and Rappoport Zvi, eds. The Chemistry of sulphonic acids, esters, and their derivatives. Wiley, 1991.

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3

Chemistry of Sulphonic Acids, Esters and Their Derivatives. Wiley & Sons, Incorporated, John, 2021.

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4

Patai, Saul, and Zvi Z. Rappoport. Chemistry of Sulphonic Acids, Esters and Their Derivatives. Wiley & Sons, Limited, John, 2006.

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5

Chemistry of Sulphonic Acids Esters and their Derivatives. Wiley & Sons, Limited, John, 2009.

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6

The chemistry of sulphonic acids, esters and their derivatives. Wiley, 1991.

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Book chapters on the topic "Sulphonyl derivative"

1

Mariani, M., A. Paio, M. Ciomei, et al. "In vitro activity of novel sulphonic derivatives of distamicyn A." In Experientia Supplementum. Birkhäuser Basel, 1992. http://dx.doi.org/10.1007/978-3-0348-7001-6_76.

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2

Sola, F., G. Biasoli, E. Pesenti, et al. "In vivo activity of novel sulphonic derivatives of distamycin A." In Experientia Supplementum. Birkhäuser Basel, 1992. http://dx.doi.org/10.1007/978-3-0348-7001-6_77.

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3

"Sulphonic Acids and Their Derivatives." In Lectures on Organic Chemistry. IMPERIAL COLLEGE PRESS, 1997. http://dx.doi.org/10.1142/9781848160903_0026.

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4

"Carboxylic Acid or its Derivative and a Sulphinic or Sulphonic Acid Derivative." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187302.ch75.

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