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Relevant bibliographies by topics / Chloroacetoxy derivatives

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Journal articles

Academic literature on the topic 'Chloroacetoxy derivatives'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Chloroacetoxy derivatives"

1

Musayeva, B. I., V. M. Farzaliyev, G. G. Ismayilova, N. N. Novotorzhina, and M. R. Safarova. "Mixed esters of xanthogenic acids containing carbonyl, dithiocarbamine and thiocyane group and their research as additives improving tribological characteristics." World of Oil products the Oil Companies Bulletin 04, no. 1 (2021): 60–64. http://dx.doi.org/10.32758/2071-5951-2021-1-4-60-64.

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On the basis of environmentally friendly raw materials of glycerol, by its interaction with monochloroacetic acid, 1,2,3-(trichloroacetyl)triglyceride was synthesized, which is used for further syntheses of xanthogenic acid derivatives containing a number of functional groups  dithiocarbamic, thiocyanic. The reaction of 1,2,3-(trichloroacetyl) triglyceride with potassium alkylxanthate in a ratio of 1:1 and 1:2 gave 1-butylxanthogenatoacetoxy-2,3-(dichloroacetoxy) propane and 1,3-di(alkylxanthogenatoacetoxy)-2-chloroacetoxypropane. Mixed esters of xanthogenic acid containing dithiocarbamic and

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2

Yassin, Fathy A. "Synthesis of New Thieno- and Pyrazolo- pyridazine Derivatives." Journal of Chemical Research 2005, no. 4 (2005): 270–73. http://dx.doi.org/10.3184/0308234054213474.

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5,6-Di(pyridin-2-yl)-3-thioxo-2,3-dihydropyridazine-4-carbonitrile 2 has been reacted with ahalocompounds, such as chloroacetone, chloroacetamide, ethyl chloroacetate and chloroacetic acid gave the corresponding 2-S-alkylated pyridazine derivatives 3, 6, 10 and 13 which have been cyclised to give the corresponding thienopyridazine derivatives 4, 7, 11, and 14 respectively. Reaction of 15 with hydrazine hydrate gave the corresponding pyrazolopyridazine 16.

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3

Tolba, Mahmoud S., Mostafa Sayed, Shaban A. A. Abdel-Raheem, Taher A. Gaber, Adel M. Kamal El-Dean, and Mostafa Ahmed. "Synthesis and spectral characterization of some new thiazolopyrimidine derivatives." Current Chemistry Letters 10, no. 4 (2021): 471–78. http://dx.doi.org/10.5267/j.ccl.2021.4.004.

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Thiazolopyrimidnes are considered one of the most interesting classes in heterocyclic chemistry due to their pharmaceutical importance. Herein, we report the synthesis of some new heterocyclic compounds containing thiazolopyrimidine starting from compound (1) which was previously prepared in literature. The starting compound was allowed to react with different alkylating agents such as chloroacetone, chloroacetyl chloride, and phenacyl bromide to afford derivatives (2-4). Compound (5), benzylidene derivative, was obtained by the reaction of compound (2) with benzaldehyde while amino-dicarbonit

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4

Athraa H Mekky and Sajida M Thamir. "Synthesis, characterisation and antibacterial evaluation of some novel 1-phenyl-1h-tetrazole-5-thiol derivatives." International Journal of Research in Pharmaceutical Sciences 10, no. 2 (2019): 1136–42. http://dx.doi.org/10.26452/ijrps.v10i2.394.

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The aim of the study is to synthesise and. Characterize — some novel, "tetrazole., -5-thiol” derivatives. Firstly, the “1-phenyl-1H7-tetrazole-5-thiol” (A1) has been., synthesised by the reaction of phenylisothiocyanate with NaN3 in water as a solvent. Secondly, the tetrazole-5-thiol derivatives (A2-A4) were synthesised by the alkylation reaction of the compound (A1) with chloroacetone, phenacyl bromide and chloromethyl acetate respectively. The resulted percentage yield was relatively high (92%, %95, %90 respectively). Compound (A5) was synthesised by the reaction of ethyl acetate tetrazole d

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5

Darwish, Elham S. "Facile Synthesis and Antimicrobial Evaluation of Some New Heterocyclic Compounds Incorporating a Biologically Active Sulfamoyl Moiety." Scientific World Journal 2014 (2014): 1–10. http://dx.doi.org/10.1155/2014/165495.

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A facile and convenient synthesis of new heterocyclic compounds containing a sulfamoyl moiety suitable for use as antimicrobial agents was reported. The precursor 3-oxo-3-phenyl-N-(4-sulfamoylphenyl)propionamide was coupled smoothly with arenediazonium salt producing hydrazones which reacted with malononitrile or triethylorthoformate affording pyridazine and triazine derivatives, respectively. Also, the reactivity of the same precursor with DMF-DMA was followed by aminotriazole; aromatic aldehydes was followed by hydrazine hydrate, triethylorthoformate, or thiourea affording triazolo[1,5-a]pyr

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6

Salem, Mohamed A., Samir Y. Abbas, Marwa A. M. Sh El-Sharief, et al. "Novel Structural Hybrids of Pyrrole and Thiazole Moieties: Synthesis and Evaluation of Antibacterial and Antifungal Activities." Acta Chimica Slovenica 68, no. 4 (2021): 990–96. http://dx.doi.org/10.17344/acsi.2021.6980.

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One of the best ways to design new biocidal agents is synthesizing hybrid molecules by combining two or more bioactive moieties in a single molecular scaffold. So, new series of pyrroles bearing a thiazole moiety were synthesized using 1-methyl-1H-pyrrole-2-carbaldehyde thiosemicarbazones 1a–c. Cyclization of thiosemicarbazone derivatives 1a–c with ethyl chloroacetate, ethyl 2-chloropropanoate, chloroacetone and phenacyl bromide afforded the corresponding thiazolidin-4-ones 2a–c, 5-methylthiazolidin-4-ones 3a–c, 4-methyl-2,3-dihydrothiazoles 4a–c, and 4-phenyl-2,3-dihydrothiazoles 5a–c, respec

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7

Hradil, Pavel, Jan Vaněček, Jan Hlaváč, and Juraj Ševčík. "Synthesis of 2-Substituted-6,7-dimethoxy- and 6,7,8-Trimethoxy-3-hydroxyquinolin-4(1H)-ones." Collection of Czechoslovak Chemical Communications 64, no. 2 (1999): 257–64. http://dx.doi.org/10.1135/cccc19990257.

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Acetonyl and phenacyl esters of 4,5-dimethoxy- and 3,4,5-trimethoxyanthranilic acids 3 were prepared by reduction of corresponding nitro derivatives 2. Acetonyl 4,5-dimethoxyanthranilate (3a) was prepared by reaction of 4,5-dimethoxyanthranilic acid and chloroacetone. Cyclization of these acetonyl and phenacyl esters in polyphosphoric acid provided the corresponding 2-substituted-6,7-dimethoxy- and 6,7,8-trimethoxy-3-hydroxyquinolin-4(1H)-ones 4. A new method of the thermal cyclization is also described. The structure of the prepared compounds was confirmed by 1H NMR spectroscopy.

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8

El-Hagrassey, Eman A., Ehab Abdel-Latif, and Gamal M. Abdel-Fattah. "Synthesis and efficiency of new pyridine, chromene and thiazole containing compounds as antimicrobial and antioxidant agents." Bulletin of the Chemical Society of Ethiopia 36, no. 1 (2022): 137–48. http://dx.doi.org/10.4314/bcse.v36i1.12.

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ABSTRACT. The versatile scaffold, N'-(2-cyanoacetyl)-2-hydroxybenzohydrazide (3) was utilized in the production of new pyridine, chromene and thiazole derivatives as antimicrobial and antioxidant agents. The synthetic strategy involves the treatment of precursor 3 with various arylidene-malononitrile and 3-aryl-2-cyanoacrylate compounds to furnish substituted pyridines 5 and 7. The interaction of 3 with salicylaldehyde and/or phenyl isothiocyanate followed by cyclization with chloroacetone produced the corresponding 2-imino-2H-chromene-3-carbohydrazide and (thiazol-2-ylidene-acetyl)-salicylic

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9

Murat Saracoglu, Murat Saracoglu, Zulbiye Kokbudak Zulbiye Kokbudak, and Zeynep imen and Fatma Kandemirli Zeynep imen and Fatma Kandemirli. "Synthesis and DFT Quantum Chemical Calculations of Novel Pyrazolo[1,5-c]pyrimidin-7(1H)-one Derivatives." Journal of the chemical society of pakistan 41, no. 3 (2019): 479. http://dx.doi.org/10.52568/000746/jcsp/41.03.2019.

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In this study, a convenient procedure for the preparation of pyrazolo[1,5-c]pyrimidin-7(1H)-one derivatives is described. The new pyrazolo[1,5-c]pyrimidin-7(1H)-one derivatives (2a, b) were synthesized from the cyclocondensation reaction of the compounds 1-amino-5-(4-methoxybenzoyl)-4-(4-methoxyphenyl)pyrimidin-2(1H)-one (1a) and 1-amino-5-(4-methylbenzoyl)-4-(4-methylphenyl)pyrimidin-2(1H)-one (1b) with α-chloroacetone. The structures of the compounds (2a, b) were characterized by elemental analysis, FT-IR, 1H-NMR and 13C-NMR spectroscopic techniques. In addition to experimental study in orde

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10

M., B. Deshmukh, S. Jagtap S., A. Deshmukh S., D. Jadhav S., V. Anbhule P., and W. Suryawanshi A. "Synthesis and biological activity of some benzothiazolyl thiazolidinones." Journal of Indian Chemical Society Vol. 84, May 2007 (2007): 498–500. https://doi.org/10.5281/zenodo.5820289.

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Department of Chemistry, Shivaji University, Kolhapur-416 004, Maharashtra, India <em>E-mail</em> : m_deshmukhl@rediffmail.com <em>Manuscript received 1 June 2006, accepted 22 March 2007</em> A facile route for the synthesis of some thiazolidinone derivatives incorporating a benzothiazole moiety has been reported. <em>S</em>-(2-Propanoyl)-1,3-benzothiazole (2) was synthesized by reacting 2-mercapto benzothiazole with chloroacetone in dry acetone, which was subsequently reacted with substituted aryl hydrazides to give the corresponding hydrazones (3}. These on cyclocondensation with mercaptoace

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