Relevant bibliographies by topics / Acetohydrazide

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  3. Conference papers

Academic literature on the topic 'Acetohydrazide'

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

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Journal articles on the topic "Acetohydrazide"

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Hoan, Duong Quoc. "SYNTHESIS AND BIOLOGICAL ACTIVITY EVALUATION OF SOME DERIVATIVES SYNTHESIZED FROM CURCUMIN AND CURCUMIN ANALOG." Hue University Journal of Science: Natural Science 126, no. 1B (2017): 127. http://dx.doi.org/10.26459/hueuni-jns.v126i1b.4139.

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The acetohydrazides <strong>A5 </strong>containing an isoxazole ring and<strong> B5</strong> containing an indazole ring were synthesized from the corresponding acetohydrazide derivatives with acetic anhydride in about 80% high yield. Also, two acetohydrazones <strong>B6</strong> and <strong>B7</strong> were driven from acetohydrazide <strong>B4</strong> by condensation reaction. Bioactivity testes showed that none of them were active against on bacteria except acetohydrazones <strong>B7</strong> showing moderate reactivit
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Aleksandrova, K. V., Ye K. Mykhalchenko, O. S. Shkoda, and D. A. Vasyliev. "Synthesis and physical-chemical properties of (3-benzyl-8-propylxanthin-7-yl)acetohydrazide derivatives and their evaluation for antimicrobial and diuretic activities." Current issues in pharmacy and medicine: science and practice 14, no. 1 (2021): 17–22. http://dx.doi.org/10.14739/2409-2932.2021.1.226742.

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One of the most important tasks of our indigenous pharmaceutical science is the necessity for new medicines because existing drugs are characterized by various side effects, resistance, high toxicity, and so on. New bioactive molecule synthesis utilizes substances of natural origin as well as chemically modified ones. Thus, the researcher’s attention is mainly focused on 3-,7-,8-substituted derivatives of the natural heterocyclic xanthine system, which possess a wide range of pharmacological action. Synthesis of a novel of (3-benzyl-8-propylxanthin-7-yl)acetohydrazides with antimicrobial and d
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Fuloria, Neeraj Kumar, Vijender Singh, M. Shaharyar, and Mohd Ali. "SYNTHESIS AND ANTIMICROBIAL STUDIES OF NOVEL IMINES AND OXADIAZOLES." SOUTHERN BRAZILIAN JOURNAL OF CHEMISTRY 16, no. 16 (2008): 11–22. http://dx.doi.org/10.48141/sbjchem.v17.n17.2008.14_2008.pdf.

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N-benzylidene-2-(4-chloro-3-methylphenoxy)acetohydrazides (3a-e), obtained by arylation of 2-(4-chloro-3-methyl phenoxy)acetohydrazide (2), was cyclized with acetic anhydride to yield 1-(5-(( 4-chloro-3-methylphenoxy)methyl)-2-phenyl-l ,3,4-oxadiazol- 3(2H)-yl)ethanones (4a-e). All the newly synthesized compounds were analytically and spectrally characterized and evaluated for anti-bacterial and anti-fungal activities.
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Zhou, Bao-Han. "Acetohydrazide." Acta Crystallographica Section E Structure Reports Online 65, no. 11 (2009): o2821. http://dx.doi.org/10.1107/s1600536809042469.

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Mor, Satbir, Suchita Sindhu, Mohini Khatri, Ravinder Punia, and Komal Jakhar. "Synthesis, Type II diabetes inhibitory activity, antimicrobial evaluation, and docking studies of N'-arylidene-2-((7-methylbenzo[4,5]thiazolo[2,3-c] [1,2,4]triazol-3-yl)thio)acetohydrazides." European Journal of Chemistry 13, no. 4 (2022): 426–34. http://dx.doi.org/10.5155/eurjchem.13.4.426-434.2315.

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N'-Arylidene-2-((7-methylbenzo[4, 5]thiazolo[2,3-c][1, 2, 4]triazol-3-yl)thio)acetohydrazides (6a-j) were prepared by condensation of 2-((7-methylbenzo[4,5]thiazolo[2,3-c][1,2,4] triazol-3-yl)thio)acetohydrazide with appropriately substituted benzaldehydes in dry methanol and a catalytic amount of glacial acetic acid. The prepared compounds tested for in vitro Type II diabetes inhibition and antimicrobial (antibacterial and antifungal) activities employing α-amylase inhibition assay and the serial dilution method, respectively. Type II diabetes inhibitory assay results of all the tested deriva
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Lokanath, N. K., M. A. Sridhar, J. Shashidhara Prasad, H. S. Nagaraja, and P. Mohan Rao. "(2,4-Dichlorophenoxy)acetohydrazide." Acta Crystallographica Section C Crystal Structure Communications 54, no. 5 (1998): 669–70. http://dx.doi.org/10.1107/s0108270197018416.

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Vu Quoc, Trung, Linh Nguyen Ngoc, Duong Tran Thi Thuy, et al. "Crystal structure of two N′-(1-phenylbenzylidene)-2-(thiophen-3-yl)acetohydrazides." Acta Crystallographica Section E Crystallographic Communications 75, no. 8 (2019): 1090–95. http://dx.doi.org/10.1107/s2056989019008892.

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The synthesis, spectroscopic data, crystal and molecular structures of two N′-(1-phenylbenzylidene)-2-(thiophen-3-yl)acetohydrazides, namely N′-[1-(4-hydroxyphenyl)benzylidene]-2-(thiophen-3-yl)acetohydrazide, C13H10N2O2S, (3a), and N′-[1-(4-methoxyphenyl)benzylidene]-2-(thiophen-3-yl)acetohydrazide, C14H14N2O2S, (3b), are described. Both compounds differ in the substituent at the para position of the phenyl ring: –OH for (3a) and –OCH3 for (3b). In (3a), the thiophene ring is disordered over two orientations with occupancies of 0.762 (3) and 0.238 (3). The configuration about the C=N bond is
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SOGO, Masahiro. "2-(Trimethylammonio)acetohydrazide Chloride." Journal of Synthetic Organic Chemistry, Japan 52, no. 6 (1994): 539–40. http://dx.doi.org/10.5059/yukigoseikyokaishi.52.539.

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Lv, Lu-Ping, Tie-Ming Yu, Wen-Bo Yu, Wei-Wei Li, and Xian-Chao Hu. "N′-(3,4-Dimethoxybenzylidene)acetohydrazide." Acta Crystallographica Section E Structure Reports Online 65, no. 8 (2009): o1989. http://dx.doi.org/10.1107/s1600536809027366.

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Zhou, Bao-Cheng, Lu-Ping Lv, Wen-Bo Yu, Wei-Wei Li, and Xian-Chao Hu. "N′-(3,4-Dimethoxybenzylidene)acetohydrazide." Acta Crystallographica Section E Structure Reports Online 65, no. 8 (2009): o1964. http://dx.doi.org/10.1107/s1600536809028608.

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Book chapters on the topic "Acetohydrazide"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) bromo complex with N′-(furan-3-ylmethylene)-2-(4-methoxyphenylamino)acetohydrazide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_194.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) chloro complex with N′-(furan-3-ylmethylene)-2-(4-methoxyphenylamino)acetohydrazide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_265.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) acetato complex with N′-(furan-3-ylmethylene)-2-(4-methoxyphenylamino)acetohydrazide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_196.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) chloro complex with N′-(furan-3-ylmethylene)-2-(4-methoxyphenylamino)acetohydrazide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_367.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) nitrato complex with N′-(furan-3-ylmethylene)-2-(4-methoxyphenylamino)acetohydrazide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_368.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) acetato complex with N′-(furan-3-ylmethylene)-2-(4-methoxyphenylamino)acetohydrazide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_369.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) nitrato complex with N′-(furan-3-ylmethylene)-2-(4-methoxyphenylamino)acetohydrazide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_195.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) nitrato complex with N′-(furan-3-ylmethylene)-2-(4-methoxyphenylamino)acetohydrazide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_266.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) acetato complex with N′-(furan-3-ylmethylene)-2-(4-methoxyphenylamino)acetohydrazide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_267.

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Lindsley, C. W., and M. E. Layton. "Cyclization of ′-(2-Aminophenyl)acetohydrazide." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-00690.

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Conference papers on the topic "Acetohydrazide"

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Ananda, S., V. Keerthikumara, N. R. Bhavya, et al. "Computational and experimental studies of nonlinear optical properties of acetohydrazide derivative." In 66TH DAE SOLID STATE PHYSICS SYMPOSIUM. AIP Publishing, 2024. http://dx.doi.org/10.1063/5.0178383.

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Rajkumar, M., Jessie Fernando, K. Senthil Kannan, et al. "Enactment by computational-structural and by the experimental studies of 2-hydroxyimino-2-(pyridin-2-yl)-N′-[1-(pyridin-2-yl) ethylidene] acetohydrazide – HIPYPYEAH crystalline specimen." In THE 8TH ANNUAL INTERNATIONAL SEMINAR ON TRENDS IN SCIENCE AND SCIENCE EDUCATION (AISTSSE) 2021. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0108293.

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Journal articles
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