Relevant bibliographies by topics / 4,5-dihydroisoxazole

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic '4,5-dihydroisoxazole'

Author: Grafiati
Published: 9 March 2023
Last updated: 31 July 2025

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Journal articles on the topic "4,5-dihydroisoxazole"

1

Pir, Meryem, Fatma Budak, and Kemal Metiner. "Determination of in vitro antifungal activity of dihydroisoxazole dimethanol compound against dermatophytes obtained from clinical isolates and design of some new dihydroisoxazole dimethanol compounds." International Journal of Chemistry and Technology 8, no. 1 (2024): 45–50. http://dx.doi.org/10.32571/ijct.1109476.

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In this study, the in vitro antifungal activity of (3-(4-chlorophenyl)-4,5-dihydroisoxazole-4,5-diyl) dimethanol compound (1) was investigated against two pathogenic fungi species (Trichophyton mentagrophytes and Microsporum canis) and important results were obtained. The difficulty of treating fungal diseases induced us to assess the antifungal properties of dihydroisoxazole dimethanol compound. The broth microdilution method was used to determine the minimum inhibitory concentration (MIC). The compound (1) showed an antifungal effect with MIC=12.5 µg ml-1 on M. canis and MIC=50 µg ml-1 on T.
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2

Samshuddin, S., Ray J. Butcher, Mehmet Akkurt, B. Narayana, and H. S. Yathirajan. "3,5-Bis(4-methoxyphenyl)-4,5-dihydroisoxazole." Acta Crystallographica Section E Structure Reports Online 67, no. 8 (2011): o1975—o1976. http://dx.doi.org/10.1107/s1600536811026833.

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3

Sangale, Shital S., Priyanka S. Kale, Rachana B. Lamkane, Ganga S. Gore, Priyanka B. Parekar, and Shivraj S. Shivpuje. "Synthesis of Novel Isoxazole Derivatives as Analgesic Agents by Using Eddy’s Hot Plate Method." South Asian Research Journal of Pharmaceutical Sciences 5, no. 01 (2023): 18–27. http://dx.doi.org/10.36346/sarjps.2023.v05i01.002.

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The Isoxazole ring system belongs to a much studied class of compound. In the last few decades, the chemistry of Isoxazoles and their fused heterocyclic derivatives have received considerable attention owing to their significant and effective biological activity. The present study aimed to design and synthesize novel derivatives of Isoxazole from 4-methoxy aniline gives N-(4-methoxyphenyl) acetamide which was hydrolysis with sodium hydroxide and treated aromatic aldehydes yields resultant compound N-(4-methoxyphenyl) 3-phenyl propanamide (BSM-IIIA-IIIJ). Title compound were synthesized and the
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4

Barluenga, Joseé, Vicente Gotor, and María José Iglesias. "Synthesis of 4,5-dihydroisoxazole and isoxazolin-5-ones." Journal of Heterocyclic Chemistry 29, no. 7 (1992): 1717–19. http://dx.doi.org/10.1002/jhet.5570290707.

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5

Chopra, Deepak, T. P. Mohan, and B. Vishalakshi. "5-(4-Fluoro-3-phenoxyphenyl)-3-phenyl-4,5-dihydroisoxazole." Acta Crystallographica Section E Structure Reports Online 62, no. 9 (2006): o3819—o3820. http://dx.doi.org/10.1107/s1600536806030807.

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6

Jeddeloh, Melissa R., Jason B. Holden, Dustin H. Nouri, and Mark J. Kurth. "A Library of 3-Aryl-4,5-dihydroisoxazole-5-carboxamides." Journal of Combinatorial Chemistry 9, no. 6 (2007): 1041–45. http://dx.doi.org/10.1021/cc700117a.

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7

Thirunarayanan, G., and V. Sathiyendiran. "Synthesis, Pharmacological and Insect Antifeedant Activities of some 3-(2-Naphthyl)-5-(Substituted Phenyl)-4,5-Dihydroisoxazoles." International Letters of Chemistry, Physics and Astronomy 49 (April 2015): 1–14. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.49.1.

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Totally thirty one 3,5-substituted aryl 4,5-dihydro isoxazole derivatives including 3-(2-naphthyl)-5-(substituted phenyl)-4,5-dihydroisoxazole have been synthesized by fly-ash:H2SO4 catalyzed cyclization of hydroxylamine hydrochloride and aryl chalcones under solvent-free conditions. The yields of the isoxazoles are more than 94%. The synthesized isoxazole were characterized by their physical constants and spectral data. The antimicrobial, antioxidant and insect antifeedant activities of the synthesized isoxazoles have been evaluated using a variety of bacterial and fungal species, DPPH radica
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8

Thirunarayanan, G., and V. Sathiyendiran. "Synthesis, Pharmacological and Insect Antifeedant Activities of some 3-(2-Naphthyl)-5-(Substituted Phenyl)-4,5-Dihydroisoxazoles." International Letters of Chemistry, Physics and Astronomy 49 (April 7, 2015): 1–14. http://dx.doi.org/10.56431/p-g0r04d.

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Totally thirty one 3,5-substituted aryl 4,5-dihydro isoxazole derivatives including 3-(2-naphthyl)-5-(substituted phenyl)-4,5-dihydroisoxazole have been synthesized by fly-ash:H2SO4 catalyzed cyclization of hydroxylamine hydrochloride and aryl chalcones under solvent-free conditions. The yields of the isoxazoles are more than 94%. The synthesized isoxazole were characterized by their physical constants and spectral data. The antimicrobial, antioxidant and insect antifeedant activities of the synthesized isoxazoles have been evaluated using a variety of bacterial and fungal species, DPPH radica
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9

Fernández, Rosario, José Lassaletta, Abel Ros, Eleuterio Alvarez, and Hansjörg Dietrich. "A Practical Synthesis of Enantiopure 4,5-Dihydroisoxazole-5-carboxylic Acids." Synlett 2005, no. 19 (2005): 2899–904. http://dx.doi.org/10.1055/s-2005-921894.

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10

Chopra, Deepak, T. P. Mohan, and B. Vishalakshi. "5-(4-Fluoro-3-phenoxyphenyl)-3-(4-methylphenyl)-4,5-dihydroisoxazole." Acta Crystallographica Section E Structure Reports Online 62, no. 8 (2006): o3547—o3548. http://dx.doi.org/10.1107/s1600536806028406.

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Dissertations / Theses on the topic "4,5-dihydroisoxazole"

1

Gallanti, M. "STEREOSELECTIVE SYNTHESIS OF A-AMINO ACIDS B-SUBSTITUTED WITH A 4,5-DIHYDROISOXAZOLE NUCLEUS AND OF TERTIARY AND QUATERNARY ALLYLSILANES." Doctoral thesis, Università degli Studi di Milano, 2012. http://hdl.handle.net/2434/168366.

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In the section A of the thesis is presented a stereoselective synthesis of b-hydroxy-a -amino acids b-substituted with a 4,5 dihydroisoxazole nucleus through an aldol type reaction between Schollkopf reagent and isoxazolynil aldehydes and ketones. In the section B is presented the preparation of allyl- or crotylsilane in high dr and er via the lithiation-borylation reaction of alkylcarbamates with silaboronates.The synthesis of quaternary allylsilane through a related strategy is also presented.
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Journal articles
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