Relevant bibliographies by topics / Amino-oxy compounds

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Academic literature on the topic 'Amino-oxy compounds'

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

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Journal articles on the topic "Amino-oxy compounds"

1

Laddi, U. V., and S. R. Desai. "SYNTHESIS AND ANTIMICROBIAL ACTIVITY OF SOME NEW 1,3,4- OXADIAZOLES, 1,2,4-TRIAZOLES AND 1,3,4-THIADIAZOLES." INDIAN DRUGS 53, no. 06 (2016): 18–23. http://dx.doi.org/10.53879/id.53.06.10489.

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Some new 5-[(((α-phenyl/methyl)benzylidene)amino)oxy]methyl/ethyl-2-[4-(substituted aryl)/allyl)] amino-1,3,4-oxadiazoles (4a-p), 3-[(((α-phenyl/methyl)- benzylidene) amino)oxy]methyl/ethyl-4-(4- substitutedaryl)/allyl-5-mercapto-1,2,4-triazoles (5a-p) and 5-[(((α-phenyl/methyl)-benzylidene)amino) oxy]- methyl/ethyl-2-[4-(substituted aryl)/allyl)]amino-1,3,4-thiadiazoles (6a-p) were prepared starting from α/β-[((α-(phenyl/methyl)benzylidene)amino)oxy acetic/propionic acid hydrazides (1a-d). The structures of all the compounds have been established by elemental and spectral (IR, 1HNMR and mass)
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2

Laddi, U. V., and S. Desai. "SOME NEW 1,3,4-OXADIAZOLES AS ANTIMICROBIAL AGENTS." INDIAN DRUGS 53, no. 02 (2016): 15–18. http://dx.doi.org/10.53879/id.53.02.10490.

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Some new 5-[(((α-phenyl/methyl)benzylidene)amino)oxy]methyl/ethyl-2-amino/4-substituted aryl/ aryloxymethylarmercapto/piperidino/ morpholino-1,3,4-oxadiazoles (2a-d–5a-d) with biologically active biostere methyelne amino oxy methyl/ethyl moiety, were prepared starting from α/β-[((α-(phenyl/methyl) benzylidene)amino)oxy acetic/propionic acid hydrazides (1a-d). The structures of the compounds have been characterised by elemental and spectral (IR, 1HNMR and mass) analysis. All the newly synthesised compounds have been screened for their antimicrobial activity by cup plate method, against Escheric
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3

Tahira, Banu, Rajora Sonal, Khatri Dilip, and L. Talesara G. "Synthesis of some isoindole-1,3-dione and amino-oxyalkyl derivatives of benzimidazole." Journal of Indian Chemical Society Vol. 77, Jun 2000 (2000): 300–301. https://doi.org/10.5281/zenodo.5869883.

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Department of Chemistry, College of Science, Sukhadia University, Udaipur-313 001, India <em>Manuscript received 3 May 1999, revised 14 October 1999, accepted 23 February 2000</em> 2-(Bromoalkoxy)-1<em>H</em>-isoindole-1,3-diones are condensed with benzimidazole and its derivatives to give 2-[(benzimidazole-1-yl)-alkoxy]- 1<em>H</em>-isoindole-1,3-diones. Hydrolysis under acidic conditions gives the corresponding amino-oxy compounds.
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4

Mahdi, Omar, Hanaa Salih, and Abdullah Kshash. "Design, Synthesis of a Novel Banana-Shaped Compounds via Esterification." Diyala Journal For Pure Science 17, no. 4 (2021): 81–92. http://dx.doi.org/10.24237/djps.17.04.568c.

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Schiff's Bases were synthesized from the reaction of p-amino benzoic acid and alkoxybenzaldehyde in absolute ethanol and reacted with (E)-3-((4-hydroxybenzylidene) amino) phenol used DCC (N,N'-Dicyclocarbodiimide) and DAMP (4-(Dimethylamino) pyridine ) to 3-(((E)-4-((4-(((E)-4 alkoxy benzylidene) amino) benzoyl) oxy) benzylidene) amino) phenyl4- (E)- 4-alkoxy benzyli dene ) amino) benzoate. The structures of the products were confirmed by their melting points, FT-IR, 1HNMR spectra.
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5

Makarasen, Arthit, Mayuso Kuno, Suwicha Patnin, et al. "Molecular Docking Studies and Synthesis of Amino-oxy-diarylquinoline Derivatives as Potent Non-nucleoside HIV-1 Reverse Transcriptase Inhibitors." Drug Research 69, no. 12 (2019): 671–82. http://dx.doi.org/10.1055/a-0968-1150.

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AbstractIn this study, amino-oxy-diarylquinolines were designed using structure-guided molecular hybridization strategy and fusing of the pharmacophore templates of nevirapine (NVP), efavirenz (EFV), etravirine (ETV, TMC125) and rilpivirine (RPV, TMC278). The anti-HIV-1 reverse transcriptase (RT) activity was evaluated using standard ELISA method, and the cytotoxic activity was performed using MTT and XTT assays. The primary bioassay results indicated that 2-amino-4-oxy-diarylquinolines possess moderate inhibitory properties against HIV-1 RT. Molecular docking results showed that 2-amino-4-oxy
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6

Egorova, Irina, Elena Maltseva, and Lyudmila Pinchuk. "Phytochemical study of Glycyrrhiza pallidiflora Maxim." BIO Web of Conferences 128 (2024): 00023. http://dx.doi.org/10.1051/bioconf/202412800023.

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This article presents the results of the primary phytochemical study of Glycyrrhiza pallidiflora Maxim. introduced in the southeast of Western Siberia. The qualitative and quantitative composition of several primary and secondary metabolites in underground and aboveground organs of the plant were studied in different years of introduction and vegetation period. The presence of triterpene saponins, coumarins, chromones, chalcones, aurones, 5-oxy-flavones, 5-oxy-flavonols, flavan-3-ols, and proanthocyanidins was determined. The total content of phenolic compounds in the grass reached 2.83±0.22%
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7

Khalefa, Omar S. "New Schiff base compounds with benzene moiety: FT-IR, 1H and 13C NMR Spectroscopy (1D) studies." BASRA JOURNAL OF SCIENCE 38, no. 1 (2020): 98–110. http://dx.doi.org/10.29072/basjs.20200105.

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New Schiff bases compounds containing benzene moiety has been synthesized from reaction between (4-(((4-(Alkyloxy) benzylidene) amino) methyl) phenyl)methan amine and 4-((6-bromohexyl) oxy)benzaldehyde or 4-(4-bromobutoxy)benzaldehyde. FT-IR of these compounds have been studied. The complete 1H and 13C NMR assignment of these compounds has been obtained using one-dimensional NMR techniques including 1H and 13C experiments. The data deduced from this study show that the alkyl chain and the phenyl rings are in different planes compared to the benzene ring.
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8

Khalefa, Omar S. "New Schiff base compounds with benzene moiety: FT-IR, 1H and 13C NMR Spectroscopy (1D) studies." BASRA JOURNAL OF SCIENCE 38, no. 1 (2020): 98–110. http://dx.doi.org/10.29072/basjs.20200108.

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New Schiff bases compounds containing benzene moiety has been synthesized from reaction between (4-(((4-(Alkyloxy) benzylidene) amino) methyl) phenyl)methan amine and 4-((6-bromohexyl) oxy)benzaldehyde or 4-(4-bromobutoxy)benzaldehyde. FT-IR of these compounds have been studied. The complete 1H and 13C NMR assignment of these compounds has been obtained using one-dimensional NMR techniques including 1H and 13C experiments. The data deduced from this study show that the alkyl chain and the phenyl rings are in different planes compared to the benzene ring.
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9

Vijay, Kumar Salvi, Pemawat Gangotri, Bapna Archita, and L. Talesara G. "Synthesis, characterization and antimicrobial activity of substituted 3-(phthalazine-1-ylamino)alkanoic acid containing imidoxy moiety." Journal of Indian Chemical Society Vol. 86, May 2009 (2009): 491–97. https://doi.org/10.5281/zenodo.5810168.

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Synthetic Organic Chemistry Research Laboratory, Department of Chemistry, M. L. Sukhadia University, Udaipur-313 001, Rajasthan, India <em>E-mail</em> : gtalesara@yahoo.com <em>Manuscript received 12 May 2008, revised 16 January 2009, accepted 20 January 2009</em> Hydrozinolysis of phthalyl derivatives of amino acid la-c afforded [(4-oxo-3,4-dihydrophthalazine-1- yl)amino]substituted acetic acid 2a-c, which on reaction with POCI<sub>3</sub>/PCI<sub>5</sub> gave ((4-chlorophahalazine-1-yl)amino]substituted acetic acid 3a-c. This when condensed with <em>N</em>-hydroxyphthalimide/ N-hydroxysuccin
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10

Sun, Guanghui, Weilian Xie, Hong Xiao, and Guohai Xu. "Controlled interpenetration of 44networks: syntheses and structures of two Cu3-cluster coordination polymers." Acta Crystallographica Section C Structural Chemistry 74, no. 11 (2018): 1540–46. http://dx.doi.org/10.1107/s2053229618014262.

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The reaction of copper nitrate and triethanolamine with benzene-1,4-dicarboxylic acid (bdcH2) or 4,4′-[1,4-phenylenebis(oxy)]dibenzoic acid (podaH2) leads to the formation of poly[bis(μ4-benzene-1,4-dicarboxylato-κ4O1:O1′:O4:O4)bis{μ2-[bis(2-hydroxyethyl)amino]ethanolato-κ4N,O,O′,O′′:κO}tricopper(II)], [Cu3(C8H4O4)2(C6H14NO3)2] or [Cu3(μ4-bdc)2(teaH2)2] (I), and poly[bis{μ4-4,4′-[1,4-phenylenebis(oxy)]dibenzoato-κ4O:O′:O′′:O′′}bis{μ2-[bis(2-hydroxyethyl)amino]ethanolato-κ4N,O,O′,O′′:κO}tricopper(II)], [Cu3(C20H12O6)2(C6H14NO3)2] or [Cu3(μ4-poda)2(teaH2)2], (II). The two representative compound
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Book chapters on the topic "Amino-oxy compounds"

1

Taber, Douglass F. "Oxidation of Organic Functional Groups." In Organic Synthesis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190646165.003.0008.

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Cancheng Guo of Hunan University devised (J. Org. Chem. 2014, 79, 2709) con­ditions for the oxidative cleavage of an alkyne 1 to the esters 2 and 3. Hirokazu Arimoto of Tohoku University found (Chem. Commun. 2014, 50, 2758) that IBX oxidized a primary alcohol 4 to the acid 5 one carbon shorter. David Milstein of the Weizmann Institute of Science uncovered (J. Am. Chem. Soc. 2014, 136, 2998) condi­tions for the direct oxidation of the cyclic amine 6 to the lactam 7, with concomitant evolution of H₂. Cyclic ene sulfonamides such as 9 are versatile synthetic intermediates. Henri Doucet of the Uni
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