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Relevant bibliographies by topics / -(4-methoxy)-1-phenylprop-2-en-1-one

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Academic literature on the topic '-(4-methoxy)-1-phenylprop-2-en-1-one'

Author: Grafiati

Published: 7 June 2025

Last updated: 2 August 2025

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Journal articles on the topic "-(4-methoxy)-1-phenylprop-2-en-1-one"

1

Asmau, Nasiru Hamza, and Kizito Igomu George. "Microwave Assisted Synthesis and Antimicrobial Screening of 3-(4-Methoxy)-1-Phenylprop-2-en-1-One." Pharmaceutical and Chemical Journal 3, no. 2 (2016): 300–303. https://doi.org/10.5281/zenodo.13754340.

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In an effort to develop novel antimicrobial agents, 3-(4-methoxy)-1-phenylprop-2-en-1-one was synthesized from acetophenone and methoxybenzaldehyde using the conventional Claisen-Schmidt condensation and microwave assisted methods. The conventional Claisen-Schmidt condensation afforded a yield of 35.29% in three hours. Whereas, the microwave assisted method gave 73.94% yield of 3-(4-methoxy)-1-phenylprop-2-en-1-one with two minutes. The synthesized 3-(4-methoxy)-1-phenylprop-2-en-1-one was characterized by means of Fourier transform Infrared (FTIR) spectroscopy, Shinoda’s test and meltin

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2

Betz, Richard, Thomas Gerber, Eric Hosten, S. Samshuddin, Badiadka Narayana, and Hemmige S. Yathirajan. "(E)-1-(4,4′′-Difluoro-5′-methoxy-1,1′:3′,1′′-terphenyl-4′-yl)-3-phenylprop-2-en-1-one." Acta Crystallographica Section E Structure Reports Online 67, no. 12 (2011): o3159—o3160. http://dx.doi.org/10.1107/s1600536811045375.

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3

Wang, Gao-Feng. "Synthesis and structural characterization of two copper(II) complexes with 3-(4-(1H-benzo[d]imidazol-1-yl)-4-methoxyphenyl)-1-phenylprop- 2-en-1-one ligands." Zeitschrift für Naturforschung B 70, no. 3 (2015): 165–69. http://dx.doi.org/10.1515/znb-2014-0197.

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AbstractThe synthesis of two new copper(II) complexes with benzimidazole type ligands, Cu(tta)2(L1)2 (1) and Cu(tta)2(L1) (2) (where L1 is 3-(4-(1H-benzo[d]imidazol-1-yl)-4-methoxy phenyl)-1-phenylprop-2-en-1-one; tta is 2-thenoyltrifluoroacetonate), are reported. Their structures have been characterized by infrared spectroscopy, elemental analyses and single-crystal X-ray diffraction. The copper(II) ion of 1 is in a distorted octahedral environment, while that of 2 is in a distorted square-pyramidal environment. In both cases, the donor atoms are provided by oxygen atoms of the tta ligands an

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4

Asgarova, Aytan R., Ali N. Khalilov, Ivan Brito, et al. "Hydrogen and halogen bonding in the haloetherification products in chalcone." Acta Crystallographica Section C Structural Chemistry 75, no. 3 (2019): 342–47. http://dx.doi.org/10.1107/s2053229619001025.

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Cooperative action of hydrogen and halogen bonding in the reaction of 3-(3,5-di-tert-butyl-4-hydroxyphenyl)-1-phenylprop-2-en-1-one with HCl or HBr in alcohol medium under microwave irradiation (20 W, 80 °C, 10 min) allows the isolation of the haloetherification products (2S,3S)-3-(3-tert-butyl-5-chloro-4-hydroxyphenyl)-2-chloro-3-ethoxy-1-phenylpropan-1-one, C21H24Cl2O3, (2S,3S)-2-bromo-3-(3-tert-butyl-5-bromo-4-hydroxyphenyl)-3-methoxy-1-phenylpropan-1-one, C20H22Br2O3, and (2S,3S)-2-bromo-3-(3-tert-butyl-5-bromo-4-hydroxyphenyl)-3-ethoxy-1-phenylpropan-1-one, C21H24Br2O3, in good yields. Bo

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5

Umapathi, Nalla, Pochampally Jalapathi, Matta Raghavender, and Bhookya Shankar. "Synthesis of (E)-1-(2,4-Bis((1-phenyl-1H-1,2,3-triazol-4-yl)methoxy)phenyl)- 3-phenylprop-2-en-1-one Derivatives and their Antimicrobial Activity." Asian Journal of Chemistry 33, no. 10 (2021): 2341–46. http://dx.doi.org/10.14233/ajchem.2021.23320.

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A new series of chalcone based bis 1,4-disubstituted 1,2,3-triazole heterocyclic molecules (6a-j) were synthesized via the reaction of 1-(2,4-bis((1-phenyl-1H-1,2,3-triazol-4-yl)methoxy)phenyl)ethanone (6a-e) with substituted benzaldehyde. All the molecules were characterized by IR, 1H and 13C NMR and MS spectra spectral data. Compounds 6a-j were evaluated for their antimicrobial effects using a broth disc diffusion method. The compounds were evaluated for their in vitro antimicrobial potential against Gram-positive (Micrococcus luteus, Methicillin-resistant Staphylococcus aureus, Bacillus sub

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6

MAROYI, ALFRED. "PHYTOCHEMICAL AND ETHNOPHARMACOLOGICAL REVIEW OF HETEROPYXIS NATALENSIS." Asian Journal of Pharmaceutical and Clinical Research, February 15, 2019, 8–15. http://dx.doi.org/10.22159/ajpcr.2019.v12i3.29375.

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The bark, leaves, roots, and twigs of Heteropyxis natalensis are widely used as herbal medicines in Southern Africa. The aim of this study was to review the phytochemical and ethnopharmacological properties of H. natalensis so as to provide baseline data required for evaluating the therapeutic potential of the species. Information on the botanical profile, medicinal uses, phytochemistry, and pharmacological properties of H. natalensis was undertaken using databases such as ScienceDirect, SciFinder, PubMed, Google Scholar, Medline, SCOPUS, EThOS, ProQuest, OATD, and open-thesis. Pre-electronic

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7

Turdybekov, Кoblandy M., Pernesh Zh Zhanymkhanova, Gulim K. Mukusheva, and Yurii V. Gatilov. "Synthesis and Spatial Structure of (E)-1-(2-(4-Bromobutoxy)- 6-Hydroxy-4-Methoxyphenyl-3-Phenylprop-2-en-1-one." Eurasian Journal of Chemistry, 2023. http://dx.doi.org/10.31489/2959-0663/2-23-2.

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(E)-1-(2-(4-bromobutoxy)-6-hydroxy-4-methoxyphenyl-3-phenylprop-2-en-1-one was synthesized from the pinostrobin molecule. The tetrahydropyran cycle was opened in acetone under heating (50–60 °C) mixtures of components for 16 hours in the presence of 3 moles of K2CO3 and 1,4-dibromobutane. The resulting sub-stance is a yellow powder of the composition C20H21BrO4, mp 83.7–86.6 °C. The structure of the obtained compound was established on the basis of the data of elemental analysis, IR and NMR spectra. As a result of X-ray diffraction analysis, it was found that the hydrogen atoms in the C8=C9 bo

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