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Journal articles on the topic 'Aryloxy Derivatives'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Wang, Wen Bin, Dan Liu, Dan Wei Pi, Quan Bin Liao, and Ming Guo Liu. "Microwave-Assisted Parallel Synthesis and Antioxidant Activity of Aryloxy-Acetyl Ferrocenes Derivatives." Advanced Materials Research 781-784 (September 2013): 1085–88. http://dx.doi.org/10.4028/www.scientific.net/amr.781-784.1085.

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Seven novel aryloxy-acetyl ferrocene derivatives were parallel synthesized under microwave irradiation conditions from chloroacetyl ferrocenes and substituted phenols with the aim of obtaining potential antioxidant agents. The target compounds were identified by IR, 1H NMR, MS and elemental analysis, and their antioxidant assays indicated that all the aryloxy-acetyl ferrocenes had certain effect on eliminating 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical. Their antioxidation activity significantly improved when rising the temperature until the temperature was 35°C. The structure-activity relat

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2

Amankulova, Dinara, Gulzat Berganayeva, Bates Kudaibergenova, Dinara Zhetpisbay, Ayshagul Sharipova, and Moldyr Dyusebaeva. "Recent Advances in the Synthesis and Applications of m-Aryloxy Phenols." Molecules 28, no. 6 (2023): 2657. http://dx.doi.org/10.3390/molecules28062657.

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Since phenol derivatives have high potential as building blocks for the synthesis of bioactive natural products and conducting polymers, many synthesis methods have been invented. In recent years, innovative synthetic methods have been developed for the preparation of m-aryloxy phenols, which has allowed for the preparation of complex m-aryloxy phenols with functional groups, such as esters, nitriles, and halogens, that impart specific properties of these compounds. This review provides an overview of recent advances in synthetic strategies for m-aryloxy phenols and their potential biological

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3

Zaidi, M. G. H., Seema Zaidi, and I. P. Pandey. "Synthesis and Screening of Substituted Thiadiazoles Against Gleophyllum Straitum." E-Journal of Chemistry 1, no. 3 (2004): 184–88. http://dx.doi.org/10.1155/2004/248431.

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Cyclocondensation of a series of substituted phenoxy methylene carboxylic acids with thiosemoicarbazides afforded 2-Amino-5-Aryloxy Methylene –1,3,4 Thiadiazoles (Ia-Ie). The later were subsequently condensed with different phenoxymethylene carboxylic acid chlorides into 2- Aryloxy Methyleneamido-5-Aryloxy Methylene–1,3,4-Thiadiazoloyl Amides. The wood preservation efficiency of the both class of compounds was evaluated against a wood rotting fungusGleophyllum Straitumat different concentrations using food poison technique. In general phenoxy derivatives have shown more control over the growth

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4

MANISH, PUROHIT, and K. SRIVASTAVA SANTOSH. "Synthesis and Screening of Antimicrobial and Anti-inflammatory Activities of Aryloxy Derivatives of Benzimidazoles." Journal of Indian Chemical Society Vol. 68, Mar 1991 (1991): 163–65. https://doi.org/10.5281/zenodo.6138259.

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Department of Chemistry, Doctor Harisingb Gour Vishwavldyalaya, Sagar-470 003 <em>Manuscript received 3 August 1990, revised 29 January 1991, accepted 15 February 1991</em> Synthesis and Screening of Antimicrobial and Anti-inflammatory Activities of Aryloxy Derivatives of Benzimidazoles 

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5

Vázquez, Karina, Christian Espinosa-Bustos, Jorge Soto-Delgado, et al. "New aryloxy-quinone derivatives as potential anti-Chagasic agents: synthesis, trypanosomicidal activity, electrochemical properties, pharmacophore elucidation and 3D-QSAR analysis." RSC Advances 5, no. 80 (2015): 65153–66. http://dx.doi.org/10.1039/c5ra10122k.

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A set of new aryloxy-quinones were synthesized and evaluated in vitro against the epimastigote form of Trypanosoma cruzi and their unspecific cytotoxicity was tested on murine macrophages J-774 cells.

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6

Sharma, Neeraj, B. S. Golen, R. K. Mahajan, and S. C. Chaudhry. "Synthesis and characterization of aryloxy derivatives of triorganoarsenic(V)." Polyhedron 10, no. 8 (1991): 789–91. http://dx.doi.org/10.1016/s0277-5387(00)86109-4.

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7

Yang, Ji-Chun, Miao Li, Qiao Wu, Chang-Ling Liu, and Xiu-Hui Chang. "Design, synthesis and insecticidal evaluation of aryloxy dihalopropene derivatives." Bioorganic & Medicinal Chemistry 24, no. 3 (2016): 383–90. http://dx.doi.org/10.1016/j.bmc.2015.09.030.

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8

Phakhodee, Wong, Nittaya Wiriya, Mookda Pattarawarapan, Saranphong Yimklan та Surat Hongsibsong. "Phosphonium-Mediated Synthesis of a New Class of Indoloquinazoline Derivatives Bearing a C-12 Aryloxy Ester or Spiro-γ-lactone". Synthesis 54, № 08 (2021): 2070–80. http://dx.doi.org/10.1055/a-1707-2924.

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AbstractIndoloquinazolines functionalized at C-12, which are structural analogs of the natural alkaloid cephalanthrin B, are readily constructed via Ph3P/I2-mediated one-pot reactions of isatins with aromatic alcohols. In the presence of excess phenols, the C-12 aryloxy ester products are obtained in moderate to good yields under mild conditions. Moreover, fused bicyclic hydroxyaryl derivatives such as 8-hydroxyquinoline give rise to novel C-12 spiro-γ-lactone derivatives. A reactive iminium cation species derived from dehydration of the C-12 hydroxy ester precursor is proposed as the transien

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9

Litvinov, Vasilii A., and Lyubov S. Klimenko. "Synthesis and studying the properties of photochromic materials based on derivatives of anthraquinone." Yugra State University Bulletin 12, no. 3 (2016): 12–19. http://dx.doi.org/10.17816/byusu201612312-19.

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Objects of the study are derivatives of 1-p-t-butyl-phenoxy-9,10-anthraquinone with the various substituents in the position 2 and 4. As a result new anthraquinone derivatives have been obtained and the comparative study of their photochromic properties in solutions and polymer layers have been realized. The direct dependence of photographic characteristics of samples on chemical structure and conditions of thermal treatment was established. Tests have shown that the acylaminoderivatives of 1-aryloxy-9, 10-anthra-quinone synthesized can be used as light sensitive components of photochromic mat

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10

Fan, Tao, Yan Liu, Caina Jiang, Yanli Xu, and Yanyan Chen. "A metal-free radical cascade reaction of phosphine oxides with 2-aryloxy phenylacetylenes to synthesize diphosphonyl xanthene derivatives." Organic & Biomolecular Chemistry 19, no. 30 (2021): 6609–12. http://dx.doi.org/10.1039/d1ob01045j.

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A cascade reaction of 2-aryloxy phenylacetylenes with phosphine oxides to provide diphosphonyl xanthenes promoted by K<sub>2</sub>S<sub>2</sub>O<sub>8</sub> was developed. This reaction features transition metal-free and mild conditions, simple operation and good yields.

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11

Tudose, Madalina, Florin Badea, Miron Caproiu, et al. "New N-aryloxy-phthalimide derivatives. Synthesis, physico-chemical properties, and QSPR studies." Open Chemistry 8, no. 4 (2010): 789–96. http://dx.doi.org/10.2478/s11532-010-0063-6.

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AbstractStarting from N-hydroxyphthalimide 1 and the reactive fluoro- or chloro-nitroaryl derivatives 2, 3 and 4a-e (2-chloro-3,5-dinitropyridine; 3, NBD-chloride; 4a, 1-fluoro-2,4-dinitrobenzene; 4b, picryl chloride; 4c, 4-chloro-3,5-dinitrobenzotrifluoride; 4d, 2-chloro-3,5- dinitrobenzotrifluoride; 4e, 4-chloro-3,5-dinitrobenzoic acid) the corresponding N-(2-nitroaryloxy)-phthalimide derivatives 5a-e, or 6 and 7 were obtained and characterized by IR, UV-Vis 1H-NMR and 13C-NMR spectroscopy. The TLC behavior and the hydrophobicity of these derivatives have been experimentally evaluated by RM0

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12

Bem, Marioara, Miron Caproiu, Dan Stoicescu, Titus Constantinescu, and Alexandru Balaban. "Synthesis of 4-aryloxy-7-nitrobenzofurazan derivatives from 4-chloro-7-nitrobenzofurazan and various phenoxide anions (including pharmaceuticals) in the presence of crown ethers." Open Chemistry 1, no. 3 (2003): 260–76. http://dx.doi.org/10.2478/bf02476228.

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Abstract4-Chloro-7-nitrobenzofurazan reacts by nucleophilic substitution with phenoxide anions derived from estriol (2c), ethynylestradiol (2d), phenol (3e), guaiacol (3f), 2,6-dimethoxyphenol (3g), eugenol (3h), isoeugenol (3i), the cytostatic Etoposide (4), and Reichardt’s betaine (5) in the presence of crown ethers affording the corresponding 4-aryloxy-7-nitrobenzofurazan derivatives 6c, 6d, 7e-7i, 8, and 9. The structure of these compounds was confirmed by NMR spectra. Hydrophobicity/hydrophilicity parameters were investigated by reverse phase thin-layer chromatography.

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13

Mamedbeili, E. G., I. A. Dzhafarov, K. A. Kochetkov, T. G. Kyazimova, and N. D. Kagramanov. "Synthesis of dialkylaminomethoxy derivatives of 3-aryloxy-1-(ethylsulfanyl)propanes." Russian Journal of Organic Chemistry 46, no. 2 (2010): 198–201. http://dx.doi.org/10.1134/s1070428010020090.

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14

Arora, Vishal, Manikrao M. Salunkhe, Neelima Sinha, Rakesh K. Sinha, and Sanjay Jain. "Synthesis and antibacterial activity of some aryloxy/thioaryloxy oxazolidinone derivatives." Bioorganic & Medicinal Chemistry Letters 14, no. 18 (2004): 4647–50. http://dx.doi.org/10.1016/j.bmcl.2004.06.096.

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15

Espinosa‐Bustos, Christian, Karina Vázquez, Javier Varela, et al. "New aryloxy‐quinone derivatives with promising activity on Trypanosoma cruzi." Archiv der Pharmazie 353, no. 1 (2019): 1900213. http://dx.doi.org/10.1002/ardp.201900213.

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16

Vairamani, M., K. V. Siva Kumar, and G. K. Viswanadha Rao. "Mass spectral study of derivatives of 2-aryloxy-2-methylpropanoicacids." Organic Mass Spectrometry 27, no. 2 (1992): 113–15. http://dx.doi.org/10.1002/oms.1210270208.

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17

Liu, Jianchao, Qingyun Ren, and Hongwu He. "Synthesis and Herbicidal Activity of 6-Alkoxy(aryloxy) Multisubstituted Pyridine Derivatives." Chinese Journal of Organic Chemistry 36, no. 9 (2016): 2225. http://dx.doi.org/10.6023/cjoc201603026.

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18

Cecchetti, Violetta, Arnaldo Fravolini, Fausto Schiaffella, Oriana Tabarrini, Giancarlo Bruni, and Giorgio Segre. "o-Chlorobenzenesulfonamidic derivatives of (aryloxy)propanolamines as .beta.-blocking/diuretic agents." Journal of Medicinal Chemistry 36, no. 1 (1993): 157–61. http://dx.doi.org/10.1021/jm00053a020.

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19

Vakarov, S. A., D. A. Gruzdev, G. L. Levit, V. P. Krasnov, V. N. Charushin, and O. N. Chupakhin. "Synthesis of enantiomerically pure 2-aryloxy carboxylic acids and their derivatives." Russian Chemical Reviews 88, no. 10 (2019): 1063–80. http://dx.doi.org/10.1070/rcr4893.

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20

Pazini, Alessandra, Luis Maqueira, Fabiano da Silveira Santos, et al. "Designing highly luminescent aryloxy-benzothiadiazole derivatives with aggregation-induced enhanced emission." Dyes and Pigments 178 (July 2020): 108377. http://dx.doi.org/10.1016/j.dyepig.2020.108377.

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21

Verrier, Charlie, Sébastien Carret, and Jean-François Poisson. "Asymmetric addition of aryloxy ethynyl lithium derivatives to N-sulfinyl imines." Monatshefte für Chemie - Chemical Monthly 144, no. 4 (2013): 455–60. http://dx.doi.org/10.1007/s00706-012-0907-1.

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22

Semenovykh, E. V., V. I. Pantsurkin, V. V. Novikova, T. F. Odegova, B. Ya Syropyatov, and M. I. Vakhrin. "Synthesis and antimicrobial activity of 2-aryloxy-N,N-diethylethanamine derivatives." Pharmaceutical Chemistry Journal 41, no. 4 (2007): 211–15. http://dx.doi.org/10.1007/s11094-007-0048-8.

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23

SHARMA, N., B. S. GOLEN, R. K. MAHAJAN, and S. C. CHAUDHRY. "ChemInform Abstract: Synthesis and Characterization of Aryloxy Derivatives of Triorganoarsenic(V)." ChemInform 22, no. 33 (2010): no. http://dx.doi.org/10.1002/chin.199133233.

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24

Vagin, Sergei I., and Michael Hanack. "Triazole-annulated phthalocyanines and benzoporphyrazines." Journal of Porphyrins and Phthalocyanines 10, no. 11 (2006): 1309–18. http://dx.doi.org/10.1142/s1088424606000685.

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The application of mono-triazole-annulated phthalocyanine and benzoporphyrazine complexes for the functional unsymmetrical modification of the macrocycle's periphery is discussed. The peculiarities of the synthesis of some metal complexes with aryloxy-substituted mono-triazole-annulated Pc are described. Alkylation by ω-alkenylbromide of the triazole ring in accordingly prepared novel mono-triazole-annulated phthalocyaninato nickel, as well as in mono-benzotriazole-annulated porphyrazinato zinc, is studied. The terminal double bond in the formed derivatives could be successfully converted into

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25

Klimenko, Lyubov S., Soltan Z. Kusov, Vladislav M. Vlasov, Elena N. Tchabueva, and Vladimir V. Boldyrev. "Solid-state photochemical reactions of 1-aryloxy(1-arylthio)-9,10-anthraquinone derivatives." Mendeleev Communications 16, no. 4 (2006): 224–25. http://dx.doi.org/10.1070/mc2006v016n04abeh002294.

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26

Bzowska, Agnieszka, Lucyna Magnowska, and Zygmunt Kazimierczuk. "Synthesis of 6-Aryloxy- and 6-Arylalkoxy-2-chloropurines and Their Interactions with Purine Nucleoside Phosphorylase from Escherichia coli." Zeitschrift für Naturforschung C 54, no. 12 (1999): 1055–67. http://dx.doi.org/10.1515/znc-1999-1210.

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The phase transfer method was applied to perform the nucleophilic substitution of 2,6- dichloropurines by modified arylalkyl alcohol or phenols. Since under these conditions only the 6-halogen is exchanged, this method gives 2-chloro-6-aryloxy- and 2-chloro-6-arylalkoxypurines. 2-Chloro-6-benzylthiopurine was synthesized by alkylation of 2-chloro-6-thiopurine with benzyl bromide. The stereoisomers of 2-chloro-6-(1-phenyl-1-ethoxy)purine were obtained from R- and S-enantiomers of sec.-phenylethylalcohol and 2,6-dichloropurine. All derivatives were tested for inhibition with purified hexameric E

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27

Kumar, Ashwini. "Fungicidal Activity of Novel Synthesized 2-(N-Aryloxy Acetyl)-5-(2'-Hydroxy Phenyl)-1, 3, 4-Oxadiazole." Journal of Advances in Science and Technology 21, no. 2 (2024): 212–18. https://doi.org/10.29070/hm0s4h11.

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After a novel set of 2-(N-aryloxy acetyl)-5-(2'-hydroxy phenyl)-1,3,4-oxadiazole derivatives were created, their fungicidal ability was evaluated. A mild condensation reaction of salicylic acid hydrazide with various aryloxyacetic acid chlorides produced the necessary heterocyclic molecules. The compounds' in vitro antifungal efficacy against a panel of phytopathogenic fungi, including Aspergillus niger, Rhizoctonia solani, and Fusarium oxysporum, was evaluated using the poisoned food technique. Numerous substances had significant inhibitory effects, with certain modifications enhancing the fu

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28

Kobek, Klaus, Manfred Focke, and K. Lichtenthaler Botanisches. "Fatty-acid biosynthesis and acetyl-coa carboxylase as a target of diclofop, fenoxaprop and other aryloxy-phenoxy-propionic acid herbicides." Zeitschrift für Naturforschung C 43, no. 1-2 (1988): 47–54. http://dx.doi.org/10.1515/znc-1988-1-212.

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The effect of the herbicides and aryloxy-phenoxy-propionic acid derivatives diclofop, fenoxaprop, fluazifop and haloxyfop and their ethyl, methyl or butyl esters on the de novo fatty-acid biosynthesis of isolated chloroplasts was investigated with intact chloroplasts isolated from sensitive grasses (Poaceae) and tolerant dicotyledonous plants (Pisum, Spinacia). The 4 herbicides (free-acid form) block the de novo fatty-acid biosynthesis ([2-14C]acetate incorporation into the total fatty-acid fraction) of the sensitive Avena chloroplasts in a dose-dependent manner. The I50- values (a 50% inhibit

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29

Aruna, G., Ravindra Kulkarni, Baswaraj Machaa, Malathi Jojula, Shravan Gunda, and G. Achaiah. "Design, Synthesis and Evaluation of Aryloxybenzylidene Hydrazinyl-Benzoxazoles/Benzothiazoles Analogs as Antimycobacterial Agents." Asian Journal of Organic & Medicinal Chemistry 5, no. 3 (2020): 185–91. http://dx.doi.org/10.14233/ajomc.2020.ajomc-p272.

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Substituted 2-(2-(4-aryloxybenzylidene)hydrazinyl)benzothiazole/benzoxazoles series were designed through molecular hybridization and synthesized in condensation reaction of hydrazinylbenzothiazole/ benzoxazole with substituted aryloxy benzaldehydes. All the synthesized compounds were assigned structure based on spectral data and were evaluated for antimycobacterial activity. Among both benzothiazole and benzoxazole derivatives, the compounds 8f and 9e were found to show most potent antitubercular activity with MIC value of 0.89 and 0.92 μM which are on a par with those of standard antitubercu

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30

Verrier, Charlie, Sebastien Carret, and Jean-Francois Poisson. "ChemInform Abstract: Asymmetric Addition of Aryloxy Ethynyl Lithium Derivatives to N-Sulfinyl Imines." ChemInform 44, no. 32 (2013): no. http://dx.doi.org/10.1002/chin.201332088.

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31

M., L. SHARMA, K. TALWAR K., and DUGGAL REEMA. "Synthesis of Quaternary Salts of Ammonia from Phenols and their Plant Growth Retardant Activity." Journal of Indian Chemical Society Vol. 75, Jun 1998 (1998): 381–83. https://doi.org/10.5281/zenodo.5937597.

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Department of Chemistry, Punjab Agricultural University, Ludhiana-141 004 <em>Manuscript received 28 January 1997, revised 21 October 1997, accepted 24 November 1997</em> Different phenols, viz. β-naphthol, <em>p</em>-chlorophenol, p-cresol and m-nitrophenol have been converted into (3-diethylamino-2- hydroxypropyloxy) derivatives (4a-d) through the formation of glycidyl ethers (2a-d and 3a-d). <em>m</em>-Nitrophenol and <em>p</em>-chlorophenol have been converted to 2-aryloxy-<em>N,N</em>-diethylaminoethanes (8e,f) through the formation of bromoethers (7e,f). 1,3-Bis(2- diethylaminocthox

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32

Wang, Hong-Mei, Tian-Shuai Wang, Sheng-Jie He, Zong-Yun Chen, and Yang-Gen Hu. "An efficient synthesis of 3-alkyl-2-diversity-substituted benzofuro[3,2-d]pyrimidin-4(3H)-one derivatives." Journal of Chemical Research 43, no. 5-6 (2019): 201–4. http://dx.doi.org/10.1177/1747519819858734.

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Benzofuro[3,2- d]pyrimidine derivatives are prepared using aza-Wittig reactions of iminophosphoranes with n-butyl isocyanate at 40–50 °C to give carbodiimide intermediates, which are reacted with nitrogen-oxygen-containing nucleophiles to give 3-alkyl-2-amino (aryloxy/alkoxy)-benzofuro[3,2- d]pyrimidin-4(3 H)-ones in satisfactory yields in the presence of a catalytic amount of sodium ethoxide or K2CO3. The iminophosphorane also reacts directly with excess carbon disulfide, followed by n-propylamine; further reaction with alkyl halides or halogenated aliphatic esters in the presence of anhydrou

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33

BERINDE, ZOITA-MARIOARA. "A QSPR study of hydrophobicity of phenols and 2-(aryloxy-α-acetyl)-phenoxathiin derivatives using the topological index ZEP". Creative Mathematics and Informatics 22, № 1 (2013): 33–40. http://dx.doi.org/10.37193/cmi.2013.01.01.

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The molecular hydrophobicity (RMO) of several newly synthesized phenoxathiin derivatives and of phenols with congeneric structures have been recently correlated with some simple physico-chemical calculated parameters of compounds: the water solubility (log Sw); the partition coefficient (log P); the Gibbs energy of formation (∆Gf ), and the aromaticity index (HOMA) [Beteringhe, A., Radutiu, A. C., Constantinescu, T., Patron, L. and Balaban, A. T., Quantitative Structure-Property Relationship (QSPR) study of the hydrophobicity of phenols and 2-(aryloxy-α-acetyl)- phenoxathiin derivatives, Rev.

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34

Adamczewski, Kazimierz, Roman Kierzek, and Kinga Matysiak. "Multiple resistance to acetolactate synthase (ALS)- and acetyl-coenzyme A carboxylase (ACCase)-inhibiting herbicides in black-grass (Alopecurus myosuroides Huds.) populations from Poland." Journal of Plant Protection Research 56, no. 4 (2016): 402–10. http://dx.doi.org/10.1515/jppr-2016-0059.

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AbstractAlopecurus myosuroides seeds were sampled from 32 winter wheat fields from 2010 to 2014. Resistance to herbicides was detected in 17 A. myosuroides populations. In addition to single resistance to herbicides, cross-resistance and multiple resistance to acetolactate synthase (ALS)- and acetyl-coenzyme A carboxylase (ACCase)-inhibiting herbicides were found. Application of sulfometuron and imazapyr was unable to control some of the resistant biotypes in this study. This result implies that resistance in these populations is due to a target site mechanism. The A. myosuroides biotypes resi

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35

Durmuş, Mahmut, and Tebello Nyokong. "Synthesis, photophysical and photochemical properties of aryloxy tetra-substituted gallium and indium phthalocyanine derivatives." Tetrahedron 63, no. 6 (2007): 1385–94. http://dx.doi.org/10.1016/j.tet.2006.11.089.

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36

Kusumi, Kensuke, Koji Shinozaki, Toshiya Kanaji, et al. "Discovery of novel S1P2 antagonists. Part 1: Discovery of 1,3-bis(aryloxy)benzene derivatives." Bioorganic & Medicinal Chemistry Letters 25, no. 7 (2015): 1479–82. http://dx.doi.org/10.1016/j.bmcl.2015.02.029.

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37

Walsh, David A., Ying Ho Chen, Jerry B. Green, Joseph C. Nolan, and John M. Yanni. "The synthesis and antiallergy activity of 1-(aryloxy)-4-(4-arylpiperazinyl)-2-butanol derivatives." Journal of Medicinal Chemistry 33, no. 6 (1990): 1823–27. http://dx.doi.org/10.1021/jm00168a044.

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38

Piplani, Poonam, Ruchi Malik, Bhavneet Kaur, and Anuradha Kaplish. "Synthesis and pharmacological evaluation of some new naphthol derived aryloxy derivatives as cognition enhancers." Medicinal Chemistry Research 21, no. 8 (2011): 1771–79. http://dx.doi.org/10.1007/s00044-011-9686-1.

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39

Dai, Lin-Lin, Dong-Dong Li, Xiu-Mei Zhao, Shuang Zhi, Hong-Sheng Shen, and Zi-Bo Yang. "Synthesis and Antitumor Effect of Sophoridine Derivatives Bearing an Acyclic Aryloxy Phosphoramidate Mustard Functionality." Journal of Heterocyclic Chemistry 56, no. 2 (2018): 417–25. http://dx.doi.org/10.1002/jhet.3413.

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40

Shen, Changchao, Wenwei Tang, Dongqiang Zeng, Hongle Xu, Wangcang Su, and Renhai Wu. "Isoxadifen-Ethyl Derivatives Protect Rice from Fenoxaprop-P-Ethyl–associated Injury during the Control of Weedy Rice." Weed Science 65, no. 5 (2017): 579–87. http://dx.doi.org/10.1017/wsc.2017.27.

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Fenoxaprop-P-ethyl, a phenoxy herbicide of the aryloxy–phenoxy–propionic acid group, had a strong control effect when applied POST to weedy rice in this study, with the effective concentrations of 294 μM and 218 μM of herbicide causing 50% inhibition (IC50) in plant height and fresh weight values, respectively. However, fenoxaprop-P-ethyl caused phytotoxicity in cultivated rice. Isoxadifen-ethyl, a widely used herbicide safener in rice, can decrease the phytotoxicity caused by fenoxaprop-P-ethyl. Owing to the extremely similar morphological features and physiological properties of weedy and cu

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41

Soltani Hekmat, Ava, Mojtaba Farjam, Kazem Javanmardi, Somayeh Behrouz, Elham Zarenezhad, and Mohammad Navid Soltani Rad. "Design, Synthesis and In Vivo Cardiovascular Evaluation of Some Novel Aryloxy Propanol Amino Acid Derivatives." ChemistrySelect 6, no. 47 (2021): 13595–600. http://dx.doi.org/10.1002/slct.202101920.

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42

Huang, Jiulin, Si-Ying Xiang, Min Lv, et al. "14-Formyl-15-aryloxy/methoxymatrine and 14-Aryloxymethylidenyl-matrine Derivatives as Anti-HIV-1 Agents." Medicinal Chemistry 14, no. 3 (2018): 249–52. http://dx.doi.org/10.2174/1573406413666171002120310.

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Zhao, Shuo, Jun-Jun Huang, Xiuyun Sun, et al. "(1-aryloxy-2-hydroxypropyl)-phenylpiperazine derivatives suppress Candida albicans virulence by interfering with morphological transition." Microbial Biotechnology 11, no. 6 (2018): 1080–89. http://dx.doi.org/10.1111/1751-7915.13307.

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Li, Feng, Xiao-Min Li, Dekuan Sheng, et al. "Discovery and preliminary SAR of 14-aryloxy-andrographolide derivatives as antibacterial agents with immunosuppressant activity." RSC Advances 8, no. 17 (2018): 9440–56. http://dx.doi.org/10.1039/c8ra01063c.

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6b17 and 9b are active against 3 tested bacteria while they block IL-6/STAT3, TLR4/NF-κB and TNF-α/NF-κB pathways. 7b1 and 8b1 are selectively active against E. faecalis but 7b1 selectively blocks TNF-α/NF-κB pathway and 8b1 selectively blocks TLR4/NF-κB pathway.

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Guan, Aiying, Changling Liu, Wei Chen, et al. "Design, Synthesis, and Structure–Activity Relationship of New Pyrimidinamine Derivatives Containing an Aryloxy Pyridine Moiety." Journal of Agricultural and Food Chemistry 65, no. 6 (2017): 1272–80. http://dx.doi.org/10.1021/acs.jafc.6b05580.

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Citterio, Attilio, Daniele Fancelli, Claudia Finzi, Luca Pesce, and Roberto Santi. "Manganese(III) acetate-induced cyclization of .alpha.-(arylalkyl) and .alpha.-(aryloxy)alkyl .beta.-dicarbonyl derivatives." Journal of Organic Chemistry 54, no. 11 (1989): 2713–18. http://dx.doi.org/10.1021/jo00272a047.

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Stankyavichene, L. M. M., D. I. L. Raizhene, V. K. Vizas, A. P. Stankyavichyus, and P. B. Terent'ev. "Synthesis and study of quaternary ammonium derivatives of d1-1-aryloxy-2-hydroxy-3-aminopropanes." Pharmaceutical Chemistry Journal 20, no. 5 (1986): 323–28. http://dx.doi.org/10.1007/bf00758612.

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Zajdel, Paweł, Vittorio Canale, Anna Partyka, et al. "Arylsulfonamide derivatives of (aryloxy)ethylpiperidines as selective 5-HT7 receptor antagonists and their psychotropic properties." MedChemComm 6, no. 7 (2015): 1272–77. http://dx.doi.org/10.1039/c5md00166h.

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Klimenko, L. S., I. Ya Mainagashev, and E. P. Fokin. "Photochemical and thermal transformations of diazo derivatives of 1-aryloxy- and 1-arylthio-2-aminoanthraquinones." Bulletin of the Russian Academy of Sciences Division of Chemical Science 41, no. 3 (1992): 459–61. http://dx.doi.org/10.1007/bf00863063.

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Chaves-Carballo, Katherine, Guy V. Lamoureux, Alice L. Perez, Alexandre Bella Cruz, and Valdir Cechinel Filho. "Novel one-pot synthesis of a library of 2-aryloxy-1,4-naphthoquinone derivatives. Determination of antifungal and antibacterial activity." RSC Advances 12, no. 29 (2022): 18507–23. http://dx.doi.org/10.1039/d2ra01814d.

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The development of new antibiotics and inexpensive antifungals is an important field of research. Based on the privileged pharmacophore of lawsone, a series of phenolic ether derivatives of 1,4-naphthoquinone were synthesized easily in one step in reasonable yields.

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