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Journal articles on the topic 'Aryloxyacetic acids'

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Author: Grafiati
Published: 18 May 2024

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1

Berger, Michael, John D. Herszman, Yuji Kurimoto, Goswinus H. M. de Kruijff, Aaron Schüll, Sven Ruf, and Siegfried R. Waldvogel. "Metal-free electrochemical fluorodecarboxylation of aryloxyacetic acids to fluoromethyl aryl ethers." Chemical Science 11, no. 23 (2020): 6053–57. http://dx.doi.org/10.1039/d0sc02417a.

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2

Li, Zheng, Jin-Lan Yu, Jing-Ya Yang, Sheng-Yi Shi, and Xi-Cun Wang. "Polymer-supported Dichlorophosphate: A Recoverable New Reagent for Synthesis of 2-amino-1,3,4-thiadiazoles." Journal of Chemical Research 2005, no. 5 (May 2005): 341–43. http://dx.doi.org/10.3184/0308234054323913.

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Poly(ethylene glycol) (PEG) supported dichlorophosphate was efficiently used as a recoverable new dehydration reagent for rapid synthesis of 2-amino-5-substituted-1,3,4-thiadiazoles under microwave irradiation and solvent-free condition by reactions of thiosemicarbazide with aliphatic acids, benzoic acid, aryloxyacetic acids or furan-2-carboxylic acids.
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3

Abdel Hamid, Hamida M., El Sayed Ramadan, Mohamed Hagar, and El Sayed H. El Ashry. "Synthesis of Aryloxyacetic Acids, Esters, and Hydrazides Assisted by Microwave Irradiation." Synthetic Communications 34, no. 3 (December 31, 2004): 377–82. http://dx.doi.org/10.1081/scc-120027275.

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4

Leung, Joe C. T., and Glenn M. Sammis. "Radical Decarboxylative Fluorination of Aryloxyacetic Acids UsingN-Fluorobenzenesulfonimide and a Photosensitizer." European Journal of Organic Chemistry 2015, no. 10 (February 5, 2015): 2197–204. http://dx.doi.org/10.1002/ejoc.201500038.

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5

Villemin, Didier, and Mohamed Hammadi. "Environmentally Desirable Synthesis Without Use of Organic Solvent. Synthesis of Aryloxyacetic Acids." Synthetic Communications 26, no. 23 (December 1996): 4337–41. http://dx.doi.org/10.1080/00397919608003836.

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6

Raskil’dina, Gul’nara Z., Evgeniya A. Yakovenko, Luisa M. M. Mryasova, and Simon S. Zlotskii. "SYNTHESIS AND HERBICID ACTIVITY OF ARYLOXYACETIC ACIDS AND AMIDES OF ARYLOXY ACETIC ACIDS CONTAINING CYCLOACETAL FRAGMENT." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENIY KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 62, no. 1 (December 30, 2018): 91–97. http://dx.doi.org/10.6060/ivkkt.20196201.5753.

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The herbicidal activity of esters and amides based on commercially available phenoxy chlorides and 2,4-dichlorophenoxyacetic acids was studied. Esters of 2,2-methyl-4-hydroxymethyl-1,3-dioxolane, 5-ethyl-5-hydroxymethyl-1,3-dioxane and 1,3-dioxolan-4-ylmethanol and 1,3-dioxane-5 -ol (glycerin formulas), as well as amides containing gem-dichlorocyclopropane and 1,3-dioxolane fragments were obtained. The acid chlorides, 1,3-dioxacycloalkanes and secondary amines were prepared according to standard basic methods. Esters and amides were synthesized from these starting compounds in a short time and with a quantitative yield (more than 90%). As a result of the synthesis of a mixture of 1,3-dioxolan-4-ylmethyl phenylacetate and 1,3-dioxan-5-yl phenylacetate, the content of the 5-ring cyclic derivative over the 6-chain structure was predominant, which is obviously associated with greater activity in the esterification reaction of primary alcohol than secondary. The screening results showed that the activity relative to wheat of the 1,3-dioxalane ester of 2,4-dichlorophenoxyacetic acid is superior to the Octagon-Extra standard. With respect to peas, derivatives of 2,4-dichlorophenoxyacetic acid and 2,2-dimethyl-4-hydroxymethyl-1,3-dioxolane are close to the standard for inhibition of shoot mass. The results of N-benzyl-N-[(2,2-dichlorocyclopropyl) methyl] -2-phenoxyacetamide and N-[(2,2-dichlorocyclopropyl) methyl]-N-(1,3-dioxolan-4-ylmethyl)-2-phenoxyacetamide with respect to peas and wheat also showed a marked herbicidal effect, close in value to the reference one. The test results of synthesized benzamides on wheat showed that, at a concentration of 100 mg/l, the compounds act approximately the same as the reference preparation at a dose of 50 mg/l. The obtained results prove the prospects of creating herbicidal preparations based on phenoxy- chlorides and 2,4-dichlorophenoxyacetic acids containing 1,3-dioxacycloalkane fragments. Therefore, these objects are very attractive for further study and synthesis of biologically active compounds containing the above pharmacophore groups.
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7

An, Kyung-Mi, Chang-Hee Hong, Hyun-Jung Kwak, Shuolin Cui, Hyo-Jung Song, Joon-Tae Park, An-Na Moon, et al. "3-Aryl-3-(isoxazol-3-yl)propanoic Acids and 2-Aryloxyacetic Acids as Potent GPR40 Agonists." Bulletin of the Korean Chemical Society 38, no. 8 (August 2017): 838–44. http://dx.doi.org/10.1002/bkcs.11178.

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8

Amoroso, Rosa, Giancarlo Bettoni, Maria Luisa Tricca, Fulvio Loiodice, and Savina Ferorelli. "Direct resolution of α-monoalkyl-α-aryloxyacetic acids via ester or imide derivatives." Il Farmaco 53, no. 1 (January 1998): 73–79. http://dx.doi.org/10.1016/s0014-827x(97)00010-4.

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9

Lyakhov, S. A., E. A. Lyakhova, N. N. Panchenko, L. A. Litvinova, and S. A. Andronati. "ChemInform Abstract: Synthesis and Antiviral Activity of Novel Bis-Acridinylhydrazides of Aryloxyacetic Acids." ChemInform 33, no. 22 (May 21, 2010): no. http://dx.doi.org/10.1002/chin.200222142.

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10

TSUDA, YOSHIKO, KENICHI KAWAI, and SHOICHI NAKAJIMA. "Microbial reduction and resolution of herbicidal 2-alkyl-2-aryloxyacetic acids by Gloeosporium olivarum." CHEMICAL & PHARMACEUTICAL BULLETIN 33, no. 5 (1985): 1955–60. http://dx.doi.org/10.1248/cpb.33.1955.

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11

Leung, Joe C. T., and Glenn M. Sammis. "ChemInform Abstract: Radical Decarboxylative Fluorination of Aryloxyacetic Acids Using N-Fluorobenzenesulfonimide and a Photosensitizer." ChemInform 46, no. 30 (July 2015): no. http://dx.doi.org/10.1002/chin.201530050.

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12

VILLEMIN, D., and M. HAMMADI. "ChemInform Abstract: Environmentally Desirable Synthesis Without Use of Organic Solvent. Synthesis of Aryloxyacetic Acids." ChemInform 28, no. 9 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199709076.

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13

Leuci, Rosalba, Leonardo Brunetti, Antonio Laghezza, Luca Piemontese, Antonio Carrieri, Leonardo Pisani, Paolo Tortorella, Marco Catto, and Fulvio Loiodice. "A New Series of Aryloxyacetic Acids Endowed with Multi-Target Activity towards Peroxisome Proliferator-Activated Receptors (PPARs), Fatty Acid Amide Hydrolase (FAAH), and Acetylcholinesterase (AChE)." Molecules 27, no. 3 (January 31, 2022): 958. http://dx.doi.org/10.3390/molecules27030958.

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A new series of aryloxyacetic acids was prepared and tested as peroxisome proliferator-activated receptors (PPARs) agonists and fatty acid amide hydrolase (FAAH) inhibitors. Some compounds exhibited an interesting dual activity that has been recently proposed as a new potential therapeutic strategy for the treatment of Alzheimer’s disease (AD). AD is a multifactorial pathology, hence multi-target agents are currently one of the main lines of research for the therapy and prevention of this disease. Given that cholinesterases represent one of the most common targets of recent research, we decided to also evaluate the effects of our compounds on the inhibition of these specific enzymes. Interestingly, two of these compounds, (S)-5 and 6, showed moderate activity against acetylcholinesterase (AChE) and even some activity, although at high concentration, against Aβ peptide aggregation, thus demonstrating, in agreement with the preliminary dockings carried out on the different targets, the feasibility of a simultaneous multi-target activity towards PPARs, FAAH, and AChE. As far as we know, these are the first examples of molecules endowed with this pharmacological profile that might represent a promising line of research for the identification of novel candidates for the treatment of AD.
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14

KITAGAWA, Masayuki, Kenjiro YAMAMOTO, Shinichi KATAKURA, Hideyuki KANNO, Koji YAMADA, Takayasu NAGAHARA, and Makoto TANAKA. "Aryloxyacetic Acid Diuretics with Uricosuric Activity. II. Substituted ((4-Oxo-4H-1-benzopyran-7-yl)oxy)acetic Acids and the Related Compounds." CHEMICAL & PHARMACEUTICAL BULLETIN 39, no. 10 (1991): 2681–90. http://dx.doi.org/10.1248/cpb.39.2681.

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15

KITAGAWA, M., K. YAMAMOTO, S. KATAKURA, H. KANNO, K. YAMADA, T. NAGAHARA, and M. TANAKA. "ChemInform Abstract: Aryloxyacetic Acid Diuretics with Uricosuric Activity. Part 2. Substituted ((4-Oxo-4H-1-benzopyran-7-yl)oxy)acetic Acids and the Related Compounds." ChemInform 23, no. 19 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199219193.

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16

Temporini, Caterina, Enrica Calleri, Giuseppe Fracchiolla, Giuseppe Carbonara, Fulvio Loiodice, Antonio Lavecchia, Paolo Tortorella, Gloria Brusotti, and Gabriella Massolini. "Enantiomeric separation of 2-aryloxyalkyl- and 2-arylalkyl-2-aryloxyacetic acids on a Penicillin G Acylase-based chiral stationary phase: Influence of the chemical structure on retention and enantioselectivity." Journal of Pharmaceutical and Biomedical Analysis 45, no. 2 (October 2007): 211–18. http://dx.doi.org/10.1016/j.jpba.2007.06.005.

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17

Abdel Hamid, Hamida M., El Sayed Ramadan, Mohamed Hagar, and El Sayed H. El Ashry. "Synthesis of Aryloxyacetic Acids, Esters, and Hydrazides Assisted by Microwave Irradiation." ChemInform 35, no. 29 (July 20, 2004). http://dx.doi.org/10.1002/chin.200429083.

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18

VORONKOV, M. G., G. DOLMAA, N. I. GOLOVANOVA, A. I. ALBANOV, and E. I. DUBINSKAYA. "ChemInform Abstract: Synthetic Phytohormones. Part 11. Triorganylsilylmethyl Esters of Aryloxyacetic Acids." Chemischer Informationsdienst 17, no. 45 (November 11, 1986). http://dx.doi.org/10.1002/chin.198645256.

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19

HARTMANN, W., W. STEINKE, J. GLOEDE, and H. GROSS. "ChemInform Abstract: α-Substituted Phosphonates. Part 48. Synthesis of α-Phosphorylated Aryloxyacetic Acids." Chemischer Informationsdienst 17, no. 35 (September 2, 1986). http://dx.doi.org/10.1002/chin.198635259.

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20

TSUDA, Y., K. KAWAI, and S. NAKAJIMA. "ChemInform Abstract: MICROBIAL REDUCTION AND RESOLUTION OF HERBICIDAL 2-ALKYL-2-ARYLOXYACETIC ACIDS BY GLOEOSPORIUM OLIVARUM." Chemischer Informationsdienst 16, no. 45 (November 12, 1985). http://dx.doi.org/10.1002/chin.198545323.

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