Bibliografías temáticas / Aryloxyacetic acids

Literatura académica sobre el tema "Aryloxyacetic acids"

Autor: Grafiati
Publicado: 18 de mayo de 2024

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Artículos de revistas sobre el tema "Aryloxyacetic acids"

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Berger, Michael, John D. Herszman, Yuji Kurimoto, Goswinus H. M. de Kruijff, Aaron Schüll, Sven Ruf y Siegfried R. Waldvogel. "Metal-free electrochemical fluorodecarboxylation of aryloxyacetic acids to fluoromethyl aryl ethers". Chemical Science 11, n.º 23 (2020): 6053–57. http://dx.doi.org/10.1039/d0sc02417a.

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Li, Zheng, Jin-Lan Yu, Jing-Ya Yang, Sheng-Yi Shi y Xi-Cun Wang. "Polymer-supported Dichlorophosphate: A Recoverable New Reagent for Synthesis of 2-amino-1,3,4-thiadiazoles". Journal of Chemical Research 2005, n.º 5 (mayo de 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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Abdel Hamid, Hamida M., El Sayed Ramadan, Mohamed Hagar y El Sayed H. El Ashry. "Synthesis of Aryloxyacetic Acids, Esters, and Hydrazides Assisted by Microwave Irradiation". Synthetic Communications 34, n.º 3 (31 de diciembre de 2004): 377–82. http://dx.doi.org/10.1081/scc-120027275.

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Leung, Joe C. T. y Glenn M. Sammis. "Radical Decarboxylative Fluorination of Aryloxyacetic Acids UsingN-Fluorobenzenesulfonimide and a Photosensitizer". European Journal of Organic Chemistry 2015, n.º 10 (5 de febrero de 2015): 2197–204. http://dx.doi.org/10.1002/ejoc.201500038.

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Villemin, Didier y Mohamed Hammadi. "Environmentally Desirable Synthesis Without Use of Organic Solvent. Synthesis of Aryloxyacetic Acids". Synthetic Communications 26, n.º 23 (diciembre de 1996): 4337–41. http://dx.doi.org/10.1080/00397919608003836.

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Raskil’dina, Gul’nara Z., Evgeniya A. Yakovenko, Luisa M. M. Mryasova y 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, n.º 1 (30 de diciembre de 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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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, n.º 8 (agosto de 2017): 838–44. http://dx.doi.org/10.1002/bkcs.11178.

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Amoroso, Rosa, Giancarlo Bettoni, Maria Luisa Tricca, Fulvio Loiodice y Savina Ferorelli. "Direct resolution of α-monoalkyl-α-aryloxyacetic acids via ester or imide derivatives". Il Farmaco 53, n.º 1 (enero de 1998): 73–79. http://dx.doi.org/10.1016/s0014-827x(97)00010-4.

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

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TSUDA, YOSHIKO, KENICHI KAWAI y SHOICHI NAKAJIMA. "Microbial reduction and resolution of herbicidal 2-alkyl-2-aryloxyacetic acids by Gloeosporium olivarum." CHEMICAL & PHARMACEUTICAL BULLETIN 33, n.º 5 (1985): 1955–60. http://dx.doi.org/10.1248/cpb.33.1955.

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Tesis sobre el tema "Aryloxyacetic acids"

1

Kumar, Amal K. "Aryloxyacetic acids : potential ligands for monomeric organotin carboxylates : on the preparation, structure and biological properties of organotin (IV) aryloxyacetates". Thesis, University of North Bengal, 1986. http://hdl.handle.net/123456789/754.

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Capítulos de libros sobre el tema "Aryloxyacetic acids"

1

Martin, Robert. "Compounds Derived from Aryloxyacetic Acids". En Aromatic Hydroxyketones: Preparation and Physical Properties, 1353–68. Dordrecht: Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-1-4020-9787-4_14.

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Martin, Robert. "Compounds derived from aryloxyacetic acids". En Handbook of Hydroxyacetophenones: Preparation and Physical Properties, 703–18. Dordrecht: Springer Netherlands, 2005. http://dx.doi.org/10.1007/1-4020-2291-3_5.

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Martin, Robert. "Compounds derived from acyloxy-and aryloxyacetic acids". En Handbook of Hydroxyacetophenones: Preparation and Physical Properties, 731–41. Dordrecht: Springer Netherlands, 2005. http://dx.doi.org/10.1007/1-4020-2291-3_7.

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