Thematische Bibliographien / Aryloxyacetic acids / Zeitschriftenartikel
Um die anderen Arten von Veröffentlichungen zu diesem Thema anzuzeigen, folgen Sie diesem Link: Aryloxyacetic acids.

Zeitschriftenartikel zum Thema „Aryloxyacetic acids“

Autor: Grafiati
Veröffentlicht am 18. Mai 2024

Geben Sie eine Quelle nach APA, MLA, Chicago, Harvard und anderen Zitierweisen an

Wählen Sie eine Art der Quelle aus:

Machen Sie sich mit Top-20 Zeitschriftenartikel für die Forschung zum Thema "Aryloxyacetic acids" bekannt.

Neben jedem Werk im Literaturverzeichnis ist die Option "Zur Bibliographie hinzufügen" verfügbar. Nutzen Sie sie, wird Ihre bibliographische Angabe des gewählten Werkes nach der nötigen Zitierweise (APA, MLA, Harvard, Chicago, Vancouver usw.) automatisch gestaltet.

Sie können auch den vollen Text der wissenschaftlichen Publikation im PDF-Format herunterladen und eine Online-Annotation der Arbeit lesen, wenn die relevanten Parameter in den Metadaten verfügbar sind.

Sehen Sie die Zeitschriftenartikel für verschiedene Spezialgebieten durch und erstellen Sie Ihre Bibliographie auf korrekte Weise.

1

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

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
2

Li, Zheng, Jin-Lan Yu, Jing-Ya Yang, Sheng-Yi Shi und Xi-Cun Wang. „Polymer-supported Dichlorophosphate: A Recoverable New Reagent for Synthesis of 2-amino-1,3,4-thiadiazoles“. Journal of Chemical Research 2005, Nr. 5 (Mai 2005): 341–43. http://dx.doi.org/10.3184/0308234054323913.

Der volle Inhalt der Quelle
Annotation:
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.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
3

Abdel Hamid, Hamida M., El Sayed Ramadan, Mohamed Hagar und El Sayed H. El Ashry. „Synthesis of Aryloxyacetic Acids, Esters, and Hydrazides Assisted by Microwave Irradiation“. Synthetic Communications 34, Nr. 3 (31.12.2004): 377–82. http://dx.doi.org/10.1081/scc-120027275.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
4

Leung, Joe C. T., und Glenn M. Sammis. „Radical Decarboxylative Fluorination of Aryloxyacetic Acids UsingN-Fluorobenzenesulfonimide and a Photosensitizer“. European Journal of Organic Chemistry 2015, Nr. 10 (05.02.2015): 2197–204. http://dx.doi.org/10.1002/ejoc.201500038.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
5

Villemin, Didier, und Mohamed Hammadi. „Environmentally Desirable Synthesis Without Use of Organic Solvent. Synthesis of Aryloxyacetic Acids“. Synthetic Communications 26, Nr. 23 (Dezember 1996): 4337–41. http://dx.doi.org/10.1080/00397919608003836.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
6

Raskil’dina, Gul’nara Z., Evgeniya A. Yakovenko, Luisa M. M. Mryasova und 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, Nr. 1 (30.12.2018): 91–97. http://dx.doi.org/10.6060/ivkkt.20196201.5753.

Der volle Inhalt der Quelle
Annotation:
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.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
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, Nr. 8 (August 2017): 838–44. http://dx.doi.org/10.1002/bkcs.11178.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
8

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

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
9

Lyakhov, S. A., E. A. Lyakhova, N. N. Panchenko, L. A. Litvinova und S. A. Andronati. „ChemInform Abstract: Synthesis and Antiviral Activity of Novel Bis-Acridinylhydrazides of Aryloxyacetic Acids.“ ChemInform 33, Nr. 22 (21.05.2010): no. http://dx.doi.org/10.1002/chin.200222142.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
10

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

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
11

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

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
12

VILLEMIN, D., und M. HAMMADI. „ChemInform Abstract: Environmentally Desirable Synthesis Without Use of Organic Solvent. Synthesis of Aryloxyacetic Acids.“ ChemInform 28, Nr. 9 (04.08.2010): no. http://dx.doi.org/10.1002/chin.199709076.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
13

Leuci, Rosalba, Leonardo Brunetti, Antonio Laghezza, Luca Piemontese, Antonio Carrieri, Leonardo Pisani, Paolo Tortorella, Marco Catto und 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, Nr. 3 (31.01.2022): 958. http://dx.doi.org/10.3390/molecules27030958.

Der volle Inhalt der Quelle
Annotation:
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.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
14

KITAGAWA, Masayuki, Kenjiro YAMAMOTO, Shinichi KATAKURA, Hideyuki KANNO, Koji YAMADA, Takayasu NAGAHARA und 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, Nr. 10 (1991): 2681–90. http://dx.doi.org/10.1248/cpb.39.2681.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
15

KITAGAWA, M., K. YAMAMOTO, S. KATAKURA, H. KANNO, K. YAMADA, T. NAGAHARA und 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, Nr. 19 (22.08.2010): no. http://dx.doi.org/10.1002/chin.199219193.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
16

Temporini, Caterina, Enrica Calleri, Giuseppe Fracchiolla, Giuseppe Carbonara, Fulvio Loiodice, Antonio Lavecchia, Paolo Tortorella, Gloria Brusotti und 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, Nr. 2 (Oktober 2007): 211–18. http://dx.doi.org/10.1016/j.jpba.2007.06.005.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
17

Abdel Hamid, Hamida M., El Sayed Ramadan, Mohamed Hagar und El Sayed H. El Ashry. „Synthesis of Aryloxyacetic Acids, Esters, and Hydrazides Assisted by Microwave Irradiation.“ ChemInform 35, Nr. 29 (20.07.2004). http://dx.doi.org/10.1002/chin.200429083.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
18

VORONKOV, M. G., G. DOLMAA, N. I. GOLOVANOVA, A. I. ALBANOV und E. I. DUBINSKAYA. „ChemInform Abstract: Synthetic Phytohormones. Part 11. Triorganylsilylmethyl Esters of Aryloxyacetic Acids.“ Chemischer Informationsdienst 17, Nr. 45 (11.11.1986). http://dx.doi.org/10.1002/chin.198645256.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
19

HARTMANN, W., W. STEINKE, J. GLOEDE und H. GROSS. „ChemInform Abstract: α-Substituted Phosphonates. Part 48. Synthesis of α-Phosphorylated Aryloxyacetic Acids.“ Chemischer Informationsdienst 17, Nr. 35 (02.09.1986). http://dx.doi.org/10.1002/chin.198635259.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
20

TSUDA, Y., K. KAWAI und S. NAKAJIMA. „ChemInform Abstract: MICROBIAL REDUCTION AND RESOLUTION OF HERBICIDAL 2-ALKYL-2-ARYLOXYACETIC ACIDS BY GLOEOSPORIUM OLIVARUM“. Chemischer Informationsdienst 16, Nr. 45 (12.11.1985). http://dx.doi.org/10.1002/chin.198545323.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
Wir bieten Rabatte auf alle Premium-Pläne für Autoren, deren Werke in thematische Literatursammlungen aufgenommen wurden. Kontaktieren Sie uns, um einen einzigartigen Promo-Code zu erhalten!

Zur Bibliographie