Relevant bibliographies by topics / Phenylcarbamates

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Reports

Academic literature on the topic 'Phenylcarbamates'

Author: Grafiati
Published: 7 June 2025
Last updated: 2 August 2025

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Journal articles on the topic "Phenylcarbamates"

1

Rosevear, J., and JFK Wilshire. "A Comparison of the Reactions of Some Ethyl N-Arylcarbamates With Those of the Corresponding Acetanilides. II. Amidomethylation With N-Hydroxy-methylphthalimide." Australian Journal of Chemistry 43, no. 2 (1990): 339. http://dx.doi.org/10.1071/ch9900339.

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The reactions of some ethyl N- arylcarbamates and of the corresponding acetanilides towards 1 equiv. of N-hydroxymethylphthalimide in concentrated sulfuric acid at 50° have been compared with one another. In the case of certain para-substituted compounds, amidomethylation occurs more readily ortho to the carbamate group than to the N-acetyl group. The diagnostic use of (D6)benzene as a 1H n.m.r. solvent, particularly for the structural elucidation of the ortho-( phthalimidomethyl )- phenylcarbamates and -acetanilides, is reported. Acidic treatment of the ortho -( phthalimidomethyl ) phenylcarb
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Mona, Sobhi, Patrick Ravanel, Xavier de Chérade, Michel Bergon, Jean-Pierre Calmon, and Michel Tissut. "Uncoupling activity of some N-phenylcarbamates." Pesticide Biochemistry and Physiology 27, no. 3 (1987): 261–66. http://dx.doi.org/10.1016/0048-3575(87)90055-1.

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Daub, Jörg, Lothar Jakob, Josef Salbeck, and Yoshio Okamoto. "Modellverbindungen für Elektronentransfer in räumlich geordneten Systemen: Chirale und achirale Triptycenazulenchinone." CHIMIA 39, no. 12 (1985): 393. https://doi.org/10.2533/chimia.1985.393.

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Stable bitriptyceneazulene quinones have been prepared by Lewis acid induced coupling of triptyceneazulene quinones. Resolution of the enantiomers succeeded by high performance liquid chromatography (HPLC) on phenylcarbamates of cellulose. Some chiroptical properties of the enantiomers are reported. Electron transfer properties have been investigated by cyclovoltammetry.
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Hollomon, Derek W., Jenny A. Butters, Helen Barker та Len Hall. "Fungal β-Tubulin, Expressed as a Fusion Protein, Binds Benzimidazole and Phenylcarbamate Fungicides". Antimicrobial Agents and Chemotherapy 42, № 9 (1998): 2171–73. http://dx.doi.org/10.1128/aac.42.9.2171.

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ABSTRACT Benzimidazoles are important antitubulin agents used in veterinary medicine and plant disease control. Resistance is a practical problem correlated with single amino acid changes in β-tubulin and is often linked to greater sensitivity to phenylcarbamates. This negative cross-resistance creates opportunities for durable antiresistance strategies. Attempts to understand the molecular basis of benzimidazole resistance have been hampered by the inability to purify tubulin from filamentous fungi. We have overcome some of these problems by expressing β-tubulin as a fusion with a maltose bin
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Hajinasiri, Rahimeh, and Halimeh Khatoon Khajavi. "Reaction of N-Methylimidazole and Dimethyl Acetylenedicarboxylate in the Presence of N-Phenyl Carbamate under Solvent-free Conditions." Zeitschrift für Naturforschung B 69, no. 4 (2014): 439–43. http://dx.doi.org/10.5560/znb.2014-3318.

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An efficient synthesis of 1,2,3-functionalized imidazoles and dimethyl-2-[(alkoxycarbonyl)- anilino]-2-butenedioate derivatives via one-pot reactions between N-methylimidazole, dimethyl acetylenedicarboxylate and N-phenylcarbamates under solvent-free conditions is described. The mild reaction conditions and good yields exhibit the synthetic advantage of this method.
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Takahashi, Junya, Osamu Kirino, Chiyozo Takayama, and Katsuzo Kamoshita. "Studies on fungicidal activity of N-phenylcarbamates." Journal of Chromatography A 436 (January 1988): 316–22. http://dx.doi.org/10.1016/s0021-9673(00)94589-8.

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Haufe, Günter, Dörthe Wölker, and Roland Fröhlich. "Selectivity of Biohydroxylation withBeauveriabassianaoftrans-2-FluorocycloalkylN-Phenylcarbamates." Journal of Organic Chemistry 67, no. 9 (2002): 3022–28. http://dx.doi.org/10.1021/jo016332j.

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VELIKORODOV, A. V., T. N. MAKSIMOVA, and V. B. MOCHALIN. "ChemInform Abstract: Nitration of Alkyl N-Phenylcarbamates." ChemInform 24, no. 36 (2010): no. http://dx.doi.org/10.1002/chin.199336105.

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OHGA, Kazuya, Hiroki OYAMA, and Yoshitaka MUTA. "Chromatographic Optical Resolution on Phenylcarbamates of N-Arylidenechitosans." Analytical Sciences 7, no. 4 (1991): 653–56. http://dx.doi.org/10.2116/analsci.7.653.

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NAGAO, Yukinori, Yoshimoto ABE, Takahisa MISONO, et al. "Synthesis and Biological Activities of Phenylcarbamates and Phenylthiocarbamates." NIPPON KAGAKU KAISHI, no. 6 (1993): 719–27. http://dx.doi.org/10.1246/nikkashi.1993.719.

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Dissertations / Theses on the topic "Phenylcarbamates"

1

Mona, Sobhi. "Mode d'action cellulaire de séries de phenylcarbamates herbicides." Grenoble 1, 1987. http://www.theses.fr/1987GRE10105.

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Un groupe de 45 derives appartenant a la famille des carbamates a ete etudie, pour ses effets herbicides. Ce groupe contient des n-phenylcarbamates d'isopropyle, d'ethyle substitue, de phenyle et des biscarbamates. Dans une premiere partie ont ete analyses les effets de tous ces composes sur le transfert electronique associe a l'activite photosynthetique. . .
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Marty, Jean-Louis. "Métabolisation des phenylcarbamates herbicides : rôle des enzymes et des microorganismes." Perpignan, 1987. http://www.theses.fr/1987PERP0039.

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Truchan, Nadine [Verfasser]. "Palladium-katalysierte oxidative Kupplung von Phenolen mit Phenylcarbamaten und Studien zur Synthese von (+)-Tetrandrin / Nadine Truchan." München : Verlag Dr. Hut, 2019. http://d-nb.info/1188516035/34.

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Andrä, Matthias. "Synthese und In-vitro-Pharmakologie neuer Phenylcarbamate als Liganden für nicotinische Acetylcholin-Rezeptoren (nAChR) /." 2005. http://www.gbv.de/dms/bs/toc/509423310.pdf.

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Andrä, Matthias [Verfasser]. "Synthese und In-vitro-Pharmakologie neuer Phenylcarbamate als Liganden für nicotinische Acetylcholin-Rezeptoren (nAChR) / vorgelegt von Matthias Andrä." 2005. http://d-nb.info/977846679/34.

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Book chapters on the topic "Phenylcarbamates"

1

Fujimura, Makoto, Kenji Oeda, Hirokazu Inoue, and Toshiro Kato. "Mechanism of Action ofN-Phenylcarbamates in Benzimidazole-ResistantNeurosporaStrains." In ACS Symposium Series. American Chemical Society, 1990. http://dx.doi.org/10.1021/bk-1990-0421.ch015.

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Wohlfarth, Ch. "Second virial coefficient of poly(vinyl phenylcarbamate)." In Polymer Solutions. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-02890-8_747.

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Mukaiyama, Teruaki. "Ring-opening polymerization." In Challenges in Synthetic Organic Chemistry. Oxford University PressOxford, 1990. http://dx.doi.org/10.1093/oso/9780198556442.003.0005.

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Abstract In Chapter 3, I have described the chemistry in which compounds with cumulated double bonds (X=Y=Z) or an unsaturated carbon-carbon bond (e.g. isocyanate, carbodiimide, alkoxyacetylene, vinyl ether, and ketene acetal) undergo reaction with aldoximes, primary nitroalkanes, hydroxamic acids, etc. to give intramolecular dehydration products (e.g. nitriles, nitrile oxides, isocyanates, etc.) in high yields. In order to broaden the scope of such dehydration reactions, we examined the dehydration of aldoximes with diethyl N-phenyliminocarbonate, which can be regarded as the acetal of isocya
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Reports on the topic "Phenylcarbamates"

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I. A. Parshikov, Igor A. OXIDATION OF GERANYL-N-PHENYLCARBAMATE BY FUNGUS BEAUVERIA BASSIANA WITH AIM TO OBTANING OF NEW ANTI-CANCER DRUGS. Intellectual Archive, 2020. http://dx.doi.org/10.32370/iaj.2427.

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The microbial oxidation of geranyl-N-phenylcarbamate by fungus Beauveria bassiana was investigated. Oxidation of the C3 – C4 double bond of the parent molecule leads to regioselective formation of O-3,4-epoxyheranyl-N-phenylcarbamate in 30 % yield
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Parshikov, Igor. MICROBIAL SYNTHESIS OF POTENTIALLY ANTI-CANCER O-3,4-EPOXYHERANYL-N-PHENYLCARBAMATE. Intellectual Archive, 2020. http://dx.doi.org/10.32370/iaj.2354.

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Journal articles
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