Academic literature on the topic 'Alkylguanidines'

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Journal articles on the topic "Alkylguanidines"

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Schuchardt, Ulf, Rogério Matheus Vargas, and Georges Gelbard. "Alkylguanidines as catalysts for the transesterification of rapeseed oil." Journal of Molecular Catalysis A: Chemical 99, no. 2 (1995): 65–70. http://dx.doi.org/10.1016/1381-1169(95)00039-9.

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Deli, József, Tamás Lóránd, Dezsö Szabó, András Földesi, and Adolf Zschunke. "Synthesis of 2-amino-8-benzylidene-4-phenyl-3,4,5,6,7,8-hexahydro- and -5,6,7,8-tetrahydroquinazoline derivatives." Collection of Czechoslovak Chemical Communications 50, no. 7 (1985): 1602–10. http://dx.doi.org/10.1135/cccc19851602.

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Base-catalyzed reaction of 2,6-dibenzylidenecyclohexanone and alkylguanidines gave 2-alkylamino-8-benzylidene-4-phenyl-3,4,5,6,7,8-hexahydroquinazolines IVa-c, which were oxidized to 2-alkylamino-8-benzylidene-4-phenyl-5,6,7,8-tetrahydroquinazolines Va-c. The acylamino (VIa-c, VIIa-d, IXa,b) and diacylamino derivatives (VIIIa,b) of the 2-amino-8-benzylidene-4-pheny]-3,4,5,6,7,8-hexahydroquinazoline (II), 2-amino-8-benzylidene-4-phenyl-5,6,7,8-tetrahydroquinazoline (III) and compounds Va-c have also been prepared. These compounds having the E-configuration were converted into the Z isomers XIIa
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Hayessen, R., V. M. Mirsky, and K. D. Heckmann. "Anion-sensitive properties of alkylguanidines in membrane electrodes and monomolecular layers." Sensors and Actuators B: Chemical 32, no. 3 (1996): 215–20. http://dx.doi.org/10.1016/s0925-4005(97)80032-9.

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Farley, Jerry M., Stephen M. Vogel, and Toshio Narahashi. "Block of single acetylcholine-activated channels in chick myotubes by alkylguanidines." Pfl�gers Archiv European Journal of Physiology 406, no. 6 (1986): 629–35. http://dx.doi.org/10.1007/bf00584031.

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Schuchardt, Ulf, Rogério Matheus Vargas, and Georges Gelbard. "Transesterification of soybean oil catalyzed by alkylguanidines heterogenized on different substituted polystyrenes." Journal of Molecular Catalysis A: Chemical 109, no. 1 (1996): 37–44. http://dx.doi.org/10.1016/1381-1169(96)00014-3.

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Zeghida, Walid, Julien Debray, Carine Michel, Anne Milet, Pascal Dumy, and Martine Demeunynck. "Synthesis of N-acridinyl-N′-alkylguanidines: Dramatic influence of amine to guanidine replacement on the physicochemical properties." Bioorganic & Medicinal Chemistry Letters 18, no. 17 (2008): 4779–82. http://dx.doi.org/10.1016/j.bmcl.2008.07.100.

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Tin, Ma K. T., Natesan Thirupathi, Glenn P. A. Yap, and Darrin S. Richeson. "Guanidinate anions and dianions. Reactions involving alkylguanidines, (RNH)2CNR (R = i-Pr or Cy), and metal amido complexes M(NMe2)5 (M = Ta or Nb)." Journal of the Chemical Society, Dalton Transactions, no. 17 (1999): 2947–51. http://dx.doi.org/10.1039/a904072b.

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GUAN, Feng, Hong ZHONG, Guang-yi LIU, Sheng-gui ZHAO, and Liu-yin XIA. "Flotation of aluminosilicate minerals using alkylguanidine collectors." Transactions of Nonferrous Metals Society of China 19, no. 1 (2009): 228–34. http://dx.doi.org/10.1016/s1003-6326(08)60257-5.

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Sercheli, Ricardo, Rogério Matheus Vargas, and Ulf Schuchardt. "Alkylguanidine-catalyzed heterogeneous transesterification of soybean oil." Journal of the American Oil Chemists' Society 76, no. 10 (1999): 1207–10. http://dx.doi.org/10.1007/s11746-999-0095-2.

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Degardin, Mélissa, Sharon Wein, Jean-Frédéric Duckert, et al. "Development of the First Oral Bioprecursors of Bis-alkylguanidine Antimalarial Drugs." ChemMedChem 9, no. 2 (2014): 300–304. http://dx.doi.org/10.1002/cmdc.201300419.

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Dissertations / Theses on the topic "Alkylguanidines"

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Degardin, Mélissa. "Synthèse et activités antipaludiques de bis-alkylamidines N-monosubstituées, bis-alkylguanidines et de leurs bioprécurseurs de type amidoxime et O-dérivés." Montpellier 2, 2009. http://www.theses.fr/2009MON20165.

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Des stratégies prodrogues amidoxime et oxadiazolone ont été appliquées à de nouvelles drogues bis-alkylamidines N-monosubstituées que nous avons synthétisées selon une nouvelle stratégie divergente basée sur l'utilisation de la bis-alkyloxadiazolone N-substituée comme intermédiaire de synthèse. Des dérivés N-alkylsulfonyles de bis-alkylamidoximes ont été développés dans le but d'obtenir des structures stables in vitro tout en conservant de fortes activités orales. Enfin, de nouvelles drogues bis-alkylguanidines ont été synthétisées ainsi que leurs bioprécurseurs N-hydroxyguanidines, aminooxadi
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I, D'Agostino. "Polyalkylguanidines: new weapons to tackle bacterial resistance." Doctoral thesis, Università di Siena, 2019. http://hdl.handle.net/11365/1070884.

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In this historical period known as the antibiotic crisis era, the ever faster rise of bacterial strains resistant to the clinically used antibiotics along with the scientific research silent gap in the antibacterial field is treating seriously to the worldwide public health. Hence, we urgently need to develop new antibacterials agents with an innovative mode of action, able to trick the mechanisms of the pathogen resistance. In this alarming frame, aware of the antibacterial properties of guanidine moieties, Prof. M. Botta and his research group have evaluated the biological activity of a lin
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Ardino, Claudia. "Divergent synthesis and MoA investigation of antibacterial alkylguanidino ureas." Doctoral thesis, Università di Siena, 2022. http://hdl.handle.net/11365/1203167.

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The ever-faster rise of antimicrobial resistance (AMR) represents still nowadays a major Public Health issue to concern. Hence, new chemical entities with innovative Modes of Action (MoAs) are required. In this work is reported the extension of an already existing library of AlkylGuanidino Ureas (AGUs), endowed with broad-spectrum bactericidal activity, and a deeper insight is given concerning their mechanisms of action towards bacterial membranes. In fact, most promising derivatives of the series were submitted to model or simulated membrane-based investigations by means of LUVs interaction e
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Conference papers on the topic "Alkylguanidines"

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D’Agostino, Ilaria, Jean-Denis Docquier, and Maurizio Botta. "AlkylGuanidino Ureas, from a Serendipitous Discovery to a Rational Design: Innovative Membrane-Active Antibacterial Agents." In The 2nd International Electronic Conference on Antibiotics—Drugs for Superbugs: Antibiotic Discovery, Modes of Action and Mechanisms of Resistance. MDPI, 2022. http://dx.doi.org/10.3390/eca2022-12756.

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