Academic literature on the topic 'Bi-amidine'

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Journal articles on the topic "Bi-amidine"

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Eicher, Theophil, and Ralph Rohde. "Zur Reaktion von Cyclopropenonen mit Azomethinen; VII. Diphenylcyclopropenon und cyclische Amidine: Synthese von bi- und tricyclischen Pyrrolinon-Derivaten." Synthesis 1985, no. 6/7 (1985): 619–25. http://dx.doi.org/10.1055/s-1985-34144.

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Dobashi, Yasuo, Kiyotaka Kobayashi, Norihisa Sato, and Akira Dobashi. "Chiral recognition of 1,1′-bi-2-naphthol enantiomers by twisted amidine derivatives: Rational design of a highly enantioselective receptor." Tetrahedron Letters 39, no. 19 (May 1998): 2985–88. http://dx.doi.org/10.1016/s0040-4039(98)00436-5.

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DOBASHI, Y., K. KOBAYASHI, N. SATO, and A. DOBASHI. "ChemInform Abstract: Chiral Recognition of 1,1′-Bi-2-naphthol Enantiomers by Twisted Amidine Derivatives: Rational Design of a Highly Enantioselective Receptor." ChemInform 29, no. 30 (June 20, 2010): no. http://dx.doi.org/10.1002/chin.199830042.

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4

EICHER, T., and R. ROHDE. "ChemInform Abstract: Zur Reaktion von Cyclopropenonen mit Azomethinen. 7. Mitt. Diphenylcyclopropenon und cyclische Amidine: Synthese von bi- und tricyclischen Pyrrolinon-Derivaten." Chemischer Informationsdienst 16, no. 47 (November 26, 1985). http://dx.doi.org/10.1002/chin.198547084.

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Dissertations / Theses on the topic "Bi-amidine"

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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, aminooxadiazolones et iminooxadiazolidinones. Les activités antipaludiques in vitro et in vivo des composés obtenus ont été évaluées
Amidoxime and oxadiazolone prodrug strategies have been applied to new N-monosubstituted bis-alkylamidine drugs which were synthesised by a new divergent strategy based on the use of the N-substitued bis-alkyloxadiazolone as an intermediate. Bis-alkylamidoxime N-alkylsulfonyles derivatives have been developed to obtain in vitro stable structures preserving potent oral activities. Finally, new bis-alkylguanidine drugs were synthesised as well as their bioprecursors N-hydroxyguanidines, aminooxadiazolones and iminooxadiazolidinones. In vitro and in vivo antiplasmodial activities of the obtained compounds were evaluated
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