Academic literature on the topic '5-c]isoquinolines'

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Journal articles on the topic "5-c]isoquinolines"

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Deprets, Stephanie, and Gilbert Kirsch. "ChemInform Abstract: Synthesis of 5-Methylbenzo[b]thieno[2,3-c]isoquinolines and 5-Methylbenzo[b]seleno[2,3-c]isoquinolines." ChemInform 31, no. 25 (2010): no. http://dx.doi.org/10.1002/chin.200025155.

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Deprets, Stéphanie, and Gilbert Kirsch. "Synthesis of 5-Methylbenzo[b]thieno[2,3-c]isoquinolines and5-Methylbenzo[b]seleno[2,3-c]isoquinolines." European Journal of Organic Chemistry 2000, no. 7 (2000): 1353–57. http://dx.doi.org/10.1002/1099-0690(200004)2000:7<1353::aid-ejoc1353>3.0.co;2-a.

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Yugandar, Somaraju, and Hiroyuki Nakamura. "Rhodium(iii)-catalysed carboxylate-directed C–H functionalizations of isoxazoles with alkynes." Chemical Communications 55, no. 58 (2019): 8382–85. http://dx.doi.org/10.1039/c9cc03283e.

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Isoxazolyl-4-carboxylic acids underwent rhodium(iii)-catalysed carboxylate-directed C–H functionalizations with internal alkynes to produce pyranoisoxazolones, isoquinolines, and 5-alkenylisoxazoles controlled by oxidants.
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Bogza, Sergei L., Anna A. Malienko, Sergei Y. U. Sujkov, et al. "Convenient one pot synthesis of 5-unsubstituted pyrazolo [3,4-c]isoquinolines." Journal of Heterocyclic Chemistry 38, no. 2 (2001): 523–25. http://dx.doi.org/10.1002/jhet.5570380238.

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5

Zhang, Bo, and Armido Studer. "1-Trifluoromethylated isoquinolines via radical trifluoromethylation of isonitriles." Org. Biomol. Chem. 12, no. 48 (2014): 9895–98. http://dx.doi.org/10.1039/c4ob02145b.

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A simple and efficient approach to biologically important 1-trifluoroalkylated isoquinolines starting with readily prepared β-aryl-α-isocyano-acrylates and R<sub>f</sub>-I(iii)-reagents (R<sub>f</sub> = CF<sub>3</sub>, C<sub>2</sub>F<sub>5</sub>, C<sub>3</sub>F<sub>7</sub>) is described.
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Hejsek, Miloslav, Jan Slouka, Vojtěch Bekárek, and Antonín Lyčka. "Cyclization Reactions of 2-(6-Azauracil-5-yl)benzoic Acid and Some Its Derivatives." Collection of Czechoslovak Chemical Communications 57, no. 1 (1992): 123–33. http://dx.doi.org/10.1135/cccc19920123.

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2-(6-Azauracil-5-yl)benzoic acid (Ib) and its thio analogue Ia give new heterocyclic compounds, 1,2-dihydro-1,2,4-triazino[5,6-c]isocoumarin-3-one (IVb) and analogous 3-thione IVa, respectively, on treatment with N,N'-dicyclohexylcarbodiimide. A series of substituted 1,2,4-triazino[5,6-c]isoquinolines V-XVI have been prepared from these compounds and from other functional derivatives (II, III) of the acids I.
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Bogza, Sergei L., Konstantin I. Kobrakov, Anna A. Malienko, et al. "ChemInform Abstract: Convenient One Pot Synthesis of 5-Unsubstituted Pyrazolo[3,4-c]isoquinolines." ChemInform 32, no. 35 (2010): no. http://dx.doi.org/10.1002/chin.200135148.

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Kalugin, V. E., and A. M. Shestopalov. "Synthesis of substituted 5-aminobenzothieno[3,2-c]isoquinolines and their sulfinyl and sulfonyl derivatives." Russian Chemical Bulletin 64, no. 4 (2015): 878–82. http://dx.doi.org/10.1007/s11172-015-0948-9.

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Lantos, Ivan, and Haralambos E. Katerinopoulos. "Synthetic transformations of cyclopropyl annulated dihydroisoquinolines." Canadian Journal of Chemistry 69, no. 6 (1991): 1033–37. http://dx.doi.org/10.1139/v91-152.

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Isomeric 3-cyano-3-methyl-2-acetyl-cycloprop[c]isoquinolines, 5 and 6, were prepared by alkylation and cyclopropanation of Reissert compounds and their reactions under basic conditions were examined. Both compounds, under the influence of methoxide, yielded isoquinoline derived products resulting from cleavage of the peripheral C—C bond. The results are postulated to derive from attack of the methoxide on the acyl carbonyl, forming a tetrahedral adduct that undergoes ring opening. Key words: cyclopropanation, ring opening, tetrahedral complex, pyramidalization.
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Chen, Lu, Xian Zhang, Bin Chen, Bin Li, and Yibiao Li. "Synthesis of benzo[4, 5]imidazo[2,1-a]isoquinolines via intramolecular C–H bond functionalization." Chemistry of Heterocyclic Compounds 53, no. 5 (2017): 618–21. http://dx.doi.org/10.1007/s10593-017-2101-1.

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Dissertations / Theses on the topic "5-c]isoquinolines"

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Tber, Zahira. "L'imidazo[1,2-a]pyridine : fonctionnalisation et synthèse des nouveaux polyhétérocycles." Thesis, Orléans, 2016. http://www.theses.fr/2016ORLE2021.

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Les préparations de composés comportant un noyau imidazo[1,2-a]pyridinique constituent un thème de recherche important en synthèse organique, compte tenu des nombreuses activités biologiques qu’ils peuvent présenter. Dans la première partie, nous nous sommes concentrés sur le développement de nouvelles stratégies rapides et efficaces basées sur l’utilisation de cuivre et de fer pour fonctionnaliser la position 6 du cycle imidazo[1,2-a]pyridine avec diverses amines et divers thiols. Ensuite, nous avons appliqué avec succès cette procédure pour la préparation de thioéthers symétriques et dissymé
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