Synthesis of hetarylsubstituted pyrazolo[3,4-c] isoquinolines under Pictet—Spengler reaction conditions

Author:

Bogdan N.M., ,Borodkin Ya.S.,Sujkov S.Yu.,Khairulin A.R.,Bogza S.L., , , ,

Publisher

National Academy of Sciences of Ukraine (Co. LTD Ukrinformnauka)

Reference11 articles.

1. 1. Hennig, L., AlvaAstudillo, M., Meusinger, R. & Mann, G. (1993). Synthesis of pyrazolo[3,4-c]isoquinoline and pyrazolo[3,4-b]pyridine derivatives from azomethines and CH-acidic compounds. Monatsh. Chem., 124, No. 89, pp. 893-898. doi: https://doi.org/10.1007/BF00816412

2. 2. Bogza, S. L., Malienko, A. A., Sujkov, S. Yu., Perepichka, I. F., Bogdan, N. M., Dulenko, V. I., Kobrakov, K. I. & Bryce, M. R. (2001). Convenient one pot synthesis of 5-unsubstituted pyrazolo [3,4-c]isoquinolines. J. Heterocyclic Chem., 38, No. 3, pp. 523-525. doi: https://doi.org/10.1002/jhet.5570380238

3. 3. Bogza, S. L., Nikolyukin, Yu. A. & Dulenko V. I. (1994). Intramolecular cyclization of N-(4-aryl-5-pyrazolyl-formamidines. Chem. Heterocycl. Comp., 30, No. 9, pp. 11-20. doi: https://doi.org/10.1007/BF01171178

4. 4. Bogza, S. L., Ivanov, A. V. & Dulenko V. I. (1997). Cyclodesamination of N-azolylformamidines. Synthesis of polyazaheterocycles with isoquinoline and indolo[2,3-c]-pyridine structural fragments. Chem. Heterocycl. Comp., 33, No. 1, pp. 69-73. doi: https://doi.org/10.1007/BF02290749

5. 5. Kobrakov, K. I., Malienko, A. A., Perepichka, I. F., Sujkov, S. Yu., Bryce, M. R., Lyubchik, S. B., Batsanov, A. S., Bogdan, N. M. & Bogza, S. L. (2005). A versatile synthesis of pyrazolo[3,4-c]isoquinoline derivatives by reaction of 4-aryl-5-aminopyrazoles with aryl/heteroaryl aldehydes: the effect of heterocycle on the reaction pathways. Org. Biomol. Chem., 3, No. 5, pp. 932-940. doi: https://doi.org/10.1039/B417002D

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