A Convenient Synthesis of Fluorinated Pyrazolo[3,4-b]pyridine and Pyrazolo[3,4-d]pyrimidine Nucleosides
Synthesis , 2009, 05, 731-740
DOI: 10.1055/s-0028-1083365
Iaroshenko V. O.; Sevenard D. V.; Kotljarov A.; Volochnyuk D. M.; Tolmachev A. O.; Sosnovskikh V. Y.
Starting from 5-amino-1-(2,3-O-isopropylidene-β-d-ribofuranosyl)-1H-pyrazole, fluorine-containing 1,3-CCC-, 1,3-CNC-dielectrophiles and 2,4,6-tris(trifluoromethyl)-1,3,5-triazine, a set of fluorinated pyrazolo[3,4-b]pyridine and pyrazolo[3,4-d]pyrimidine nucleosides was obtained. Synthetic access to stable 4-(polyfluoroalkyl)-4,7-dihydro-1H-pyrazolo[3,4-b]pyridin-4-ole was elaborated, which can be considered to be mimetics of the putative transition state involved in adenosine deaminase activity.
![A Convenient Synthesis of Fluorinated Pyrazolo[3,4-b]pyridine and Pyrazolo[3,4-d]pyrimidine Nucleosides](/images/publications/s-0028-1083365.png)
Iaroshenko V. O.; Sevenard D. V.; Kotljarov A.; Volochnyuk D. M.; Tolmachev A. O.; Sosnovskikh V. Y.
Synthesis 2009, 05, 731-740
DOI: 10.1055/s-0028-1083365