858340-88-2Relevant academic research and scientific papers
Regioselective direct arylation of fused 3-nitropyridines and other nitro-substituted heteroarenes: The multipurpose nature of the nitro group as a directing group
Iaroshenko, Viktor O.,Gevorgyan, Ashot,Mkrtchyan, Satenik,Grigoryan, Tatevik,Movsisyan, Ester,Villinger, Alexander,Langer, Peter
, p. 316 - 324 (2015/03/03)
We report Pd-and Ni-catalysed, guided and regioselective C-H arylations of a series of fused 3-nitropyridines. The method described here is a facile tool for the chemical functionalisation of drug-like fused pyridines. The scope and limitations of the rea
Design, synthesis and transformation of some heteroannulated 3-aminopyridines - Purine isosteres with exocyclic nitrogen atom
Iaroshenko, Viktor O.,Vilches-Herrera, Marcelo,Gevorgyan, Ashot,Mkrtchyan, Satenik,Arakelyan, Knar,Ostrovskyi, Dmytro,Abbasi, Muhammad S.A.,Supe, Linda,Hakobyan, Ani,Villinger, Alexander,Volochnyuk, Dmitriy M.,Tolmachev, Andrei
supporting information, p. 1217 - 1228 (2013/02/23)
The synthesis of 1-deazapurines and isosteres bearing the exocyclic nitrogen atom at position-1 was developed basing on the formal [3+3]-cyclization reaction of nitro-malonaldehyde with the set of electron-excessive aminoheterocycles. Through the function
PYRROLO[2,3-b] PYRIDINE DERIVATIVES ACTIVE AS KINASE INHIBITORS, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITION COMPRISING THEM
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Page/Page column 40, (2008/06/13)
Compounds which are pyrrolo[2,3-b]pyridine derivatives or pharmaceutically acceptable salts thereof, their preparation process and pharmaceutical compositions comprising them are disclosed; these compounds are useful in the treatment of diseases caused by
