Synthesis of 9-alkyl-6-amino[1,2,4]triazolo[3,4-c]-5-azaquinoxalines. Mild and effective SNAr amination of highly electron-poor heterocycles
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. The Combinatorial Synthesis of Bicyclic Privileged Structures or Privileged Substructures
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5. [1,2,4]Triazolo[4,3-a]quinoxalin-4-amines: a new class of A1 receptor selective adenosine antagonists
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1. Bicyclic 5-6 Systems With One Bridgehead (Ring Junction) Nitrogen Atom: Three Extra Heteroatoms 2:1;Comprehensive Heterocyclic Chemistry IV;2022
2. Amide-controlled, one-pot synthesis of tri-substituted purines generates structural diversity and analogues with trypanocidal activity;Scientific Reports;2015-03-16
3. Microwave-promoted piperidination of halopyridines: a comparison between Ullmann, Buchwald-Hartwig and uncatalysed SN Ar reactions;Applied Organometallic Chemistry;2012-05-09
4. Five-Membered Ring Systems: With More than One N Atom;Progress in Heterocyclic Chemistry;2011
5. ChemInform Abstract: Synthesis of 9-Alkyl-6-amino[1,2,4]triazolo[3,4-c]-5-azaquinoxalines. Mild and Effective SNAr Amination of Highly Electron-Poor Heterocycles.;ChemInform;2010-07-24
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