199684-20-3Relevant academic research and scientific papers
Pyrrolo[2,3-d][1,2,3]triazoles as potential antineoplastic agents
Passannanti, Alessandra,Diana, Patrizia,Barraja, Paola,Mingoia, Francesco,Lauria, Antonino,Cirrincione, Girolamo
, p. 1229 - 1235 (2007/10/03)
Halonitropyrrole (1a) underwent nucleophilic substitution by substituted benzylamines (7) to give the intermediates (8), which by reduction and diazotization followed by an intramolecular coupling reaction led to derivatives of the title ring system (10).
Nucleophilic reactions in the pyrrole series: Displacement of halogen as a tool to functionalize the pyrrole nucleus
Cirrincione,Almerico,Passannanti,Diana,Mingoia
, p. 1169 - 1173 (2007/10/03)
Nucleophilic substitutions on halopyrroles by charged and neutral carbon, nitrogen, oxygen and sulfur nucleophiles are reported. Such reactions represent a valuable and versatile instrument to prepare a wide variety of functionalized pyrroles and to obtain building blocks for the synthesis of polycyclic systems.
