Repository logo
 
No Thumbnail Available
Publication

Synthesis of potential anti-tumoral ring a substituted tieno[3,2-c]carbazoles from diarylamines

Use this identifier to reference this record.
Name:Description:Size:Format: 
Int_8.pdf657.14 KBAdobe PDF Download

Advisor(s)

Abstract(s)

Thienocarbazoles bearing electron donating or withdrawing groups in ring a, were prepared by intramolecular oxidative cyclization of diarylamines using stoichiometric or catalytic Pd(OAc)2 amounts, in fair to moderate yields. ln the latter case Cu(OAch was added to reoxidize Pd(O) forrned. The diarylamine precursors were prepared by palladium-catalysed amination.

Description

Keywords

Citation

Ferreira, Isabel C.F.R.; Queiroz, Maria-João R.P.; Kirsch, Gilbert (2002). Synthesis of potential anti-tumoral ring a substituted tieno[3,2-c]carbazoles from diarylamines. In XXth European Colloqium on Heterocyclic Chemistry. Estocolmo

Research Projects

Organizational Units

Journal Issue