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Please use this identifier to cite or link to this item: http://hdl.handle.net/10198/828

Título: Synthesis of the first thieno-δ-carboline. Fluorescence studies in solution and in lipid vesicles
Autor: Queiroz, Maria João R.P.
Castanheira, Elisabete M.S.
Pinto, Ana M.R.
Ferreira, Isabel C.F.R.
Begouin, Agathe
Kirsch, Gilbert
Palavras-chave: Palladium-assisted reactions
Thieno-δ-carboline
Fluorescence
Solvatochromic probes
Lipid vesicles
Issue Date: 2006
Editora: Elsevier
Citação: Journal of Photochemistry and Photobiology A: Chemistry. ISSN 1010-6030. 181:2-3 (2006) p. 290-296
Resumo: The first thieno-δ-carboline (6,8,9-trimethyl-5H-pyrido[3,2-b]thieno[3,2-f]indole) was prepared in good yield (70%) by intramolecular palladium-assisted cyclization of an ortho-chlorodiarylamine. The latter was in turn selectively synthesized in high yield (90%) by C–N palladiumcatalyzed cross-coupling of 3-bromo-2-chloropyridine with, the also prepared, 6-amino-2,3,7-trimethylbenzo[b]thiophene. Fluorescence studies in solution show that thieno-δ-carboline has a solvatochromic behaviour. Despite the low fluorescence quantum yields in solution, studies of its incorporation in lipid vesicles of DPPC, DOPE and DODAB indicate that thienocarboline is located mainly inside the lipid bilayer, exhibiting different behaviours in gel or liquid-crystalline phases. Our studies are useful for the incorporation of thienocarboline in liposomes and for controlled drug release assays, due to its biological activity.
URI: http://hdl.handle.net/10198/828
ISSN: 1010-6030
Appears in Collections:BB - Artigos em Revistas Indexados ao ISI

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