| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5215849 | Tetrahedron | 2014 | 10 Pages |
Abstract
A variety of novel 2,5-diaryl-indolizines have been prepared through the palladium-catalyzed cross-coupling reactions of organozinc reagents prepared from 2-aryl-indolizines with aromatic halides. The photophysical properties of representative compounds indicate that the 2,5-diaryl-indolizines are promising candidates to be used in optoelectronic devices and biomolecular labeling. In addition, cyclic voltammetry studies of some nitrophenyl-substituted indolizines have shown evidences of an oxidation process without the correspondent reduction peak suggesting a dimerization reaction.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Mônica F.Z.J. Amaral, Laila A. Deliberto, Camila R. de Souza, Rose M.Z.G. Naal, Zeki Naal, Giuliano C. Clososki,