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Un Nouveau type d'ouverture de sélénophénes condensés
Authors:FB Iteke  L Christiaens  M Renson
Institution:Institut de Chimie Organique, Université de Liége, 1 bis, quai Roosevelt, 4000 Liege, Belgium
Abstract:A condensed selenophene ring can be opened by selenium-metal interconversion, when the selenium atom is α to a five-membered aromatic ring, as in selenopheno 2,3-b] thiophene. In tricyclic compounds bearing 2,3-b] condensed triophene and selenophene rings, the selenophene ring open, whether in central or in lateral positions. When the tricyclic compound bears two 2,3-b] condensed selenophene rings, only the central selenophene ring opens by interconversion. Corresponding 3,2-b]isomers do not undergo this ring opening.
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