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Obtention de selenopysultones lors de l'oxydation de thio-1 chromenes par le dioxyde de selenium
Authors:J. Van Coppenolle  M. Renson
Affiliation:Institut de Chimie Organique, Université de Liège, 1 Bis, quai Roosevelt, 4000 Liege, Belgique
Abstract:
Selenium dioxide oxidation of 1-thiochromene leads to 3-formyl (5,6)benzo-1,2 thiaseleninne-1,1-dioxide, which is a representative of a hitherto unknown class of heterocyclic compounds. Pyrolysis of this compound leads to 2-formyl benzo(b)selenophen, by loss of sulphur dioxide. The reaction can be applied to other 1 thiochromenes but no similar behaviour has been observed for their selenium isologues.
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