Synthesis 1988; 1988(8): 616-619
DOI: 10.1055/s-1988-27654
communication
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Synthesis of 1,1-Bis(seleno)-2-alkenes

R. Dieden* , L. Hevesi
  • *Department of Chemistry, Facultés Universitaires Notre-Dame de la Paix, 61, rue de Bruxelles, B-5000 Namur, Belgium
Further Information

Publication History

Publication Date:
20 August 2002 (online)

The success of the direct conversion of α,β-unsaturated carbonyl compounds into the corresponding diselenoacetals by means of selenol/zinc chloride or tris(seleno)borane greatly depends on the starting carbonyl derivative. Enals and cyclic enones are transformed most efficiently, whereas acyclic enones mainly produce 1,4-addition compounds.

    >