Synlett 1997; 1997(1): 29-30
DOI: 10.1055/s-1997-715
letter
© 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.

Reversal of Chemoselectivity in Organotin Lewis Acid-Catalyzed Reaction of Ketene Silyl Acetal with Aldehyde and α-Enal

Jianxie Chen, Junzo Otera*
  • *Department of Applied Chemistry, Okayama University of Science, Ridai-cho, Okayama 700, Japan
Weitere Informationen

Publikationsverlauf

Publikationsdatum:
22. März 2004 (online)

The organotin Lewis acid-catalyzed reaction of ketene silyl acetal with aldehydes results in reversal of chemoselectivity: α-enals react preferentially or exclusively in competition with an alkanal or even aromatic aldehydes.