Download PDF
Synthesis 1990; 1990(9): 815-816
DOI: 10.1055/s-1990-27023
paper
© 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.

Hydroborations: A New Efficient Route to 1-Organo-2-indanones from 1-Alkyl(aryl)indenes

B. S. Kirkiacharian* , P. G. Koutsourakis
  • *Laboratoire de Chimie Thérapeutique, Faculté de Pharmacie de Paris-Sud, 5, rue J. B. Clément, F-92296-Chatenay-Malabry Cedex, France
Further Information

Publication History

Publication Date:
17 September 2002 (online)

  PDF Download  Permissions and Reprints All articles of this category

The hydroboration followed by chromic acid oxidation leads in the cases of 1-alkyl- and 1-aryl-1-indenes to the corresponding 1-organo-2-indanones in 70-80% yield.

      >