Issue 6, 1979
From the journal:

Journal of the Chemical Society, Chemical Communications

One step synthesis of octalones or indanones by Friedel–Crafts acylation

Zoubida Bounkhala,   Salih Hacini,   Roselyne Pardo  and  Maurice Santelli  

Abstract

Acylation of cyclohexene (or cyclopentene) by vinylacetyl bromide in the presence of AlCl3 gave a mixture of the octalones (or indanones)(3) and the propenyl cyclohexenyl (or cyclopentenyl) ketones (4).

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Article information

DOI
https://doi.org/10.1039/C39790000263
Article type
Paper

J. Chem. Soc., Chem. Commun., 1979, 263-263

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One step synthesis of octalones or indanones by Friedel–Crafts acylation

Z. Bounkhala, S. Hacini, R. Pardo and M. Santelli, J. Chem. Soc., Chem. Commun., 1979, 263 DOI: 10.1039/C39790000263

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