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Issue 6, 1979
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One step synthesis of octalones or indanones by Friedel–Crafts acylation

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 type: Paper
DOI: 10.1039/C39790000263
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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