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Issue 2, 1987
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A short, general, organoselenium-mediated synthesis of cyclic acetals

Abstract

Readily available substrates containing a strategically placed carbonyl group and two isolated double bonds can be coaxed into cyclic acetal formation in a single step employing phenylselenenyl chloride in aqueous acetonitrile.

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Article information


J. Chem. Soc., Chem. Commun., 1987, 78-80
Article type
Paper

A short, general, organoselenium-mediated synthesis of cyclic acetals

G. Mehta, H. S. P. Rao and K. R. Reddy, J. Chem. Soc., Chem. Commun., 1987, 78
DOI: 10.1039/C39870000078

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