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Molecules 2003, 8(2), 251-255; doi:10.3390/80200251
Article

Regioselective Ethanolamination and Ketalization of 3-Ph-2,4-diacetyl(diethoxycarbonyl)-5-hydroxy-5-methylcyclohexanones

, ,  and *
Chair of Organic and Bioorganic Chemistry, Saratov State University, 83 Astrakhanskaya Str., Saratov 410026, Russia
* Author to whom correspondence should be addressed.
Received: 16 November 2002 / Revised: 24 January 2003 / Accepted: 26 January 2003 / Published: 28 February 2003
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Abstract

The reaction of 3-phenyl-2,4-diacetyl(diethoxycarbonyl)-5-hydroxy-5-methylcyclohexanones with ethanolamine and ethylene glycol proceeds regioselectively using the carbonyl group of the alicycle to produce the corresponding cyclohexenylethanolamines and dioxolanes.
Keywords: Cyclohexanones; ethanolamine; ethylene glycol; enaminoketones; heterospirans Cyclohexanones; ethanolamine; ethylene glycol; enaminoketones; heterospirans
This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).
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Kriven'ko, A.P.; Kozlova, E.A.; Grigor'ev, A.V.; Sorokin, V.V. Regioselective Ethanolamination and Ketalization of 3-Ph-2,4-diacetyl(diethoxycarbonyl)-5-hydroxy-5-methylcyclohexanones. Molecules 2003, 8, 251-255.

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