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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 which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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MDPI and ACS Style

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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