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

Adele P. Kriven'ko, Eleanor A. Kozlova, Alexander V. Grigor'ev and Vitaly V. Sorokin* email
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; in revised form: 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

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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.

AMA Style

Kriven'ko AP, Kozlova EA, Grigor'ev AV, Sorokin VV. Regioselective Ethanolamination and Ketalization of 3-Ph-2,4-diacetyl(diethoxycarbonyl)-5-hydroxy-5-methylcyclohexanones. Molecules. 2003; 8(2):251-255.

Chicago/Turabian Style

Kriven'ko, Adele P.; Kozlova, Eleanor A.; Grigor'ev, Alexander V.; Sorokin, Vitaly V. 2003. "Regioselective Ethanolamination and Ketalization of 3-Ph-2,4-diacetyl(diethoxycarbonyl)-5-hydroxy-5-methylcyclohexanones." Molecules 8, no. 2: 251-255.

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