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Molecules 2000, 5(6), 874-879; doi:10.3390/50600874
Article

Spiro Cyclohexadienones from the Reaction of Phenolic Enaminone Derivatives with Hypervalent Iodine Reagents

, , *  and
Laboratory of Organic Chemistry, Chemistry Department, University of Thessaloniki, Thessaloniki 54006, Greece
* Author to whom correspondence should be addressed.
Received: 6 May 2000 / Accepted: 25 May 2000 / Published: 9 June 2000
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Abstract

Phenolic enamino compounds, prepared from 2-(4-hydroxyphenyl)-ethylamine and the corresponding β-keto carbonyl compounds, afford spiro cyclohexadienone derivatives on reaction with hypervalent iodine reagents.
Keywords: Spiro cyclohexadienones; hypervalent iodine; enamino esters Spiro cyclohexadienones; hypervalent iodine; enamino esters
This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).
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Asmanidou, A.; Papoutsis, I.; Spyroudis, S.; Varvoglis, A. Spiro Cyclohexadienones from the Reaction of Phenolic Enaminone Derivatives with Hypervalent Iodine Reagents. Molecules 2000, 5, 874-879.

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