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

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

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

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MDPI and ACS Style

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.

AMA Style

Asmanidou A, Papoutsis I, Spyroudis S, Varvoglis A. Spiro Cyclohexadienones from the Reaction of Phenolic Enaminone Derivatives with Hypervalent Iodine Reagents. Molecules. 2000; 5(6):874-879.

Chicago/Turabian Style

Asmanidou, Anna; Papoutsis, Ioannis; Spyroudis, Spyros; Varvoglis, Anastasios. 2000. "Spiro Cyclohexadienones from the Reaction of Phenolic Enaminone Derivatives with Hypervalent Iodine Reagents." Molecules 5, no. 6: 874-879.

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