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

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

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Received: 6 May 2000; Accepted: 25 May 2000 / Published: 9 June 2000
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.
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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