Spiro Cyclohexadienones from the Reaction of Phenolic Enaminone Derivatives with Hypervalent Iodine Reagents
Abstract
:Introduction
Results and Discussion
Conclusion
Experimental
Typical procedure for the preparation of 5 and 9
2-Methyl-3-carboxyethyl-1,4,5,6-tetrahydropyridino-4-spiro-4'-cyclohexa-2',5'-dien-1'-one 5a
2-Phenyl-3-carboxyethyl-1,4,5,6-tetrahydropyridino-4-spiro-4'-cyclohexa-2',5'-dien-1'-one 5b
7,7-Dimethyl-1,2,3,4,5,6,7,8-octahydro-quinoline-5-one-4-spiro-4'-cyclohexa-2',5'-dien-1'-one 9
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- Samples Availability: Not available.
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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. https://doi.org/10.3390/50600874
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. https://doi.org/10.3390/50600874
Chicago/Turabian StyleAsmanidou, Anna, Ioannis Papoutsis, Spyros Spyroudis, and Anastasios Varvoglis. 2000. "Spiro Cyclohexadienones from the Reaction of Phenolic Enaminone Derivatives with Hypervalent Iodine Reagents" Molecules 5, no. 6: 874-879. https://doi.org/10.3390/50600874