The algar–flynn–oyamada oxidation of α-substituted chalcones

Autor: T. P. Lavin, D. P. Melody, E. M. Philbin, A. K. Keenan, D. M. X. Donnelly, W. P. Cullen
Rok vydání: 1971
Předmět:
Zdroj: J. Chem. Soc. C. :2848-2855
ISSN: 0022-4952
DOI: 10.1039/j39710002848
Popis: 2-(α-Hydroxybenzyl)-2-methoxycoumaran-3-ones are major products in the alkaline hydrogen peroxide oxidation (AFO reaction) of 2′-hydroxy-α-methoxychalcones containing a phloroglucinol type A-ring, while flavonols predominate in the oxidation products of chalcones without a 6′-substituent. Under similar oxidation conditions, α-methyl substituted chalcones give corresponding results. Stereochemistry is assigned to the 3-methylflavan-3-ols on the basis of chemical and n.m.r. evidence.
Databáze: OpenAIRE