The Journal of Organic Chemistry

Carbon acidity. 79. Acidity of enolate equivalent compounds: oxime ethers

JC Ciula, A Streitwieser

Index: Ciula, James C.; Streitwieser, Andrew Journal of Organic Chemistry, 1991 , vol. 56, # 6 p. 1989 - 1993

Full Text: HTML

Citation Number: 7

Abstract

Results The oxime ethers were prepared by condensation of the appropriate ketone with methoxylamine hydrochloride in ethanol/pyridine solvent (5050). 12 Ketones were prepared with chromophoric groups attached to the carbonyl moiety (1-5) so that the carbanions from the derived oxime ethers