C-ACYLATION OF AZOMETHINE GROUP IN O-BENZYL AROMATIC ALDOXIMES
Reaction of four O-benzyl aromatic aldoximes with phthalimidoacetyl chloride, 3,5-dinitrobenzoyl chloride or phthalimidoacetic-p-toluenesulfonyl anhydride in the presence of triethylamine afforded moderate yields of C-acylation products of the azomethine group.Mechanism of the reaction is discussed.
Baranowski, Andrzej
p. 1993 - 1998
(2007/10/02)
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