Russian Journal of Organic Chemistry

Acid hydrolysis of amides obtained by Beckmann rearrangement of methyl ketones oximes of unsaturated γ-lactone, aromatic, and alicyclic series

GG Tokmadzhyan

Index: Tokmadzhyan Russian Journal of Organic Chemistry, 2011 , vol. 47, # 11 p. 1746 - 1749

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Citation Number: 1

Abstract

Abstract Beckmann rearrangement was performed of oximes of substituted 3-acetyl-4-methyl- 5, 5-dimethyl (pentamethylene)-2-oxo-2, 5-dihydrofuranes in the presence of boron trifluoride etherate. Aiming at establishing the spatial arrangement of the oximes the hydrolysis was carried out of acid amides obtained by Beckmann rearrangement of oximes of methyl ketones belonging to unsaturated γ-lactone series and also to aromatic and ...

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