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The acid catalysed equilibration of 4-alkylcyclohex-3-enones and 4-alkyl-cyclohex-2-enones.

✍ Scribed by K.G. Lewis; G.J. Williams


Book ID
104240390
Publisher
Elsevier Science
Year
1965
Tongue
French
Weight
184 KB
Volume
6
Category
Article
ISSN
0040-4039

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✦ Synopsis


The acid or base catalysed conversion of a non-conjugated unsaturated carbonyl compound into the conjugated isomer has been frequently used in synthetic procedures. There have been various reports of reactions where the conversion was incomplete or even where no rearrangement appeared to occur (1). As part of a survey of the acid catalysed rearrangement of a series of unsaturated cyclic ketones we have examined the following equilibrium. k--(--)=0 H'_ R-o (I) (II)


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The Beckmann Rearrangement of Cyclohex-2-enone Oximes. Synthesis of 4, 5-Diphenyl-2,3,4,5-tetrahydro-1H-azepin-2-one. -The title compound (VI), which is an intermediate for the preparation of certain pesticides, can be prepared from both isomeric oximes (IV) and (V). In contrast, only the syn oxime