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Beckmann rearrangement

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Beckmann Rearrangement

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Beckmann rearrangement

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Beckmann Rearrangement Example Mechanism | Organic Chemistry

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Beckmann Rearrangement Mechanism | Organic Chemistry

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Beckmann Rearrangement

The Beckmann rearrangement, named after the German chemist Ernst Otto Beckmann (1853–1923), is a rearrangement of an oxime functional group to substituted amides. The rearrangement has also been successful performed on haloimines and nitrones. Cyclic oximes and haloimines yield lactams.
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