Eschenmoser–Claisen rearrangement

E398759 UNEXPLORED

The Eschenmoser–Claisen rearrangement is a variant of the Claisen rearrangement in organic chemistry that converts allylic alcohols and amides into γ,δ-unsaturated carbonyl compounds via a [3,3]-sigmatropic rearrangement.


Referenced by (1)
Subject (surface form when different) Predicate
Albert Eschenmoser
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