Johnson-Claisen rearrangement

An allylic alcohol reacts with an orthoester under weak-acid catalysis to give a ketene acetal, which rearranges to an unsaturated ester.

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Past exam of the chemistry course of the year 3 of the natural sciences course of the University of Cambridge / 2022 / Paper 4 / 55 / a / iii / Solution
Past exam of the chemistry course of the year 3 of the natural sciences course of the University of Cambridge / 2022 / Paper 4 / 55 / a / i / Solution
Past exam of the chemistry course of the year 4 of the natural sciences course of the University of Cambridge / 2022 / Paper 2 / Section F / 29 / b / Solution

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