DOI:
10.1055/s-00000084
Synthesis
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References
This synthesis was previously reported.14f A study of the Claisen rearrangement of the allyloxybenzaldehyde intermediate concluded that the desired rearranged product 6 is obtained in low yield (15%). The main product of the reaction was 2-allyl-6-methoxyphenol, a consequence of the most favorable pathway of the process, which is a decarbonylation reaction followed by the Claisen rearrangement. See: Kilenyi SN. Mahaux JM. Van Durme E.
J. Org. Chem. 1991;
56: 2591
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