Abstract
A convenient reaction sequence in which the key step is a Stevens rearrangement, leading to dimethyl ethers of 5-n-alkylresorcinols has been developed and exemplified by the synthesis of the dimethyl ethers of the natural phenols, dihydropersoonol, grevillol, and bilobol. The tetramethyl ether of bis-norstriatol was also synthesized by the same route.
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