By palladium catalysis substituted ortho‐iodoanisoles (5, 8, 10, 13) are transformed either to annulated pyran (6) or furan derivatives (7, 9, 11, 14, 15), depending on the reactivity of additional substituents. The regiochemistry of the domino coupling processes is analyzed and a mechanistic rationale developed. Key step is the CH activation at methoxy groups.
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Gerald Dyker (1994) studied this question.
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