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                <term xml:lang="en">diarylheptanoid</term>
                <term xml:lang="en">natural product</term>
                <term xml:lang="en">macrocycle</term>
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              <p>A convergent approach for the synthesis of (±)-myricanol, a strained diarylheptanoid isolated from Myricacae, was undertaken using a Suzuki-Miyaura coupling followed by a RCM. Herein, we report the unintentional formation of a 26-membered macrocycle as RCM product resulting from a head-to-tail dimerization of the seco-precursor, even in RRCM conditions.</p>
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