This
study reveals an alternative
sequence for the synthesis of compounds that contain the pyrrolodiketopiperazine
structural motif. Starting with a diketopiperazine precursor, a mild
aldol condensation precedes pyrrole annulation and bicyclic ring fusion.
The derived intermediate aldol condensation products, which bear either
a protected carbonyl or a functionalized alkyne, can be cyclized to
the pyrrolodiketopiperazine by protic or gold Lewis acid catalysis.
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