Abstract:The approach towards the total synthesis of MPC1001 is based on disconnections across the dioxopiperazine and the diaryl ether subunit of MPC1001 utilizing a late‐stage construction of the oxepin ring via the highly substituted pyrrolidine (IV), which in turn is accessible by a novel asymmetric dipolar cycloaddition methodology involving substrates (I), (II), and (III).
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