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Synthesis of an advanced intermediate en route to the mitomycin natural products
Authors:Williams Amie L  Srinivasan Jayasree M  Johnston Jeffrey N
Affiliation:Department of Chemistry, Vanderbilt University, Nashville, Tennessee 37235-1822, USA.
Abstract:[Structure: see text] An advanced intermediate in our planned synthesis of mitomycin C has been acquired in nine steps from tert-butyl glyoxylate. The aziridinyl pyrrolidine and quinone subunits are coupled regioselectively to arrive at an enamine that is prepared for C10 homologation.
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