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09:08
From a Natural Product to Its Biosynthetic Gene Cluster: A Demonstration Using Polyketomycin from Streptomyces diastatochromogenes Tü6028
Published on: January 13, 2017
Synthesis of an advanced intermediate en route to the mitomycin natural products
Amie L Williams1, Jayasree M Srinivasan, Jeffrey N Johnston
1Department of Chemistry, Vanderbilt University, Nashville, Tennessee 37235-1822, USA.
Organic Letters
|December 15, 2006
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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