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Fukuyama, Tohru Linsell, Martin Sheringham 2009-06-04T00:10:15Z 2009-06-04T00:10:15Z 1994 Linsell, Martin Sheringham. "Synthesis of optically pure mitomycin C: A new route to FR900482." (1994) Master’s Thesis, Rice University. <a href="https://hdl.handle.net/1911/13860">https://hdl.handle.net/1911/13860</a>. https://hdl.handle.net/1911/13860 THESIS CHEM. 1994 LINSELL Optically pure mitomycin C was synthesized in 28 steps and 5% overall yield from 2,6-dimethoxytoluene. The route followed was a variation upon previous work in our laboratories and the asymmetry was achieved by the resolution of racemic mitomycin A, an advanced intermediate. Our efforts at finding a new route to an intermediate in the synthesis of FR900482, are also described here. The key step was the cyclization of an epoxy-acetamide under basic conditions to form an eight-membered lactam. 140 p. application/pdf eng Copyright is held by the author, unless otherwise indicated. Permission to reuse, publish, or reproduce the work beyond the bounds of fair use or other exemptions to copyright law must be obtained from the copyright holder. Organic chemistry Synthesis of optically pure mitomycin C: A new route to FR900482 Thesis Text Chemistry Natural Sciences Rice University Masters Master of Arts open.access