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dc.contributor.advisorTimothy F. Jamison.en_US
dc.contributor.authorMorten, Christopher J. (Christopher John)en_US
dc.contributor.otherMassachusetts Institute of Technology. Dept. of Chemistry.en_US
dc.date.accessioned2011-08-18T19:11:35Z
dc.date.available2011-08-18T19:11:35Z
dc.date.copyright2011en_US
dc.date.issued2011en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/65271
dc.descriptionThesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2011.en_US
dc.descriptionVita. Cataloged from PDF version of thesis.en_US
dc.descriptionIncludes bibliographical references.en_US
dc.description.abstractChapter I. Introduction to the Ladder Polyethers. We introduce the bioactivity of the ladder polyether natural products and provide an overview of the puzzle that is their biogenesis. Cascades of endo-selective epoxide opening inspired by the biosynthetic proposal and promoted by simple neutral water can provide efficient access to these compounds. Chapter II. Water-Promoted Epoxide Opening Accommodates Methyl Substitution. ... Methyl (Me) substitution poses a challenge to the achievement of endo-selective epoxide-opening cascades, as these groups can direct the regioselectivity of epoxide opening. Water as reaction solvent and promoter overcomes such directing effects and enables the incorporation of proximally Me-substituted epoxides into endo-selective cascades. However, Me-substituted epoxides do reduce the overall efficiency of cascades. Chapter III. Kinetics of an Epoxide-Opening Cascade Promoted by Neutral Water. Evidence for a Stepwise Mechanism. ... Detailed investigation of the kinetics of an endo-selective epoxide-opening cascade in water reveals a stepwise mechanism, not a concerted one. While the first step proceeds with poor rate and selectivity, the second cyclization, which is templated by a fused THP diad, proceeds with excellent endo selectivity. Chapter IV. Preliminary Investigation of a Dioxane Template for Endo-Selective Epoxide-Opening Cyclization. ... Use of a 1,3-dioxane as template ring, a methylene acetal engenders endoselective epoxide opening under both acidic and basic conditions. Cyclization in neutral water proceeds with superb endo selectivity. Chapter V. Progress Toward the Synthesis of Gambierol via Endo-Selective Epoxide-Opening Cascades Promoted by Water. ... We report progress toward the biomimetic total synthesis of the ladder polyether gambierol. The FGH ring system has been synthesized in a 20 step longest linear sequence, via an endo-selective epoxide-opening cascade promoted by water. Chapter VI. Conclusion: Potential Implications of the Foregoing Work on the Biosynthesis of the Ladder Polyethers. We summarize lessons learned from in vitro emulation of the hypothesized biosynthesis of the ladder polyethers and speculate on the possibility of ring junction methylation subsequent to the epoxide-opening cascade step.en_US
dc.description.statementofresponsibilityby Christopher J. Morten.en_US
dc.format.extent433 p.en_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsM.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582en_US
dc.subjectChemistry.en_US
dc.titleEndo-selective epoxide-opening cascades in wateren_US
dc.typeThesisen_US
dc.description.degreePh.D.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistry
dc.identifier.oclc743789658en_US


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