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New methods for medium ring synthesis: Towards the total synthesis of clavirolide B

Posted on:2007-08-31Degree:Ph.DType:Thesis
University:Boston CollegeCandidate:White, Brian HFull Text:PDF
GTID:2451390005486138Subject:Chemistry
Abstract/Summary:
Chapter 1. Review of the use of cyclobutenes in the total synthesis of natural products.; Chapter 2. Presentation of a methodology for the synthesis of bicyclic medium ring systems by ring-closing/ring-opening olefin metathesis followed by oxy-Cope rearrangement.*; Chapter 3. Efforts toward the total synthesis of the dolabellane diterpene clavirolide B utilizing an intermolecular Lewis-acid catalyzed cycloaddition, an intermolecular [2+2] photocycloaddition, and thermal fragmentation of the resulting photoadduct.*; *Please refer to dissertation for diagrams.
Keywords/Search Tags:Total synthesis
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