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Showing 1 to 2 of 2 for “"chlorolactonization"”.

  1. Organoselenium redox-catalyzed, enantioselective syn-difunctionalization of alkenes

    … the products obtained in both dichlorination and chlorolactonization might have been the consequence of Dynamic Kinetic Asymmetric Transformations (DyKAT), wherein the relative rates of displacement of selenium from diastereomeric resting state intermediates by chloride determined the final …

    uiuc Repository record for Organoselenium redox-catalyzed, enantioselective syn-difunctionalization of alkenes (opens in a new tab)

  2. Asymmetric Lewis base catalysis: I. Lewis base catalyzed halogenation and development of an enantioselective bromocycloetherification reaction; II. enantioselective addition of silyl ketene imines to carbonyl electrophiles

    Item withdrawn by Mark Zulauf (zulauf@illinois.edu) on 2012-06-15T13:39:00Z Item was in collections: University of Illinois Theses & Dissertations (ID: 1) No. of bitstreams: 2 Thesis-6-12.docx: 11084823 bytes, checksum: 0609048b408ae3adf1f485e3a9dde5d3 (MD5) Burk_Matthew.pdf: 14255171 bytes, …

    uiuc Repository record for Asymmetric Lewis base catalysis: I. Lewis base catalyzed halogenation and development of an enantioselective bromocycloetherification reaction; II. enantioselective addition of silyl ketene imines to carbonyl electrophiles (opens in a new tab)