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University of Illinois at Urbana-Champaign
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
Abstract
dc:descriptionItem withdrawn by Mark Zulauf (zulauf@illinois.edu) on 2012-06-15T13:39:00Z Item was in collections: University of Illinois Theses & Dissertations (ID: 1) No. of bitstreams: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, checksum: 31badb7e58ce4065eade504990cfba74 (MD5)
Degree
thesis:*- Name thesis:degree_name
- Ph.D.
- Level thesis:degree_level
- Dissertation
- Discipline thesis:degree_discipline
- Chemistry
- Grantor
- University of Illinois at Urbana-Champaign
- Year dc:date
- 2012
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Burk, Matthew
- Contributors dc:contributor
-
- Denmark, Scott E.
- White, Maria C.
- van der Donk, Wilfred A.
- Rauchfuss, Thomas B.
Subjects
dc:subject × 34- enantioselective
- Halogenation
- chlorination
- bromination
- iodination
- chlorolactonization
- chloroetherification
- chlorocyloetherification
- bromolactonization
- bromoetherification
- bromocycloetherification
- iodolactonization
- iodoetherification
- iodocycloetherification
- halonium
- haliranium
- bromonium
- bromiranium
- chloronium
- chloriranium
- solvolysis
- racemization
- olefin-to-olefin transfer
- Lewis base
- chiral
- chiral Lewis base
- Lewis base catalysis
- Silicon tetrachloride
- silyl ketene imine
- aldol
- germanium
- crossed aldol
- kinetics
- chiral Bronsted acid
Rights
dc:rights- Statement dc:rights
-
- Copyright 2012 Matthew Burk
- Language dc:language
- en
Identifiers
dc:identifier.*- Handle dc:identifier
- http://hdl.handle.net/2142/34528
- OAI identifier oai:identifier
- oai:www.ideals.illinois.edu:2142/34528