https://search.dev.ndltd.org/etd/uiuc/oai:www.ideals.illinois.edu:2142/34528
type: CreativeWork
name: 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
description: Item withdrawn by Mark Zulauf (zulauf@illinois.edu) on 2012-06-15T13:39:00Z Item was in collections: University of Illinois Theses & Dissertations (ID: 1) No. of bitstreams: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, checksum: 31badb7e58ce4065eade504990cfba74 (MD5)
abstract: Item withdrawn by Mark Zulauf (zulauf@illinois.edu) on 2012-06-15T13:39:00Z Item was in collections: University of Illinois Theses & Dissertations (ID: 1) No. of bitstreams: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, checksum: 31badb7e58ce4065eade504990cfba74 (MD5)
author: Burk, Matthew
language: en
keywords: 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
date published: 2012-09-18T21:24:13Z
date modified: 2026-07-22T22:25:31Z
provider: University of Illinois - Urbana-Champaign
publisher: Networked Digital Library of Theses and Dissertations
type: WebPage
source organization: University of Illinois at Urbana-Champaign

PropertyValue
property ID: Handle
value: http://hdl.handle.net/2142/34528