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University of Illinois at Urbana-Champaign

The Alpha-Alkoxyallylation of Activated Carbonyl Compounds: A Novel Variant of the Michael Reaction

Abstract

dc:description

Five methods of alkoxyallylation at the alpha carbon of activated carbonyl compounds are proposed and explored. The product of alkoxyallylation, which are enol ethers, are protected equivalents of the adducts obtained from the Michael reaction of (alpha),(beta)-enals with activated carbonyl compounds.

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
2014

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Hobbs, Steven John

Subjects

dc:subject × 1

Identifiers

dc:identifier.*
Identifier
(UMI)AAI8324574
OAI identifier oai:identifier
oai:www.ideals.illinois.edu:2142/70220

Chain of custody

source
Harvested from
University of Illinois - Urbana-Champaign
Base URL
www.ideals.illinois.edu/oai-pmh
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
citation

Hobbs, Steven John. The Alpha-Alkoxyallylation of Activated Carbonyl Compounds: A Novel Variant of the Michael Reaction. Dissertation thesis, University of Illinois at Urbana-Champaign, 2014. http://hdl.handle.net/2142/70220