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University of Illinois at Urbana-Champaign
Synthesis and Claisen Rearrangement of Alpha-Ethoxyallyl Vinyl Ethers. Evidence for a Dipolar Transition State
Abstract
dc:descriptionThe product stereoselectivity, scope, and mechanism of the Claisen-Micheal reaction (8 $\rightarrow$ 11) were explored. The products (e.g. 11) of the Claisen-Micheal reaction, which are enol ethers, are protected equivalents of the adducts obtained from the Micheal reaction of α,β-enals with activated carbonyl compounds.$$\vbox{\vskip72pt}$$==>>>
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
- 1987
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Rogers, Brian Daniel
Subjects
dc:subject × 1Identifiers
dc:identifier.*- Identifier
- (UMI)AAI8721744
- OAI identifier oai:identifier
- oai:www.ideals.illinois.edu:2142/70379