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Virginia Tech

Determination of the relative stereochemistry of adducts resulting from the addition lithium dienolates to Michael acceptors

Abstract

dc:description.abstract

The addition of the lithium dienolate of ethyl crotonate to 2-cyclopentenone was studied to determine the stereochemical outcome of this Michael addition. Proof of the stereochemistry was provided via the unambiguous synthesis and comparison of ketone 73 from norcamphor 85.

Degree

thesis:*
Name thesis:degree_name
Master of Science
Level thesis:degree_level
masters
Discipline thesis:degree_discipline
Chemistry
Department dc:contributor.department
Chemistry
Grantor dc:publisher
Virginia Tech
Year dc:date.issued
1994

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • McLamore, Dolores Sherita

Rights

dc:rights
Statement dc:rights
  • In Copyright
Language dc:language.iso
en

Identifiers

dc:identifier.*
Dc Identifier Other
etd-06112009-063224
OAI identifier oai:identifier
oai:vtechworks.lib.vt.edu:10919/43137

Chain of custody

source
Harvested from
Virginia Tech
Base URL
vtechworks.lib.vt.edu/oai/request
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
related terms
citation

McLamore, Dolores Sherita. Determination of the relative stereochemistry of adducts resulting from the addition lithium dienolates to Michael acceptors. masters thesis, Virginia Tech, 1994. http://hdl.handle.net/10919/43137