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Virginia Polytechnic Institute and State University

Synthesis and rearrangements of vinylcyclopropanes in a [2+3] cyclopentene and oxycyclopentene annulation methodology approach to (-)- specionin

Abstract

dc:description.abstract

The addition of lithium dienolate 130, formed from ethyl 2-bromocrotonate, to enones and aldehydes yielding vinylcyclopropanes and vinyloxiranes was optimized. Various methods, pyrolytic and nonpyrolytic, were examined for the rearrangement of the resulting vinylcyclopropanes to cyclopentenes in an overall [2+3] annulation sequence. During the course of these studies, a new rearrangement pathway of these vinylcyclopropanes to bridged [3.2.n] bicyclic systems was discovered thus establishing a new [3+4] annulation technology. The extension of the [2+3] annulation technology to oxygenated cyclopentanoids was addressed. Several ethyl 2-bromo-4-oxycrotonates were synthesized, and the reaction of their lithium dienolates (217) with enones was investigated. The rearrangement of the resulting enol ether terminated vinylcyclopropanes to oxygenated cyclopentenes was also examined. [see document for diagram of chemical reaction] The application of this methodology was expressed in a synthetic approach to (-)-specionin (109). The key steps in this synthesis involved the cyclopropanation of optically pure enone 147 with Iithium dienolate 155 to give vinylcyclopropanes 169-exo/endo and the rearrangement of 169 to the oxygenated cyclopentanoid 187-exo which possesses the correct stereochemistry for further elaboration to epoxy acetate 216, an intermediate in a reported synthesis of specionin. [see document for diagrams of chemical reactions]

Degree

thesis:*
Name thesis:degree_name
Ph. D.
Level thesis:degree_level
doctoral
Discipline thesis:degree_discipline
Chemistry
Department dc:contributor.department
Chemistry
Grantor dc:publisher
Virginia Polytechnic Institute and State University
Year dc:date.issued
1989

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Fleming, Alison A.
Chair dc:contributor.committeechair
  • Hudlicky, Tomas
Committee members dc:contributor.committeemember
  • Wolfe, James F.
  • Mason, John G.
  • Tanko, James M.
  • White, Robert H.

Rights

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

Identifiers

dc:identifier.*
Handle dc:identifier.uri
http://hdl.handle.net/10919/54358
OAI identifier oai:identifier
oai:vtechworks.lib.vt.edu:10919/54358

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

Fleming, Alison A.. Synthesis and rearrangements of vinylcyclopropanes in a [2+3] cyclopentene and oxycyclopentene annulation methodology approach to (-)- specionin. doctoral thesis, Virginia Polytechnic Institute and State University, 1989. http://hdl.handle.net/10919/54358