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University of Illinois at Urbana-Champaign

Rearrangements of 1-Heterosubstituted Chrysanthemyl Aldehyde and Chrysanthemyl Amines

Abstract

dc:description

One theory concerning the mechanism for the conversion of presqualene pyrophosphate to squalene involves postulation of a new intermediate (known locally as protosqualene pyrophosphate) which is a ring expanded analog of presqualene pyrophosphate. There is no direct evidence for this discrete new intermediate but a successful synthesis of it would facilitate, via biosynthetic incorporation studies, determination of whether or not such an intermediate does exist. With this goal in mind, research was undertaken to ascertain the feasibility of protosqualene pyrophosphate synthesis.

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
  • Vancantfort, Christopher Kent

Subjects

dc:subject × 1

Rights

Language dc:language
eng

Identifiers

dc:identifier.*
Identifier
(UMI)AAI8108693
OAI identifier oai:identifier
oai:www.ideals.illinois.edu:2142/67253

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

Vancantfort, Christopher Kent. Rearrangements of 1-Heterosubstituted Chrysanthemyl Aldehyde and Chrysanthemyl Amines. Dissertation thesis, University of Illinois at Urbana-Champaign, 2014. http://hdl.handle.net/2142/67253