Cyclopentenoid Cyanogens: Their Chemistry, Importance in Plant Systematics, and Their Role in the Coevolution of Plants and Insects (Phytochemistry, Cyanogenic, Glycosides, Nmr)
Spencer, Kevin C.
This item is only available for download by members of the University of Illinois community. Students, faculty, and staff at the U of I may log in with your NetID and password to view the item. If you are trying to access an Illinois-restricted dissertation or thesis, you can request a copy through your library's Inter-Library Loan office or purchase a copy directly from ProQuest.
Permalink
https://hdl.handle.net/2142/71279
Description
Title
Cyclopentenoid Cyanogens: Their Chemistry, Importance in Plant Systematics, and Their Role in the Coevolution of Plants and Insects (Phytochemistry, Cyanogenic, Glycosides, Nmr)
Author(s)
Spencer, Kevin C.
Issue Date
1984
Department of Study
Plant Biology
Discipline
Plant Biology
Degree Granting Institution
University of Illinois at Urbana-Champaign
Degree Name
Ph.D.
Degree Level
Dissertation
Keyword(s)
Biology, Botany
Abstract
Cyanogenic glycosides containing a cyclopentene ring were investigated chemically. Techniques for their isolation from plant sources were devised, and data accumulated on their spectroscopic properties. The distribution of cyclopentenoid cyanogens in plants was investigated, and it was determined that members of the Passifloraceae, Turneraceae, Malesherbiaceae, Flacourtiaceae and Caricaceae elaborate these compounds. The value of such a distribution in assessing taxonomic relationships was tested numerically in one genus. Cyclopentenoid cyanogens were found to be useful indicators of phylogenetic affinity at all taxonomic levels. A correlation was discovered between the pattern of elaboration of plant cyclopentenoid compounds and the host-plant preference of Heliconiine butterflies in their coevolutionary interaction with species in the genus Passiflora. A number of new structures are described for cyclopentenoid cyanogenic glycosides isolated from natural sources. An investigation into the biological activity of these compounds showed several to possess potential antitumor activity.
Use this login method if you
don't
have an
@illinois.edu
email address.
(Oops, I do have one)
IDEALS migrated to a new platform on June 23, 2022. If you created
your account prior to this date, you will have to reset your password
using the forgot-password link below.