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Conformational Analogs of Some Phytoactive Compounds

In an effort to determine if there is a specific conformational structure which is most effective at the appropriate active physiological site, the synthesis of a group of sterically restricted analogs was undertaken. A portion of the polymethylene carbon skeleton of glutaric acid was replaced by selected aromatic carbons in benzenedicarboxylic acids to produce a series of ridged conformers, and the relative plant growth regulating properties of these derivatives were determined.

Identiferoai:union.ndltd.org:unt.edu/info:ark/67531/metadc279187
Date08 1900
CreatorsSkelton, Wm. Paul
ContributorsSkinner, Charles Gordon, Truitt, Price
PublisherNorth Texas State University
Source SetsUniversity of North Texas
LanguageEnglish
Detected LanguageEnglish
TypeThesis or Dissertation
Formativ, 27 leaves: ill., Text
RightsPublic, Copyright, Copyright is held by the author, unless otherwise noted. All rights reserved., Skelton, Wm. Paul

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