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.
| Identifer | oai:union.ndltd.org:unt.edu/info:ark/67531/metadc279187 |
| Date | 08 1900 |
| Creators | Skelton, Wm. Paul |
| Contributors | Skinner, Charles Gordon, Truitt, Price |
| Publisher | North Texas State University |
| Source Sets | University of North Texas |
| Language | English |
| Detected Language | English |
| Type | Thesis or Dissertation |
| Format | iv, 27 leaves: ill., Text |
| Rights | Public, Copyright, Copyright is held by the author, unless otherwise noted. All rights reserved., Skelton, Wm. Paul |
Page generated in 0.0024 seconds