Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/127177
Type: Thesis
Title: The absolute configurations of vicinal diols
Author: Pipithakul, Thuanthong
Issue Date: 1974
School/Discipline: School of Chemistry and Physics : Chemistry
Abstract: Some optically active vicinal diols of known absolute configurations were synthsised. The application of Horeau's method for the determination of the absolute configurations of these diols were found to be valid. The method has been used to determine the absolute configuration of alternifolenediol of previously unknown configuration. Preliminary studies for the conversion of 3-ethylidene 2,2,4,4-tetramethylcyclobutanol, a chiral molecule, into a vicinal diol by stereo-chemically defined processes is reported..
Advisor: Hamon, D.P.G.
Massy-Westropp, R.A.
Dissertation Note: Thesis (M.Sc.)--University of Adelaide, Dept. of Organic Chemistry, 1975
Provenance: This electronic version is made publicly available by the University of Adelaide in accordance with its open access policy for student theses. Copyright in this thesis remains with the author. This thesis may incorporate third party material which has been used by the author pursuant to Fair Dealing exceptions. If you are the owner of any included third party copyright material you wish to be removed from this electronic version, please complete the take down form located at: http://www.adelaide.edu.au/legals
Appears in Collections:Research Theses

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