The absolute configurations of vicinal diols

Pipithakul, Thuanthong

Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/127177

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DC Field	Value	Language
dc.contributor.advisor	Hamon, D.P.G.	-
dc.contributor.advisor	Massy-Westropp, R.A.	-
dc.contributor.author	Pipithakul, Thuanthong	-
dc.date.issued	1974	-
dc.identifier.uri	http://hdl.handle.net/2440/127177	-
dc.description.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..	en
dc.language.iso	en	en
dc.title	The absolute configurations of vicinal diols	en
dc.type	Thesis	en
dc.contributor.school	School of Chemistry and Physics : Chemistry	en
dc.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	en
dc.description.dissertation	Thesis (M.Sc.)--University of Adelaide, Dept. of Organic Chemistry, 1975	en
Appears in Collections:	Research Theses

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