Lapsley, Robert William (1940) A Study of the Active Esters of the Steroisomeric Mucic Acids in Relation to the Law of Optical Superposition. PhD thesis, University of Glasgow.
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Abstract
(1) Allomucic acid has been prepared from mucic acid and characterised. It has been found by Professor Posternak to be identical with his synthetic allomucic acid. (2) dl-Talomucic has been shown to rearrange in acetic anhydride to mucic acid and allomucic acid. A simple route is possibly available for synthesis of the ribose type of sugar structure. (3) The specific rotations of the 1-menthyl esters of tetra-acetyl mucic and tetra-acetyl allomucic acids have been compared. The specific rotations are not in agreement with van't Hoff's law of Optical Superposition. Additional Paper. (1) A synthetic route to 2.3.4.7-tetra methoxy 9 methyl phenanthrene has been extensively explored. (2) The stability of N-acetyl colchinol methyl ether to dehydrogenation has been further investigated and found to be in agreement with previous work. (3) Preliminary work on the synthesis of 2.3.4.6-tetra methoxy 9 methyl phenanthrene has been carried out. (4) Preliminary work has also been done on the synthesis of a possible simple analogue of colchinol methyl ether.
Item Type: | Thesis (PhD) |
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Qualification Level: | Doctoral |
Keywords: | Organic chemistry |
Date of Award: | 1940 |
Depositing User: | Enlighten Team |
Unique ID: | glathesis:1940-80222 |
Copyright: | Copyright of this thesis is held by the author. |
Date Deposited: | 02 Mar 2020 17:10 |
Last Modified: | 02 Mar 2020 17:10 |
URI: | https://theses.gla.ac.uk/id/eprint/80222 |
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