- About
-
The Global ETD Search service is a free service for researchers
to find electronic theses and dissertations. This service is
provided by the
Networked Digital Library of Theses and Dissertations.
Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
Search results
Showing 31 to 40 of 81 (0.014 seconds)| 31 |
The interaction of sulphur dioxide with monoterpenesJohnson, T. J. January 1972 (has links)
No description available.
|
| 32 |
The synthesis and deamination of 4-, 7- and 10-aminopinanesWebb, T. C. January 1971 (has links)
No description available.
|
| 33 |
Studies on the synthesis and antiinflammatory properties of ring-D aminosteroidsGriggs, S. C. January 1978 (has links)
No description available.
|
| 34 |
A convergent approach to produce the basic skeleton of the marine natural product eleutherobin and analoguesTirnaveanu, A. E. January 2008 (has links)
Eleutherobin 1 was isolated in 1994 from the soft coral ofthe Elelltherobia species in Western Australia. E1eutherobin attracted interest as it showed in vitro cytotoxicity towards selected cancer cell lines. Due to the scarce availability of this exciting compound we proposed a convergent synthesis of eleutherobin believing that it would provide the necessary intermediates to scale up the production ofthis drug and analogues in order for the therapeutic activity to be investigated. In this project the formation of the basic skeleton of eleutherobin 1 was attempted, and the basic skeletons of two of its analogues (2 and 23). Molecules 1 and 2 are both diterpene glycosides, characterised by a fused tricyclic skeleton comprising six-, nine- and five membered rings, which are termed A, Band C respectively, with the difference in the substitution of C-4 position of ring C (1, R=' OMe, while 2, R= Me). Molecule 23 has the same structure as 2 with the difference that ring B has 10 carbon atoms. The formation of the so called 'northern' and 'southern' bonds of the basic skeleton of 1, 2 and 23 respectively remains at the basis of our convergent approach to the synthesis of eleutherobin 1 and its analogues 2 and 23. The identified key intermediates were successfully synthesised from the commercially available R-(-)-phellandrene and 2-methylfuran or 2,5-dimethylfuran respectively.
|
| 35 |
Preparation and properties of strained norbornane lactonesMcIntyre, D. J. January 1979 (has links)
No description available.
|
| 36 |
Synthesis of spiro [4.5] decane sesquiterpenesBuddhasukh, Duang January 1975 (has links)
No description available.
|
| 37 |
The Mechanism of the Barton ReactionSmith, L. C. January 1977 (has links)
No description available.
|
| 38 |
Studies in the SynThesis of PolyterpenoidsTillekeratne, L. M. V. January 1975 (has links)
No description available.
|
| 39 |
Studies in the terpenoid fieldLabbe, D. C. January 1979 (has links)
No description available.
|
| 40 |
Synthetic studies on gibberellinsLyall, W. J. S. January 1977 (has links)
No description available.
|
Page generated in 0.0381 seconds