Determining the structures of halogenated marine natural products by total synthesis
<p>Elatenyne, a brominated C<sub>15</sub> acetogenin isolated from the red <em>Laurencia elata</em> marine algae, was originally assigned a pyranopyran structure. Previous total synthesis of the pyranopyran structure has found this assignment to be incorrect. During thi...
المؤلف الرئيسي: | Dyson, BS |
---|---|
مؤلفون آخرون: | Burton, J |
التنسيق: | أطروحة |
اللغة: | English |
منشور في: |
2011
|
الموضوعات: |
مواد مشابهة
-
Studies towards the total synthesis of manzamine A
حسب: Hawkins, A
منشور في: (2013) -
The synthesis and biology of iminosugars and their precursors
حسب: Ayers, B, وآخرون
منشور في: (2014) -
Total synthesis of (–)-nakadomarin A and an approach to the diazatricyclic core of the madangamines
حسب: Kyle, A
منشور في: (2012) -
Asymmetric synthesis of piperidine alkaloids
حسب: Thomson, A, وآخرون
منشور في: (2012) -
Palladium-catalysed cascade cyclisation of alkynyl silanes and studies towards rubriflordilactone A
حسب: Cordonnier, M, وآخرون
منشور في: (2011)