Abstract
A bidirectional synthesis of the originally proposed structures for the natural products elatenyne and a chloroenyne from Laurencia majuscula is described along with a reassessment of the structures of the halogenated enynes based upon a C-13 NMR chemical shift/structure correlation.
Original language | English |
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Pages (from-to) | 238-252 |
Number of pages | 15 |
Journal | Organic and Biomolecular Chemistry |
Volume | 7 |
Issue number | 2 |
Early online date | 20 Nov 2008 |
DOIs | |
Publication status | Published - 2009 |
Keywords
- supramolecular host systems
- 2-directional chain synthesis
- natural product syntheses
- fused polycyclic ethers