Abstract
A short and cost-effective synthesis of the important strigolactone analogue (+)-GR24 is described. Central to this new approach is the concise, enantioselective synthesis of the A-C ring system.
| Original language | English |
|---|---|
| Pages (from-to) | 1516 - 1520 |
| Number of pages | 5 |
| Journal | The Journal of Organic Chemistry |
| Volume | 79 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - 17 Jan 2014 |
| Externally published | Yes |
Keywords
- enantioselective synthesis
- strigolactone
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Third-Generation Light-Driven Symmetric Molecular Motors
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From chaos to order: Chain-length dependence of the free energy of formation of meso-tetraalkylporphyrin self-assembled monolayer polymorphs
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Reimers, J. R., Panduwinata, D., Visser, J., Tang, C., Goerigk, L., Ford, M. J., Sintic, M., Sum, T.-J., Coenen, M. J. J., Hendriksen, B. L. M., Elemans, J. A. A. W., Hush, N. S. & Crossley, M. J., 28 Oct 2015, In: Proceedings of the National Academy of Sciences. 112, 45, p. E6101 - E6110 10 p.Research output: Contribution to journal › Article › Academic › peer-review
Open Access
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