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Progress Toward the Total Synthesis of Bielschowskysin: A Stereoselective [2+2] Photocycloaddition
[Image: see text] The tetracyclic core of the diterpene bielschowskysin has been prepared as a single enantiomer via astereoselective intramolecular [2+2] photocycloaddition of 5-alkylidene-2(5H)-furanone 3.
Tallennettuna:
| Päätekijät: | , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2006
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2527052/ https://ncbi.nlm.nih.gov/pubmed/16494470 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol0530225 |
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