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Total Synthesis of ent-Plagiochianin B
[Image: see text] An enantioselective total synthesis of plagiochianin B is described that employs (+)-3-carene as its point of departure and delivers the enantiomer of the natural product. Key features of the synthesis include a palladium-mediated regioselective oxidative cleavage of an olefin resi...
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| Vydáno v: | Org Lett |
|---|---|
| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Chemical Society
2021
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| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7901668/ https://ncbi.nlm.nih.gov/pubmed/33517659 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acs.orglett.0c04219 |
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