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Studies Targeting Ryanodol Result in an Annulation Reaction for the Synthesis of a Variety of Fused Carbocycles
An annulation reaction is described to access a range of polycyclic and highly oxygenated carbocycles. First developed in an approach to the synthesis of ryanodol, metallacycle-mediated annulative diketone–alkyne coupling defines a framework for realization of new retrosynthetic relationships for co...
Tallennettuna:
| Julkaisussa: | Org Lett |
|---|---|
| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2019
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6677624/ https://ncbi.nlm.nih.gov/pubmed/31298546 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acs.orglett.9b02278 |
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