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A concise Diels–Alder strategy leading to congeners of the ABC ring system of the marine alkaloid ‘upenamide
A second-generation approach to the BC spirocycle of ‘upenamide is reported. Central to the synthesis is an endo selective Diels–Alder reaction between 1-(t-butyldimethylsiloxy)-1,3-butadiene and bromomaleic anhydride followed by a radical mediated allylation of the ring fusion bromide. Functional g...
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| Publicado no: | Tetrahedron Lett |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8023302/ https://ncbi.nlm.nih.gov/pubmed/33828342 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tetlet.2016.05.102 |
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