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Enantioselective synthesis of polyhydroxyindolizidinone and quinolizidinone derivatives from a common precursor
A concise asymmetric synthetic route to two new tetrahydroxyindolizidinone and quinolizidinone derivatives has been developed from a common intermediate which featured a highly selective dihydroxylation reaction and a RCM reaction as key steps.
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| Publicado no: | Beilstein J Org Chem |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Beilstein-Institut
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4311665/ https://ncbi.nlm.nih.gov/pubmed/25670979 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3762/bjoc.10.327 |
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