Lataa...
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.
Tallennettuna:
| Julkaisussa: | Beilstein J Org Chem |
|---|---|
| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Beilstein-Institut
2014
|
| Aiheet: | |
| Linkit: | 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 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|