Loading...
A stereoselective synthesis of (+)-boronolide
A stereoselective synthesis of (+)-boronolide is described. The key steps involve a stereoselective reduction of an α-hydroxy ketone, allylation of an α-hydroxy aldehyde and a ring-closing olefin metathesis of a homoallylic alcohol derived acrylate ester utilizing Grubbs’ catalyst.
Na minha lista:
| Udgivet i: | Tetrahedron Lett |
|---|---|
| Main Authors: | , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2000
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6234978/ https://ncbi.nlm.nih.gov/pubmed/30449906 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/S0040-4039(99)02246-7 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|