Research output: Contribution to Journal/Magazine › Journal article › peer-review
| <mark>Journal publication date</mark> | 26/10/2006 |
|---|---|
| <mark>Journal</mark> | Organic Letters |
| Issue number | 22 |
| Volume | 8 |
| Number of pages | 4 |
| Pages (from-to) | 5145-5148 |
| Publication Status | Published |
| <mark>Original language</mark> | English |
A new three-step route to azaspirocycles involving the organolithium-mediated conversion of beta-alkoxy aziridines into substituted cyclopentenyl amines, hydroboration, and cyclization has been developed. The methodology is utilized in the construction of the pentacyclic ring system of cephalotaxine.