Abstract
A total synthesis of (+)-galanthamine [(+)-1] has been achieved using the readily available and enantiomerically pure metabolite 2 as starting material. The quaternary carbon centre (C8a) associated with target 1 was constructed using the EschenmoserClaisen rearrangement reaction.
| Original language | English |
|---|---|
| Pages (from-to) | 1437-1447 |
| Number of pages | 11 |
| Journal | Australian Journal of Chemistry |
| Volume | 63 |
| Issue number | 10 |
| DOIs | |
| Publication status | Published - 2010 |
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