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 |
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Pages (from-to) | 1437-1447 |
Number of pages | 11 |
Journal | Australian Journal of Chemistry |
Volume | 63 |
Issue number | 10 |
DOIs | |
Publication status | Published - 2010 |