Abstract
A short and efficient synthesis of (+)-1-hydroxyquinolizidinone as an advanced core intermediate for the syntheses of (+)-epiquinamide, (+)-homopumiliotoxin, and (+)-lupinine is described. The key feature of our strategy includes a sequential chiral transfer using an achiral phenylsulfide auxiliary via microwave-accelerated aza-Claisen rearrangement of the unexplored N-thiophenoxyacetyl-α-vinyl piperidine substrate and the oxone-induced transannulation.
Original language | English |
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Pages (from-to) | 4813-4815 |
Number of pages | 3 |
Journal | Tetrahedron Letters |
Volume | 53 |
Issue number | 36 |
DOIs | |
State | Published - 5 Sep 2012 |
Keywords
- (+)-1-Hydroxyquinolizidinone
- Achiral auxiliary
- aza-Claisen rearrangement
- Quinolizidine alkaloid
- Transannulation