Abstract
An efficient synthetic route to the spirally fused AG-ring model of pinnatoxin A has been devised using the intramolecular cyclization of epoxy nitrile followed by an aza-Wittig reaction to form a seven-membered cyclic imine.
Original language | English |
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Pages (from-to) | 891-893 |
Number of pages | 3 |
Journal | Synlett |
Issue number | 6 |
Publication status | Published - 2003 May 26 |
Keywords
- Alkylation
- Aza-Wittig reaction
- Cyclic imine
- Pinnatoxi A
- Spiro ring
ASJC Scopus subject areas
- Organic Chemistry