Abstract
A pyrroloindolizidine skeleton, which is observed in myrmicarin alkaloids isolated from African ant, is highly unique, oligocyclic indolizidine derivative. We describe here an attempt on a synthesis of a pyrroloindolizidine skeleton with our originally developed gold-catalyzed cascade reaction and a newly developed synthetic route for the skeleton via gold-catalyzed hydroamination-enamine cyclization-ring-closing metathesis.
Original language | English |
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Pages (from-to) | 875-890 |
Number of pages | 16 |
Journal | Heterocycles |
Volume | 99 |
Issue number | 2 |
DOIs | |
State | Published - 2019 |
ASJC Scopus subject areas
- Analytical Chemistry
- Pharmacology
- Organic Chemistry