Abstract
Indospicine is a non-proteogenic amino acid that accumulates as the free amino acid in livestock grazing Indigofera plant species and causes both reproductive losses and hepatotoxic effects. An efficient synthetic route to l-indospicine from l-homoserine lactone is described. The methodology is applicable for the synthesis of both deuterium labelled isotopomers and structural analogues for utilisation in biological studies. The key steps are a zinc mediated Barbier reaction with acrylonitrile and a Pinner reaction that together introduce the target amidine moiety.
| Originalsprog | Engelsk |
|---|---|
| Tidsskrift | Organic & Biomolecular Chemistry |
| Vol/bind | 14 |
| Udgave nummer | 28 |
| Sider (fra-til) | 6826-6832 |
| Antal sider | 7 |
| ISSN | 1477-0520 |
| DOI | |
| Status | Udgivet - 2016 |
| Udgivet eksternt | Ja |
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