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Direct Asymmetric Reductive Amination for the Synthesis of (S)-Rivastigmine
In this article we demonstrate how asymmetric total synthesis of (S)-rivastigmine has been achieved using direct asymmetric reductive amination as the key transformation in four steps. The route started with readily available and cheap m-hydroxyacetophenone, through esterification, asymmetric reduct...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
MDPI
2018
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6225309/ https://www.ncbi.nlm.nih.gov/pubmed/30200331 http://dx.doi.org/10.3390/molecules23092207 |