Resumen
The ethyl carbamate of norpandamarilactonine-A was prepared in an enantiomerically pure form starting from (S)-prolinol, Deprotection of the amine functionality rendered both diastereomeric norpandamarilactonines as racemates, which were used as synthetic precursors of pandamarilactonine-A and -B. © Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.
| Idioma original | Inglés |
|---|---|
| Páginas (desde-hasta) | 48-53 |
| Publicación | European Journal of Organic Chemistry |
| N.º | 1 |
| DOI | |
| Estado | Publicada - 1 ene 2004 |
Huella
Profundice en los temas de investigación de 'Synthetic Studies on Pandanus Alkaloids: From Norpandamarilactonines to Pandamarilactonines, a Proof of Their Configurational Instability'. En conjunto forman una huella única.Citar esto
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver