Resumen
A general study of the enantioselective protonation of prochiral enolates with 2-sulfinyl alcohols is reported. The modification of reaction conditions to reduce drastically the amount of chiral proton source needed to obtain a good enantiomeric excess is reported. The effects of the different factors controlling the stereoselectivity are clearly established. Different protocols for enolate generation are compared.
| Idioma original | Inglés |
|---|---|
| Páginas (desde-hasta) | 266-286 |
| Número de páginas | 21 |
| Publicación | Arkivoc |
| Volumen | 2005 |
| N.º | 9 |
| DOI | |
| Estado | Publicada - 8 abr 2005 |
| Publicado de forma externa | Sí |
Huella
Profundice en los temas de investigación de 'From over-stoichiometric to sub-stoichiometric enantioselective protonation with 2-sulfinyl alcohols: A view in perspective'. En conjunto forman una huella única.Cómo citar
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