Resum
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 | Anglès |
|---|---|
| Pàgines (de-a) | 266-286 |
| Nombre de pàgines | 21 |
| Revista | Arkivoc |
| Volum | 2005 |
| Número | 9 |
| DOIs | |
| Estat de la publicació | Publicada - 8 d’abr. 2005 |
| Publicat externament | Sí |
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