- Highly enantioselective transfer hydrogenation of fluoroalkyl ketones.
Highly enantioselective transfer hydrogenation of fluoroalkyl ketones.
Organic letters (2006-12-15)
Damjan Sterk, Michel Stephan, Barbara Mohar
PMID17165898
ZUSAMMENFASSUNG
[Structure: see text] The asymmetric transfer hydrogenation of fluoroalkyl ketones mediated by [Ru(eta6-arene)((S,S)-R2NSO2DPEN)] catalysts using HCO2H-Et3N afforded the corresponding alcohols with high ee's and in excellent yields.
MATERIALIEN
Produktnummer
Marke
Produktbeschreibung
Sigma-Aldrich
Di-μ-chloro-dichloro-bis-[(1,2,3,4,5,6-η)-1,3,5-trimethylbenzol]-diruthenium, 95%