- Highly enantioselective asymmetric hydrogenation of beta-acetamido dehydroamino acid derivatives using a three-hindered quadrant rhodium catalyst.
Highly enantioselective asymmetric hydrogenation of beta-acetamido dehydroamino acid derivatives using a three-hindered quadrant rhodium catalyst.
Organic letters (2004-09-25)
He-Ping Wu, Garrett Hoge
PMID15387569
ZUSAMMENFASSUNG
[reaction: see text] A previously reported three-hindered quadrant chiral ligand and its corresponding rhodium complex provide high enantioselectivity for the asymmetric hydrogenation of beta-acetamido dehydroamino acid substrates. Both (E)- and (Z)-substrates are hydrogenated with high enantioselectivity in all of the reported examples. Asymmetric hydrogenation of a cyclic beta-acetamido dehydroamino acid substrate in 85% ee is also reported.
MATERIALIEN
Produktnummer
Marke
Produktbeschreibung
Sigma-Aldrich
R-(tert-Butylmethylphosphino-di-tert-butylphosphinomethan)-η4-(1,5-Cyclooctadien)rhodium(I)-Tetrafluorborat, 96%