The stereochemistry of enamide intermediates in DuPHOS-Rh(I) catalysed asymmetric hydrogenation
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference12 articles.
1. Asymmetric hydrogenation of methyl (Z)-.alpha.-acetamidocinnamate catalyzed by [1,2-bis(phenyl-o-anisoyl)phosphino)ethane]rhodium(I): kinetics, mechanism and origin of enantioselection
2. The catalytic resting state of asymmetric homogeneous hydrogenation. Exchange processes delineated by nuclear magnetic resonance saturation-transfer (DANTE) techniques
3. Iridium complexes of dehydroamino acids: The kinetic resolution of racemic diphosphines and their application in catalytic asymmetric hydrogenation
4. Catalyst-substrate adducts in asymmetric catalytic hydrogenation. Crystal and molecular structure of rhodium [((R,R)-1,2-bis{phenyl-o-anisoylphosphino}ethane)(methyl (Z)-.beta.-propyl-.alpha.-acetamidoacrylate)] tetrafluoroborate [Rh(DIPAMP)(MPAA)]BF4
5. Identification of the enantioselective step in the asymmetric catalytic hydrogenation of a prochiral olefin
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