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Updated: Feb 11, 2026

Enzymatic Cascade Reactions for the Synthesis of Chiral Amino Alcohols from L-lysine
Published on: February 16, 2018
New Chiral Ligands with Nonstereogenic Chirotopic Centers for Asymmetric Synthesis
Claus-Dieter Graf1, Christophe Malan1, Paul Knochel1
1Fachbereich Chemie der Universität, Hans-Meerwein-Strasse, D-35032 Marburg (Germany), Fax: (+49) 6421-28-21-89.
Abstract:
Pseudo-C2 -symmetrical ligands have been prepared efficiently: The attachment of the chiral alkyl group to the heteroatom (P or N) through a nonstereogenic, chirotopic carbon center facilitates their synthesis as the configuration at this carbon atom no longer needs to be controlled. Two such ligands were combined, for example, in the base 1, which is especially useful for asymmetric deprotonation of prochiral ketones [Eq. (a)].
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