ja106088v_si_002.cif (20.65 kB)

Bispalladacycle-Catalyzed Brønsted Acid/Base-Promoted Asymmetric Tandem Azlactone Formation−Michael Addition

Download (20.65 kB)
dataset
posted on 08.09.2010, 00:00 by Manuel Weber, Sascha Jautze, Wolfgang Frey, René Peters
Cooperative activation by a soft bimetallic catalyst, a hard Brønsted acid, and a hard Brønsted base has allowed the formation of highly enantioenriched, diastereomerically pure masked α-amino acids with adjacent quaternary and tertiary stereocenters in a single reaction starting from racemic N-benzoylated amino acids. The products can, for example, be used to prepare bicyclic dipeptides.

History