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Synfacts 2006(12): 1253-1253
DOI: 10.1055/s-2006-955643
DOI: 10.1055/s-2006-955643
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag Stuttgart · New York
Asymmetric Preparation of anti-β-Hydroxyα-amino Acid Esters
K. Makino, M. Iwasaki, Y. Hamada*
Chiba University, Japan
Weitere Informationen
Publikationsverlauf
Publikationsdatum:
22. November 2006 (online)


Significance
A cationic Ir(I) complex was used to effect the anti-selective hydrogenation of α-amino-β-keto esters via dynamic kinetic resolution (DKR) under mild conditions. The authors reported on new conditions for their previously developed system for the same reaction (K. Makino, Y. Hiroki, Y. Hamada J. Am. Chem. Soc. 2005, 127, 5784-5785). Now, using a cationic Ir(I) catalyst, yields were increased by ˜20% for all tested substrates and enantioselectivity was slightly increased in some cases. Another advantage is that the cationic catalyst allowed hydrogenation under 4.5 atm H2 instead of the previously reported 100 atm.