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Synfacts 2011(11): 1198-1198
DOI: 10.1055/s-0031-1289185
DOI: 10.1055/s-0031-1289185
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag
Stuttgart ˙ New York
A One-Pot Synthesis of Challenging Chiral Primary Amines
T. C. Nugent*, D. E. Negru, M. El-Shazly, D. Hu, A. Sadiq, A. Bibi, M. N. Umar
Jacobs University Bremen, Germany
Weitere Informationen
Publikationsverlauf
Publikationsdatum:
19. Oktober 2011 (online)

Significance
The conventional synthetic methods for the synthesis of primary amines require multiple steps and harsh nitrogen deprotection conditions, which lead to low overall yield. The authors described a one-pot synthesis of chiral primary amines through an asymmetric reductive amination-hydrogenolysis sequence. In spite of their low reactivity, they achieved the synthesis of ortho-substituted phenylethyl amines in good yield and with high enantioselectivity.