Synthesis 2013; 45(2): 153-166
DOI: 10.1055/s-0032-1317589
feature article
© Georg Thieme Verlag Stuttgart · New York

Step-Efficient Access to Chiral Primary Amines

Authors

  • Thomas C. Nugent*

    Department of Chemistry, School of Engineering and Science, Jacobs University Bremen, Campus Ring 1, 28759 Bremen, Germany   Fax: +49(421)2003229   Email: t.nugent@jacobs-university.de
  • Sofiya M. Marinova

    Department of Chemistry, School of Engineering and Science, Jacobs University Bremen, Campus Ring 1, 28759 Bremen, Germany   Fax: +49(421)2003229   Email: t.nugent@jacobs-university.de
Further Information

Publication History

Received: 02 October 2012

Accepted after revision: 23 October 2012

Publication Date:
02 January 2013 (online)


Graphical Abstract

Preview

Abstract

Routes to enantioenriched amines are outlined that employ reductive amination and carbanion addition methods. The strategies require either one or two reaction steps from prochiral carbonyl compounds for the synthesis of the corresponding chiral primary amines.