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X. Xu, S. R. S. Saibabu Kutti, J. Liv, J. F. Cannon, A. D. Headly and G. Li, “Ionic Liquid Media Resulted in the First Asymmetric Aminohalogenation Reaction of Alkenes” Organic Letters, Vol. 6, No. 26, 2004, pp. 4881-4884. doi:10.1021/ol048045i

has been cited by the following article:

• TITLE: Asymmetric Reductive Amination of Carbonyl Compounds by Using N,N,N-Tributylpropanaminium Based Novel Chiral Ionic Liquid

  AUTHORS: Boyina Rupini, Sharda Pasricha, Brijesh Rathi

  KEYWORDS: Ionic Liquid; Asymmetric Reductive Amination; Chiral; Carbonyl Compounds

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.3 No.3, August 29, 2013

  ABSTRACT: Asymmetric reductive amination of carbonyl compounds was carried out using a novel class of aliphatic quarternary ammonium based chiral ionic liquid. S-(+)-2,3-dihydroxy-N,N,N-tributylpropanaminum bromide chiral ionic liquid has been synthesized, characterized and used for asymmetric reductive amination of carbonyl compounds in the presence of sodium borohydride. These preliminary results are encouraging and advocate dual role of novel ionic liquid as a medium and reducing agent for proficient conversion of ketones to amines, however, reductive amination reaction needs to be established for other substituents.