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Kolarovic, A., Kaslin, A. and Wennemers, H. (2014) Stereoselective Synthesis of Indolines via Organocatalytic Thioester Enolate Addition Reactions. Organic Letters, 1616, 4236-4239. https://doi.org/10.1021/ol501936n

has been cited by the following article:

• TITLE: An Efficient Synthesis of Enantiomerically Pure γ-Aminobutyric Acid (GABA) Derivatives

  AUTHORS: Huixia Liu, Jiani Yuan, Qinqin Tian, Nan Ji, Wei He

  KEYWORDS: Chiral, GABA, Organocatalyst, Asymmetric Michael Addition

  JOURNAL NAME: Journal of Materials Science and Chemical Engineering, Vol.5 No.8, August 11, 2017

  ABSTRACT: Chiral γ-aminobutyric acid (GABA) derivatives are the normal inhibitory neurotransmitters in the mammalian central nervous system. In this paper, enantiopure GABA derivatives 6 were synthesized via reduction/cyclization/hydrolysis cascade reactions from the highly enantioselective β-aryl-γ- ni-troalkanes Michael adducts 4, which was obtained from asymmetric Michael addition of S, S’-diphenyldithiomalonate 2 to trans-β-nitroolefins 1, using novel chiral cinchona alkaloid-derived thioureas 3 as the organocatalysts. This synthesis represents an efficient, highly selective and environmental benign methodology for GABA derivatives.