Please use this identifier to cite or link to this item: https://doi.org/10.1039/b821070e
Title: Asymmetric catalysis with chiral primary amine-based organocatalysts
Authors: Xu, L.-W. 
Luo, J.
Lu, Y. 
Issue Date: 2009
Citation: Xu, L.-W., Luo, J., Lu, Y. (2009). Asymmetric catalysis with chiral primary amine-based organocatalysts. Chemical Communications (14) : 1807-1821. ScholarBank@NUS Repository. https://doi.org/10.1039/b821070e
Abstract: In the past few years, primary amine catalysts derived from natural amino acids, Cinchona alkaloids and other chiral amines have emerged as readily available, highly versatile and extremely powerful catalysts in asymmetric synthesis. They have been demonstrated to be effective catalysts in a wide range of enantioselective organic reactions. In comparison with secondary amine-mediated transformations, the use of primary amine organocatalysts has often been shown to be complementary or superior. © 2009 The Royal Society of Chemistry.
Source Title: Chemical Communications
URI: http://scholarbank.nus.edu.sg/handle/10635/75616
ISSN: 13597345
DOI: 10.1039/b821070e
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