Please use this identifier to cite or link to this item:
|Title:||Asymmetric catalysis with chiral primary amine-based organocatalysts||Authors:||Xu, L.-W.
|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|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.