Please use this identifier to cite or link to this item: https://doi.org/10.1002/adsc.200600564
Title: Highly efficient threonine-derived organocatalysts for direct asymmetrie aldol reactions in water
Authors: Wu, X. 
Jiang, Z.
Shen, H.-M. 
Lu, Y. 
Keywords: Aldol reaction
Asymmetric catalysis
Hydrophobic effect
Organic catalysis
Water
Issue Date: Apr-2007
Source: Wu, X., Jiang, Z., Shen, H.-M., Lu, Y. (2007-04). Highly efficient threonine-derived organocatalysts for direct asymmetrie aldol reactions in water. Advanced Synthesis and Catalysis 349 (6) : 812-816. ScholarBank@NUS Repository. https://doi.org/10.1002/adsc.200600564
Abstract: The introduction of siloxy groups at the hydroxy function of natural threonine resulted in efficient hydrophobic organocatalysts, which could efficiently catalyze the direct aldol reactions of both cyclic and acyclic ketones with aromatic aldehydes in water with excellent enantiomeric excess. © 2007 Wiley-VCH Verlag GmbH & Co. KGaA,.
Source Title: Advanced Synthesis and Catalysis
URI: http://scholarbank.nus.edu.sg/handle/10635/76300
ISSN: 16154150
DOI: 10.1002/adsc.200600564
Appears in Collections:Staff Publications

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