Please use this identifier to cite or link to this item: https://doi.org/10.1039/b713151h
Title: Bicyclic guanidine-catalyzed enantioselective phospha-Michael reaction: Synthesis of chiral β-aminophosphine oxides and β-aminophosphines
Authors: Fu, X. 
Jiang, Z. 
Tan, C.-H. 
Issue Date: 2007
Citation: Fu, X., Jiang, Z., Tan, C.-H. (2007). Bicyclic guanidine-catalyzed enantioselective phospha-Michael reaction: Synthesis of chiral β-aminophosphine oxides and β-aminophosphines. Chemical Communications (47) : 5058-5060. ScholarBank@NUS Repository. https://doi.org/10.1039/b713151h
Abstract: Chiral bicyclic guanidine has been found to catalyze the phospha-Michael reactions of diaryl phosphine oxide to nitroalkenes with high enantioselectivities, offering a direct methodology to prepare chiral β-aminophosphine oxides and β-aminophosphines. © The Royal Society of Chemistry.
Source Title: Chemical Communications
URI: http://scholarbank.nus.edu.sg/handle/10635/93168
ISSN: 13597345
DOI: 10.1039/b713151h
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