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|Title:||Bicyclic guanidine-catalyzed enantioselective phospha-Michael reaction: Synthesis of chiral β-aminophosphine oxides and β-aminophosphines||Authors:||Fu, X.
|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|
|Appears in Collections:||Staff Publications|
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