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