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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 |
| Appears in Collections: | Staff Publications |
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