Please use this identifier to cite or link to this item: https://doi.org/10.1039/b713151h
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dc.titleBicyclic guanidine-catalyzed enantioselective phospha-Michael reaction: Synthesis of chiral β-aminophosphine oxides and β-aminophosphines
dc.contributor.authorFu, X.
dc.contributor.authorJiang, Z.
dc.contributor.authorTan, C.-H.
dc.date.accessioned2014-10-16T08:21:11Z
dc.date.available2014-10-16T08:21:11Z
dc.date.issued2007
dc.identifier.citationFu, 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
dc.identifier.issn13597345
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/93168
dc.description.abstractChiral 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.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/b713151h
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/b713151h
dc.description.sourcetitleChemical Communications
dc.description.issue47
dc.description.page5058-5060
dc.description.codenCHCOF
dc.identifier.isiut000251336600024
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