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Please use this identifier to cite or link to this item: https://doi.org/10.1039/b706793c
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dc.titleHighly diastereoselective and enantioselective direct organocatalytic anti-selective Mannich reactions employing N-tosylimines
dc.contributor.authorCheng, L.
dc.contributor.authorHan, X.
dc.contributor.authorHuang, H.
dc.contributor.authorWong, M.W.
dc.contributor.authorLu, Y.
dc.date.accessioned2014-06-23T05:41:04Z
dc.date.available2014-06-23T05:41:04Z
dc.date.issued2007
dc.identifier.citationCheng, L., Han, X., Huang, H., Wong, M.W., Lu, Y. (2007). Highly diastereoselective and enantioselective direct organocatalytic anti-selective Mannich reactions employing N-tosylimines. Chemical Communications (40) : 4143-4145. ScholarBank@NUS Repository. https://doi.org/10.1039/b706793c
dc.identifier.issn13597345
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/76299
dc.description.abstractOrganocatalytic direct anti-selective Mannich reactions of O-TBS-hydroxyacetone with various N-tosylimines derived from aromatic aldehydes in the presence of L-threonine-derived catalyst afforded 1,2-amino alcohols in good yields and with enantioselectivities of 99% in almost all cases. © The Royal Society of Chemistry.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/b706793c
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/b706793c
dc.description.sourcetitleChemical Communications
dc.description.issue40
dc.description.page4143-4145
dc.description.codenCHCOF
dc.identifier.isiut000250085500019
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