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Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/75540
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dc.titleAldol reaction under solvent-free conditions: Highly stereoselective synthesis of 1,3-amino alcohols
dc.contributor.authorLoh, T.-P.
dc.contributor.authorHuang, J.-M.
dc.contributor.authorGoh, S.-H.
dc.contributor.authorVittal, J.J.
dc.date.accessioned2014-06-23T05:31:37Z
dc.date.available2014-06-23T05:31:37Z
dc.date.issued2000-05-04
dc.identifier.citationLoh, T.-P.,Huang, J.-M.,Goh, S.-H.,Vittal, J.J. (2000-05-04). Aldol reaction under solvent-free conditions: Highly stereoselective synthesis of 1,3-amino alcohols. Organic Letters 2 (9) : 1291-1294. ScholarBank@NUS Repository.
dc.identifier.issn15237060
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75540
dc.description.abstract(formula presented) A method for the highly stereoselective synthesis of 1,3-amino alcohols based on the indium trichloride-catalyzed Mukaiyama aldol reaction of keto ester (R,S)-1 under solvent-free conditions has been developed. The high selectivity observed can be explained on the basis of the shielding of one face by a remote substituent.
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.sourcetitleOrganic Letters
dc.description.volume2
dc.description.issue9
dc.description.page1291-1294
dc.identifier.isiutNOT_IN_WOS
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