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Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/76311
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dc.titleHighly stereoselective indium trichloride-catalysed asymmetric aldol reaction of formaldehyde and a glucose-derived silyl enol ether in water
dc.contributor.authorLoh, T.-P.
dc.contributor.authorChua, G.-L.
dc.contributor.authorVittal, J.J.
dc.contributor.authorWong, M.-W.
dc.date.accessioned2014-06-23T05:41:13Z
dc.date.available2014-06-23T05:41:13Z
dc.date.issued1998-04-21
dc.identifier.citationLoh, T.-P.,Chua, G.-L.,Vittal, J.J.,Wong, M.-W. (1998-04-21). Highly stereoselective indium trichloride-catalysed asymmetric aldol reaction of formaldehyde and a glucose-derived silyl enol ether in water. Chemical Communications (8) : 861-862. ScholarBank@NUS Repository.
dc.identifier.issn13597345
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/76311
dc.description.abstractThe yield and stereochemical outcome of the reaction between D-glucose-derived silyl enol ether 1 (Z and E isomers) and commercial formaldehyde in water catalysed by indium(III) choride was studied.
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.sourcetitleChemical Communications
dc.description.issue8
dc.description.page861-862
dc.description.codenCHCOF
dc.identifier.isiutNOT_IN_WOS
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