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Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.tetlet.2010.02.044
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dc.titleDirect asymmetric aldol reaction of acetone with α-ketoesters catalyzed by primary-tertiary diamine organocatalysts
dc.contributor.authorJiang, Z.
dc.contributor.authorLu, Y.
dc.date.accessioned2014-06-23T05:36:39Z
dc.date.available2014-06-23T05:36:39Z
dc.date.issued2010-04-07
dc.identifier.citationJiang, Z., Lu, Y. (2010-04-07). Direct asymmetric aldol reaction of acetone with α-ketoesters catalyzed by primary-tertiary diamine organocatalysts. Tetrahedron Letters 51 (14) : 1884-1886. ScholarBank@NUS Repository. https://doi.org/10.1016/j.tetlet.2010.02.044
dc.identifier.issn00404039
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75948
dc.description.abstractNovel primary-tertiary diamine organocatalysts derived from l-serine were utilized to promote enantioselective aldol reaction of acetone with α-ketoesters. The desired products were obtained in high yields and with good to excellent enantioselectivities (up to 95% ee). © 2010 Elsevier Ltd. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.tetlet.2010.02.044
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1016/j.tetlet.2010.02.044
dc.description.sourcetitleTetrahedron Letters
dc.description.volume51
dc.description.issue14
dc.description.page1884-1886
dc.description.codenTELEA
dc.identifier.isiut000275920600019
Appears in Collections:Staff Publications

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