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Please use this identifier to cite or link to this item: https://doi.org/10.1002/adsc.200600564
DC FieldValue
dc.titleHighly efficient threonine-derived organocatalysts for direct asymmetrie aldol reactions in water
dc.contributor.authorWu, X.
dc.contributor.authorJiang, Z.
dc.contributor.authorShen, H.-M.
dc.contributor.authorLu, Y.
dc.date.accessioned2014-06-23T05:41:05Z
dc.date.available2014-06-23T05:41:05Z
dc.date.issued2007-04
dc.identifier.citationWu, X., Jiang, Z., Shen, H.-M., Lu, Y. (2007-04). Highly efficient threonine-derived organocatalysts for direct asymmetrie aldol reactions in water. Advanced Synthesis and Catalysis 349 (6) : 812-816. ScholarBank@NUS Repository. https://doi.org/10.1002/adsc.200600564
dc.identifier.issn16154150
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/76300
dc.description.abstractThe introduction of siloxy groups at the hydroxy function of natural threonine resulted in efficient hydrophobic organocatalysts, which could efficiently catalyze the direct aldol reactions of both cyclic and acyclic ketones with aromatic aldehydes in water with excellent enantiomeric excess. © 2007 Wiley-VCH Verlag GmbH & Co. KGaA,.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/adsc.200600564
dc.sourceScopus
dc.subjectAldol reaction
dc.subjectAsymmetric catalysis
dc.subjectHydrophobic effect
dc.subjectOrganic catalysis
dc.subjectWater
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.contributor.departmentCOMMUNITY,OCCUPATIONAL & FAMILY MEDICINE
dc.description.doi10.1002/adsc.200600564
dc.description.sourcetitleAdvanced Synthesis and Catalysis
dc.description.volume349
dc.description.issue6
dc.description.page812-816
dc.description.codenJPCHF
dc.identifier.isiut000246040000005
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