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Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/75480
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dc.titleA remote substituent as a control element in indium-mediated allylation reactions in aqueous media: Highly diastereoselective synthesis of 1,3-amino alcohols
dc.contributor.authorLoh, T.-P.
dc.contributor.authorHuang, J.-M.
dc.contributor.authorXu, K.-C.
dc.contributor.authorGoh, S.-H.
dc.contributor.authorVittal, J.J.
dc.date.accessioned2014-06-23T05:30:53Z
dc.date.available2014-06-23T05:30:53Z
dc.date.issued2000-08-12
dc.identifier.citationLoh, T.-P.,Huang, J.-M.,Xu, K.-C.,Goh, S.-H.,Vittal, J.J. (2000-08-12). A remote substituent as a control element in indium-mediated allylation reactions in aqueous media: Highly diastereoselective synthesis of 1,3-amino alcohols. Tetrahedron Letters 41 (33) : 6511-6515. ScholarBank@NUS Repository.
dc.identifier.issn00404039
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75480
dc.description.abstractA new method for the stereoselective synthesis of 1,3-amino alcohols based on the indium-mediated allylation of keto ester (R,S)-2 in aqueous media, resulting from shielding of one face by a remote substituent, was developed to be a useful method for acyclic stereocontrol in the absence of any obvious steric interaction. (C) 2000 Elsevier Science Ltd.
dc.sourceScopus
dc.subject1,3-amino alcohols
dc.subjectAllylation
dc.subjectHigh diastereoselectivity
dc.subjectIndium
dc.subjectRemote substituent
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.sourcetitleTetrahedron Letters
dc.description.volume41
dc.description.issue33
dc.description.page6511-6515
dc.description.codenTELEA
dc.identifier.isiutNOT_IN_WOS
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