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|Title:||A remote substituent as a control element in indium-mediated allylation reactions in aqueous media: Highly diastereoselective synthesis of 1,3-amino alcohols||Authors:||Loh, T.-P.
|Issue Date:||12-Aug-2000||Citation:||Loh, 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.||Abstract:||A 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.||Source Title:||Tetrahedron Letters||URI:||http://scholarbank.nus.edu.sg/handle/10635/75480||ISSN:||00404039|
|Appears in Collections:||Staff Publications|
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