Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/75480
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. 
Huang, J.-M.
Xu, K.-C.
Goh, S.-H. 
Vittal, J.J. 
Keywords: 1,3-amino alcohols
Allylation
High diastereoselectivity
Indium
Remote substituent
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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